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<!--
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||
UID=101799
|
||
ConceptID=C0151699
|
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Intracranial hemorrhage</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>101799</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0151699</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Intracranial bleed; Intracranial Hemorrhages</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Intracranial hemorrhage (1386000)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0002170">HP:0002170</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Hemorrhage occurring within the skull. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet Ccolor round" title="Clinical test"><a target="_blank" href="/gtr/tests/?term=C0151699[DISCUI]&test_type=Clinical" ref="ncbi_uid=101799">C</a></span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet Vcolor" title="ClinVar"><a target="_blank" href="/clinvar?LinkName=medgen_clinvar&from_uid=101799" ref="ncbi_uid=101799">V</a></span></span><span class="TLline">Intracranial hemorrhage</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/2848" ref="tree=MeSH" title="MedGen record for Disorder of cardiovascular system">Disorder of cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/116727" ref="tree=MeSH" title="MedGen record for Abnormality of the cardiovascular system">Abnormality of the cardiovascular system</a></span><ul><li><span class="TLline"><a href="/medgen/892473" ref="tree=MeSH" title="MedGen record for Abnormal cardiovascular system morphology">Abnormal cardiovascular system morphology</a></span><ul><li><span class="TLline"><a href="/medgen/927608" ref="tree=MeSH" title="MedGen record for Abnormal vascular morphology">Abnormal vascular morphology</a></span><ul><li><span class="TLline"><a href="/medgen/867613" ref="tree=MeSH" title="MedGen record for Abnormal cerebral vascular morphology">Abnormal cerebral vascular morphology</a></span><ul><li><span class="matched_ds">Intracranial hemorrhage</span><ul><li><span class="TLline"><a href="/medgen/488779" ref="tree=MeSH" title="MedGen record for Cerebellar hemorrhage">Cerebellar hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/423648" ref="tree=MeSH" title="MedGen record for Cerebral hemorrhage">Cerebral hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/332401" ref="tree=MeSH" title="MedGen record for Antenatal intracerebral hemorrhage">Antenatal intracerebral hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/96872" ref="tree=MeSH" title="MedGen record for Basal ganglia hemorrhage">Basal ganglia hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/155623" ref="tree=MeSH" title="MedGen record for Hemorrhage in putamen">Hemorrhage in putamen</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/859286" ref="tree=MeSH" title="MedGen record for Cerebral Hemorrhage Related to Birth">Cerebral Hemorrhage Related to Birth</a></span></li><li><span class="TLline"><a href="/medgen/1371930" ref="tree=MeSH" title="MedGen record for Cerebral Intraventricular Hemorrhage">Cerebral Intraventricular Hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/858296" ref="tree=MeSH" title="MedGen record for Intraparenchymal Hemorrhage of the Newborn">Intraparenchymal Hemorrhage of the Newborn</a></span></li><li><span class="TLline"><a href="/medgen/116096" ref="tree=MeSH" title="MedGen record for Intraventricular hemorrhage">Intraventricular hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/542590" ref="tree=MeSH" title="MedGen record for Perinatal intraventricular hemorrhage">Perinatal intraventricular hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/904936" ref="tree=MeSH" title="MedGen record for Preterm intraventricular hemorrhage">Preterm intraventricular hemorrhage</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/856233" ref="tree=MeSH" title="MedGen record for Periventricular Hemorrhage of the Newborn">Periventricular Hemorrhage of the Newborn</a></span></li><li><span class="TLline"><a href="/medgen/870807" ref="tree=MeSH" title="MedGen record for Recurrent cerebral hemorrhage">Recurrent cerebral hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/473434" ref="tree=MeSH" title="MedGen record for Subependymal Hemorrhage">Subependymal Hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/634954" ref="tree=MeSH" title="MedGen record for Grade I preterm intraventricular hemorrhage">Grade I preterm intraventricular hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/634956" ref="tree=MeSH" title="MedGen record for Perinatal subependymal hemorrhage with intraventricular and intracerebral extension">Perinatal subependymal hemorrhage with intraventricular and intracerebral extension</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/66764" ref="tree=MeSH" title="MedGen record for Epidural hemorrhage">Epidural hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/232928" ref="tree=MeSH" title="MedGen record for Nontraumatic extradural hemorrhage">Nontraumatic extradural hemorrhage</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/155952" ref="tree=MeSH" title="MedGen record for Intracranial Hemorrhage, Hypertensive">Intracranial Hemorrhage, Hypertensive</a></span></li><li><span class="TLline"><a href="/medgen/163141" ref="tree=MeSH" title="MedGen record for Intracranial Tumor Hemorrhage">Intracranial Tumor Hemorrhage</a></span></li><li><span class="TLline"><a href="/medgen/473180" ref="tree=MeSH" title="MedGen record for Perinatal intracranial hemorrhage">Perinatal intracranial hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/858300" ref="tree=MeSH" title="MedGen record for Intracranial Hemorrhage Related to Birth">Intracranial Hemorrhage Related to Birth</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/18489" ref="tree=MeSH" title="MedGen record for Pituitary apoplexy">Pituitary apoplexy</a></span></li><li><span class="TLline"><a href="/medgen/11625" ref="tree=MeSH" title="MedGen record for Subarachnoid hemorrhage">Subarachnoid hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/856649" ref="tree=MeSH" title="MedGen record for Subarachnoid Hemorrhage Related to Birth">Subarachnoid Hemorrhage Related to Birth</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/6775" ref="tree=MeSH" title="MedGen record for Subdural hemorrhage">Subdural hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/155446" ref="tree=MeSH" title="MedGen record for Hematoma, Subdural, Acute">Hematoma, Subdural, Acute</a></span></li><li><span class="TLline"><a href="/medgen/155445" ref="tree=MeSH" title="MedGen record for Hematoma, Subdural, Chronic">Hematoma, Subdural, Chronic</a></span></li><li><span class="TLline"><a href="/medgen/155517" ref="tree=MeSH" title="MedGen record for Spinal subdural hematoma">Spinal subdural hematoma</a></span></li><li><span class="TLline"><a href="/medgen/857042" ref="tree=MeSH" title="MedGen record for Subdural Hemorrhage Related to Birth">Subdural Hemorrhage Related to Birth</a></span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Conditions_with_this_feature">Conditions with this feature</h1><a sid="112" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_44030"><div><strong>Menkes kinky-hair syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>44030</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0022716</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Menkes disease (MNK) is an X-linked recessive disorder characterized by generalized copper deficiency. The clinical features result from the dysfunction of several copper-dependent enzymes.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/44030">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_52736"><div><strong>Glanzmann thrombasthenia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>52736</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0040015</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Glanzmann thrombasthenia is a bleeding disorder that is characterized by prolonged or spontaneous bleeding starting from birth. People with Glanzmann thrombasthenia tend to bruise easily, have frequent nosebleeds (epistaxis), and may bleed from the gums. They may also develop red or purple spots on the skin caused by bleeding underneath the skin (petechiae) or swelling caused by bleeding within tissues (hematoma). Glanzmann thrombasthenia can also cause prolonged bleeding following injury, trauma, or surgery (including dental work). Women with this condition can have prolonged and sometimes abnormally heavy menstrual bleeding. Affected women also have an increased risk of excessive blood loss during pregnancy and childbirth.\n\nAbout a quarter of individuals with Glanzmann thrombasthenia have bleeding in the gastrointestinal tract, which often occurs later in life. Rarely, affected individuals have bleeding inside the skull (intracranial hemorrhage) or joints (hemarthrosis).\n\nThe severity and frequency of the bleeding episodes in Glanzmann thrombasthenia can vary greatly among affected individuals, even in the same family. Spontaneous bleeding tends to become less frequent with age.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/52736">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75677"><div><strong>Infantile hypophosphatasia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75677</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0268412</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Hypophosphatasia is characterized by defective mineralization of growing or remodeling bone, with or without root-intact tooth loss, in the presence of low activity of serum and bone alkaline phosphatase. Clinical features range from stillbirth without mineralized bone at the severe end to pathologic fractures of the lower extremities in later adulthood at the mild end. While the disease spectrum is a continuum, seven clinical forms of hypophosphatasia are usually recognized based on age at diagnosis and severity of features: Perinatal (severe): Characterized by pulmonary insufficiency and hypercalcemia Perinatal (benign): Prenatal skeletal manifestations that slowly resolve into one of the milder forms Infantile: Onset between birth and age six months of clinical features of rickets without elevated serum alkaline phosphatase activity Severe childhood (juvenile): Variable presenting features progressing to rickets Mild childhood: Low bone mineral density for age, increased risk of fracture, and premature loss of primary teeth with intact roots Adult: Characterized by stress fractures and pseudofractures of the lower extremities in middle age, sometimes associated with early loss of adult dentition Odontohypophosphatasia: Characterized by premature exfoliation of primary teeth and/or severe dental caries without skeletal manifestations</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75677">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_473015"><div><strong>Congenital factor VII deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>473015</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0272320</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare, genetic, congenital vitamin K-dependant coagulation factor deficiency disorder characterized by decreased levels or absence of coagulation factor VII (FVII), resulting in bleeding diathesis of variable severity.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/473015">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_543976"><div><strong>Hereditary factor X deficiency disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>543976</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C0272327</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/543976">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_279656"><div><strong>Hereditary cerebral amyloid angiopathy, Icelandic type</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>279656</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1527338</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cerebral amyloid angiopathy (CAA), defined by the deposition of congophilic material in the vessels of the cortex and leptomeninges, is a major cause of intracerebral hemorrhage in the elderly (Vinters, 1987, Greenberg, 1998). Palsdottir et al. (1988) referred to the disorder in Icelandic patients as hereditary cystatin C amyloid angiopathy (HCCAA).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/279656">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_347062"><div><strong>Circumvallate placenta syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347062</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1859089</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347062">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_354864"><div><strong>Aneurysm, intracranial berry type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>354864</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C1862932</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Rupture of an intracranial aneurysm, an outpouching or sac-like widening of a cerebral artery, leads to a subarachnoid hemorrhage, a sudden-onset disease that can lead to severe disability and death. Several risk factors such as smoking, hypertension, and excessive alcohol intake are associated with subarachnoid hemorrhage (summary by Krischek and Inoue, 2006). Genetic Heterogeneity of Intracranial Berry Aneurysm Intracranial berry aneurysm-1 (ANIB1) has been mapped to chromosome 7q11.2. Other mapped loci for intracranial berry aneurysm include ANIB2 (608542) on chromosome 19q13, ANIB3 (609122) on 1p36.13-p34.3, ANIB4 (610213) on 5p15.2-14.3, ANIB5 (300870) on Xp22, ANIB6 (611892) on 9p21, ANIB7 (612161) on 11q24-q25, ANIB8 (612162) on 14q23, ANIB9 (612586) on 2q, ANIB10 (612587) on 8q, and ANIB11 (614252) on 8p22. ANIB12 (618734) is caused by mutation in the THSD1 gene (616821).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/354864">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_442497"><div><strong>Factor XIII, A subunit, deficiency of</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>442497</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2750514</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Factor XIII deficiency is an autosomal recessive hematologic disorder characterized by increased bleeding and poor wound healing. Most cases of congenital factor XIII deficiency result from mutation in the A subunit (Kangsadalampai et al., 1999). Ichinose et al. (1996, 2000) proposed a classification of factor XIII deficiency: XIIIA deficiency (formerly 'type II' F13 deficiency) and XIIIB deficiency (formerly 'type I' F13 deficiency), as well as a possible combined deficiency of the 2.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/442497">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_418825"><div><strong>Cerebral cavernous malformation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>418825</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C2919945</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Congenital Abnormality</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Familial cerebral cavernous malformations (FCCM) is a disorder characterized by multiple vascular lesions in the brain and spinal cord that consist of clustered, endothelial-lined caverns ranging in diameter from a few millimeters to several centimeters. Cerebral and/or spinal cavernous malformations may increase in number over time, and individual lesions may increase or decrease in size. The number of cerebral cavernous malformations (CCMs) identified in an individual ranges from one or two to hundreds of lesions (typical number 6-20 CCMs) depending on the individual's age and the quality and type of brain imaging used. Although CCMs have been reported in infants and children, the majority become evident between the second and fifth decades of life either incidentally or associated with seizures, focal neurologic deficits, headaches, and/or cerebral hemorrhage. Cutaneous vascular lesions are found in 9% and retinal vascular lesions in almost 5% of affected individuals. Up to 50% of individuals with FCCM remain symptom free throughout their lives.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/418825">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_482396"><div><strong>Joubert syndrome 14</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>482396</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3280766</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Classic Joubert syndrome (JS) is characterized by three primary findings: A distinctive cerebellar and brain stem malformation called the molar tooth sign (MTS). Hypotonia. Developmental delays. Often these findings are accompanied by episodic tachypnea or apnea and/or atypical eye movements. In general, the breathing abnormalities improve with age, truncal ataxia develops over time, and acquisition of gross motor milestones is delayed. Cognitive abilities are variable, ranging from severe intellectual disability to normal. Additional findings can include retinal dystrophy, renal disease, ocular colobomas, occipital encephalocele, hepatic fibrosis, polydactyly, oral hamartomas, and endocrine abnormalities. Both intra- and interfamilial variation are seen.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/482396">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_482600"><div><strong>Porencephaly 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>482600</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C3280970</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Brain small vessel disease-2 is an autosomal dominant disorder characterized by variable neurologic impairment resulting from disturbed vascular supply that leads to cerebral degeneration. The disorder is often associated with 'porencephaly' on brain imaging. Affected individuals typically have hemiplegia, seizures, and intellectual disability, although the severity is variable (summary by Yoneda et al., 2012). For a discussion of genetic heterogeneity of brain small vessel disease, see BSVD1 (175780).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/482600">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_924576"><div><strong>MIRAGE syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>924576</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4284088</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">MIRAGE syndrome is an acronym for the major findings of myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy. Cytopenias are typically seen soon after birth; thrombocytopenia is the most common followed by anemia and pancytopenia. Recurrent infections from early infancy include pneumonia, urinary tract infection, gastroenteritis, meningitis, otitis media, dermatitis, subcutaneous abscess, and sepsis. Reported genital phenotypes in those with 46,XY karyotype included hypospadias, microphallus, bifid shawl scrotum, ambiguous genitalia, or complete female genitalia. Hypoplastic or dysgenetic ovaries have been reported in females. Gastrointestinal complications include chronic diarrhea and esophageal dysfunction. Moderate-to-severe developmental delay is reported in most affected individuals. Autonomic dysfunction and renal dysfunction are also reported.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/924576">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934771"><div><strong>SIN3A-related intellectual disability syndrome due to a point mutation</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934771</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C4310804</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Witteveen-Kolk syndrome (WITKOS) is an autosomal dominant disorder with characteristic distinctive facial features, microcephaly, short stature, and mildly impaired intellectual development with delayed cognitive and motor development and subtle anomalies on MRI-brain imaging (summary by Balasubramanian et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934771">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1841145"><div><strong>Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1841145</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information.">C5830509</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity (NEDIHSS) is an autosomal recessive disorder characterized by prenatal or neonatal onset of intracranial hemorrhage, usually with ventriculomegaly and calcifications, resulting in parenchymal brain damage. Some affected individuals have symptoms incompatible with life and die in utero. Those that survive show profound global developmental delay with almost no motor or cognitive skills, hypotonia, spasticity, and seizures. Other features may include facial dysmorphism, retinal vascular abnormalities, and poor overall growth. The pathogenesis of the disease likely results from dysfunction of vascular endothelial cells in the brain (Lecca et al., 2023).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1841145">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_354864" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Aneurysm, intracranial berry type 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_418825" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebral cavernous malformation</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347062" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Circumvallate placenta syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_473015" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital factor VII deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_442497" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Factor XIII, A subunit, deficiency of</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (15)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_52736" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Glanzmann thrombasthenia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_279656" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary cerebral amyloid angiopathy, Icelandic type</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_543976" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary factor X deficiency disease</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75677" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Infantile hypophosphatasia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_482396" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Joubert syndrome 14</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_44030" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Menkes kinky-hair syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_924576" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">MIRAGE syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1841145" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_482600" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Porencephaly 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934771" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">SIN3A-related intellectual disability syndrome due to a point mutation</a></div></span></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_105">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
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||
<div class="nl"><a target="_blank" href="/pubmed/34989711">Executive Summary of Recommendations and Expert Consensus for Plasma and Platelet Transfusion Practice in Critically Ill Children: From the Transfusion and Anemia EXpertise Initiative-Control/Avoidance of Bleeding (TAXI-CAB).</a></div>
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||
<div class="portlet_content ln"><span class="medgenPMauthor">Nellis ME,
|
||
Karam O,
|
||
Valentine SL,
|
||
Bateman ST,
|
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Remy KE,
|
||
Lacroix J,
|
||
Cholette JM,
|
||
Bembea MM,
|
||
Russell RT,
|
||
Steiner ME,
|
||
Goobie SM,
|
||
Tucci M,
|
||
Stricker PA,
|
||
Stanworth SJ,
|
||
Delaney M,
|
||
Lieberman L,
|
||
Muszynski JA,
|
||
Bauer DF,
|
||
Steffen K,
|
||
Nishijima D,
|
||
Ibla J,
|
||
Emani S,
|
||
Vogel AM,
|
||
Haas T,
|
||
Goel R,
|
||
Crighton G,
|
||
Delgado D,
|
||
Demetres M,
|
||
Parker RI;
|
||
Pediatric Critical Care Transfusion and Anemia EXpertise Initiative—Control/Avoidance of Bleeding (TAXI-CAB), in collaboration with the Pediatric Critical Care Blood Research Network (BloodNet), and the Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network</span><br />
|
||
<span class="medgenPMjournal">Pediatr Crit Care Med</span>
|
||
2022 Jan 1;23(1):34-51.
|
||
doi: 10.1097/PCC.0000000000002851.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34989711" target="_blank">34989711</a><a href="/pmc/articles/PMC8820267" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26426232">Management of Intracranial Pressure.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Freeman WD</span><br />
|
||
<span class="medgenPMjournal">Continuum (Minneap Minn)</span>
|
||
2015 Oct;21(5 Neurocritical Care):1299-323.
|
||
doi: 10.1212/CON.0000000000000235.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26426232" target="_blank">26426232</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25383671">Platelet transfusion: a clinical practice guideline from the AABB.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kaufman RM,
|
||
Djulbegovic B,
|
||
Gernsheimer T,
|
||
Kleinman S,
|
||
Tinmouth AT,
|
||
Capocelli KE,
|
||
Cipolle MD,
|
||
Cohn CS,
|
||
Fung MK,
|
||
Grossman BJ,
|
||
Mintz PD,
|
||
O'Malley BA,
|
||
Sesok-Pizzini DA,
|
||
Shander A,
|
||
Stack GE,
|
||
Webert KE,
|
||
Weinstein R,
|
||
Welch BG,
|
||
Whitman GJ,
|
||
Wong EC,
|
||
Tobian AA;
|
||
AABB</span><br />
|
||
<span class="medgenPMjournal">Ann Intern Med</span>
|
||
2015 Feb 3;162(3):205-13.
|
||
doi: 10.7326/M14-1589.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25383671" target="_blank">25383671</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22intracranial%20hemorrhage%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (937)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29869130">Therapeutic Approach to Hypertensive Emergencies: Hemorrhagic Stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Salvetti M,
|
||
Paini A,
|
||
Bertacchini F,
|
||
Aggiusti C,
|
||
Stassaldi D,
|
||
Verzeri L,
|
||
Saccà G,
|
||
Muiesan ML</span><br />
|
||
<span class="medgenPMjournal">High Blood Press Cardiovasc Prev</span>
|
||
2018 Jun;25(2):191-195.
|
||
Epub 2018 Jun 4
|
||
doi: 10.1007/s40292-018-0262-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29869130" target="_blank">29869130</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28959487">Current management of spontaneous intracerebral haemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dastur CK,
|
||
Yu W</span><br />
|
||
<span class="medgenPMjournal">Stroke Vasc Neurol</span>
|
||
2017 Mar;2(1):21-29.
|
||
Epub 2017 Feb 24
|
||
doi: 10.1136/svn-2016-000047.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28959487" target="_blank">28959487</a><a href="/pmc/articles/PMC5435209" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22167847">Intracranial hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Naidech AM</span><br />
|
||
<span class="medgenPMjournal">Am J Respir Crit Care Med</span>
|
||
2011 Nov 1;184(9):998-1006.
|
||
doi: 10.1164/rccm.201103-0475CI.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22167847" target="_blank">22167847</a><a href="/pmc/articles/PMC3361326" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17992038">Ossified cephalhematoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta PK,
|
||
Mathew GS,
|
||
Malik AK,
|
||
Al Derazi T</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neurosurg</span>
|
||
2007;43(6):492-7.
|
||
doi: 10.1159/000108793.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17992038" target="_blank">17992038</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16710967">Surgical management of acute epidural hematomas.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bullock MR,
|
||
Chesnut R,
|
||
Ghajar J,
|
||
Gordon D,
|
||
Hartl R,
|
||
Newell DW,
|
||
Servadei F,
|
||
Walters BC,
|
||
Wilberger JE;
|
||
Surgical Management of Traumatic Brain Injury Author Group</span><br />
|
||
<span class="medgenPMjournal">Neurosurgery</span>
|
||
2006 Mar;58(3 Suppl):S7-15; discussion Si-iv.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16710967" target="_blank">16710967</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intracranial%20hemorrhage%22%20AND%20Etiology%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (7925)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38575257">Headache due to Vascular Disorders.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rothrock JF</span><br />
|
||
<span class="medgenPMjournal">Neurol Clin</span>
|
||
2024 May;42(2):375-388.
|
||
Epub 2024 Feb 13
|
||
doi: 10.1016/j.ncl.2023.12.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38575257" target="_blank">38575257</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29869130">Therapeutic Approach to Hypertensive Emergencies: Hemorrhagic Stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Salvetti M,
|
||
Paini A,
|
||
Bertacchini F,
|
||
Aggiusti C,
|
||
Stassaldi D,
|
||
Verzeri L,
|
||
Saccà G,
|
||
Muiesan ML</span><br />
|
||
<span class="medgenPMjournal">High Blood Press Cardiovasc Prev</span>
|
||
2018 Jun;25(2):191-195.
|
||
Epub 2018 Jun 4
|
||
doi: 10.1007/s40292-018-0262-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29869130" target="_blank">29869130</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22167847">Intracranial hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Naidech AM</span><br />
|
||
<span class="medgenPMjournal">Am J Respir Crit Care Med</span>
|
||
2011 Nov 1;184(9):998-1006.
|
||
doi: 10.1164/rccm.201103-0475CI.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22167847" target="_blank">22167847</a><a href="/pmc/articles/PMC3361326" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17992038">Ossified cephalhematoma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gupta PK,
|
||
Mathew GS,
|
||
Malik AK,
|
||
Al Derazi T</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neurosurg</span>
|
||
2007;43(6):492-7.
|
||
doi: 10.1159/000108793.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17992038" target="_blank">17992038</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17073042">Shaken baby syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Miehl NJ</span><br />
|
||
<span class="medgenPMjournal">J Forensic Nurs</span>
|
||
2005 Fall;1(3):111-7.
|
||
doi: 10.1111/j.1939-3938.2005.tb00027.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17073042" target="_blank">17073042</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intracranial%20hemorrhage%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4470)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37277200">Mechanical Thrombectomy for Large Ischemic Stroke: A Systematic Review and Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li Q,
|
||
Abdalkader M,
|
||
Siegler JE,
|
||
Yaghi S,
|
||
Sarraj A,
|
||
Campbell BCV,
|
||
Yoo AJ,
|
||
Zaidat OO,
|
||
Kaesmacher J,
|
||
Pujara D,
|
||
Nogueira RG,
|
||
Saver JL,
|
||
Li L,
|
||
Han Q,
|
||
Dai Y,
|
||
Sang H,
|
||
Yang Q,
|
||
Nguyen TN,
|
||
Qiu Z</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2023 Aug 29;101(9):e922-e932.
|
||
Epub 2023 Jun 5
|
||
doi: 10.1212/WNL.0000000000207536.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37277200" target="_blank">37277200</a><a href="/pmc/articles/PMC10501098" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36315950">Comparative Effectiveness and Safety Between Apixaban, Dabigatran, Edoxaban, and Rivaroxaban Among Patients With Atrial Fibrillation : A Multinational Population-Based Cohort Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lau WCY,
|
||
Torre CO,
|
||
Man KKC,
|
||
Stewart HM,
|
||
Seager S,
|
||
Van Zandt M,
|
||
Reich C,
|
||
Li J,
|
||
Brewster J,
|
||
Lip GYH,
|
||
Hingorani AD,
|
||
Wei L,
|
||
Wong ICK</span><br />
|
||
<span class="medgenPMjournal">Ann Intern Med</span>
|
||
2022 Nov;175(11):1515-1524.
|
||
Epub 2022 Nov 1
|
||
doi: 10.7326/M22-0511.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36315950" target="_blank">36315950</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34010530">Endovascular Therapy for Stroke Due to Basilar-Artery Occlusion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Langezaal LCM,
|
||
van der Hoeven EJRJ,
|
||
Mont'Alverne FJA,
|
||
de Carvalho JJF,
|
||
Lima FO,
|
||
Dippel DWJ,
|
||
van der Lugt A,
|
||
Lo RTH,
|
||
Boiten J,
|
||
Lycklama À Nijeholt GJ,
|
||
Staals J,
|
||
van Zwam WH,
|
||
Nederkoorn PJ,
|
||
Majoie CBLM,
|
||
Gerber JC,
|
||
Mazighi M,
|
||
Piotin M,
|
||
Zini A,
|
||
Vallone S,
|
||
Hofmeijer J,
|
||
Martins SO,
|
||
Nolte CH,
|
||
Szabo K,
|
||
Dias FA,
|
||
Abud DG,
|
||
Wermer MJH,
|
||
Remmers MJM,
|
||
Schneider H,
|
||
Rueckert CM,
|
||
de Laat KF,
|
||
Yoo AJ,
|
||
van Doormaal PJ,
|
||
van Es ACGM,
|
||
Emmer BJ,
|
||
Michel P,
|
||
Puetz V,
|
||
Audebert HJ,
|
||
Pontes-Neto OM,
|
||
Vos JA,
|
||
Kappelle LJ,
|
||
Algra A,
|
||
Schonewille WJ;
|
||
BASICS Study Group</span><br />
|
||
<span class="medgenPMjournal">N Engl J Med</span>
|
||
2021 May 20;384(20):1910-1920.
|
||
doi: 10.1056/NEJMoa2030297.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34010530" target="_blank">34010530</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33045929">Tenecteplase Thrombolysis for Acute Ischemic Stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Warach SJ,
|
||
Dula AN,
|
||
Milling TJ Jr</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2020 Nov;51(11):3440-3451.
|
||
Epub 2020 Oct 13
|
||
doi: 10.1161/STROKEAHA.120.029749.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33045929" target="_blank">33045929</a><a href="/pmc/articles/PMC7606819" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31738483">A Comparison of Two LDL Cholesterol Targets after Ischemic Stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Amarenco P,
|
||
Kim JS,
|
||
Labreuche J,
|
||
Charles H,
|
||
Abtan J,
|
||
Béjot Y,
|
||
Cabrejo L,
|
||
Cha JK,
|
||
Ducrocq G,
|
||
Giroud M,
|
||
Guidoux C,
|
||
Hobeanu C,
|
||
Kim YJ,
|
||
Lapergue B,
|
||
Lavallée PC,
|
||
Lee BC,
|
||
Lee KB,
|
||
Leys D,
|
||
Mahagne MH,
|
||
Meseguer E,
|
||
Nighoghossian N,
|
||
Pico F,
|
||
Samson Y,
|
||
Sibon I,
|
||
Steg PG,
|
||
Sung SM,
|
||
Touboul PJ,
|
||
Touzé E,
|
||
Varenne O,
|
||
Vicaut É,
|
||
Yelles N,
|
||
Bruckert E;
|
||
Treat Stroke to Target Investigators</span><br />
|
||
<span class="medgenPMjournal">N Engl J Med</span>
|
||
2020 Jan 2;382(1):9.
|
||
Epub 2019 Nov 18
|
||
doi: 10.1056/NEJMoa1910355.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31738483" target="_blank">31738483</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intracranial%20hemorrhage%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (5943)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31370070">The Role of Abnormal Hemostasis and Fibrinolysis in Morbidity and Mortality of Acute Promyelocytic Leukemia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kwaan HC,
|
||
Weiss I,
|
||
Tallman MS</span><br />
|
||
<span class="medgenPMjournal">Semin Thromb Hemost</span>
|
||
2019 Sep;45(6):612-621.
|
||
Epub 2019 Aug 1
|
||
doi: 10.1055/s-0039-1693478.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31370070" target="_blank">31370070</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31230137">Maternal Stroke: an Update.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zambrano MD,
|
||
Miller EC</span><br />
|
||
<span class="medgenPMjournal">Curr Atheroscler Rep</span>
|
||
2019 Jun 22;21(9):33.
|
||
doi: 10.1007/s11883-019-0798-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31230137" target="_blank">31230137</a><a href="/pmc/articles/PMC6815220" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28987431">Spontaneous Intracerebral Hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Alerhand S,
|
||
Lay C</span><br />
|
||
<span class="medgenPMjournal">Emerg Med Clin North Am</span>
|
||
2017 Nov;35(4):825-845.
|
||
doi: 10.1016/j.emc.2017.07.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28987431" target="_blank">28987431</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9260508">Hypertensive intracranial hemorrhage.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Brewington KC 2nd,
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<div class="nl"><a target="_blank" href="/pubmed/3397796">Intracranial hemorrhage in newborn and young infants with hemophilia.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Yoffe G,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intracranial%20hemorrhage%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4067)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/37296161">The accuracy of non-contrast brain CT scan in predicting the presence of a vascular etiology in patients with primary intracranial hemorrhage.</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/36762852">Trial of Endovascular Therapy for Acute Ischemic Stroke with Large Infarct.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Huo X,
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Ma G,
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Tong X,
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Zhang X,
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Pan Y,
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Nguyen TN,
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Yuan G,
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Han H,
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Chen W,
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Wei M,
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Zhang J,
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Zhou Z,
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Yao X,
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Wang G,
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Song W,
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Cai X,
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Nan G,
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Li D,
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Ling W,
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Cai C,
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Wen C,
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Wang E,
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Zhang L,
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Jiang C,
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Liu Y,
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Liao G,
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Chen X,
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Li T,
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Liu S,
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Li J,
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Gao F,
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Ma N,
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Mo D,
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Song L,
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Sun X,
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Li X,
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Deng Y,
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Luo G,
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Lv M,
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He H,
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Liu A,
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Zhang J,
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Mu S,
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Liu L,
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Jing J,
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Nie X,
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Ding Z,
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Du W,
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Zhao X,
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Yang P,
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Liu L,
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Wang Y,
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Liebeskind DS,
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Pereira VM,
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Ren Z,
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Wang Y,
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Miao Z;
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ANGEL-ASPECT Investigators</span><br />
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<span class="medgenPMjournal">N Engl J Med</span>
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2023 Apr 6;388(14):1272-1283.
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Epub 2023 Feb 10
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doi: 10.1056/NEJMoa2213379.
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<span class="bold">PMID: </span><a href="/pubmed/36762852" target="_blank">36762852</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/31009346">S100B Serum Elevation Predicts In-Hospital Mortality After Brain Arteriovenous Malformation Rupture.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Shotar E,
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Amouyal C,
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Jacquens A,
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Mathon B,
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Monneret D,
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Premat K,
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Lenck S,
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Sourour NA,
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Clarençon F,
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Degos V</span><br />
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<span class="medgenPMjournal">Stroke</span>
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2019 May;50(5):1250-1253.
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doi: 10.1161/STROKEAHA.119.025033.
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||
<span class="bold">PMID: </span><a href="/pubmed/31009346" target="_blank">31009346</a></div>
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||
<div class="nl"><a target="_blank" href="/pubmed/28590352">Big for small: Validating brain injury guidelines in pediatric traumatic brain injury.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Azim A,
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Jehan FS,
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Rhee P,
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O'Keeffe T,
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Tang A,
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Vercruysse G,
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Kulvatunyou N,
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<span class="medgenPMjournal">J Trauma Acute Care Surg</span>
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2017 Dec;83(6):1200-1204.
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doi: 10.1097/TA.0000000000001611.
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<span class="bold">PMID: </span><a href="/pubmed/28590352" target="_blank">28590352</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/16710967">Surgical management of acute epidural hematomas.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Bullock MR,
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Chesnut R,
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Ghajar J,
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Gordon D,
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Hartl R,
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Newell DW,
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Servadei F,
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Walters BC,
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Surgical Management of Traumatic Brain Injury Author Group</span><br />
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<span class="medgenPMjournal">Neurosurgery</span>
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2006 Mar;58(3 Suppl):S7-15; discussion Si-iv.
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<span class="bold">PMID: </span><a href="/pubmed/16710967" target="_blank">16710967</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intracranial%20hemorrhage%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (4938)</a></div></div>
|
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|
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|
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<div class="portlet mgSection" id="ID_104">
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/36951049">Complications of Intravenous Tenecteplase Versus Alteplase for the Treatment of Acute Ischemic Stroke: A Systematic Review and Meta-Analysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Rose D,
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Cavalier A,
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Kam W,
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Cantrell S,
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Lusk J,
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Schrag M,
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Yaghi S,
|
||
Stretz C,
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||
de Havenon A,
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||
Saldanha IJ,
|
||
Wu TY,
|
||
Ranta A,
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||
Barber PA,
|
||
Marriott E,
|
||
Feng W,
|
||
Kosinski AS,
|
||
Laskowitz D,
|
||
Poli S,
|
||
Mac Grory B</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2023 May;54(5):1192-1204.
|
||
Epub 2023 Mar 23
|
||
doi: 10.1161/STROKEAHA.122.042335.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36951049" target="_blank">36951049</a><a href="/pmc/articles/PMC10133185" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36331504">Evaluation of Direct Oral Anticoagulant Reversal Agents in Intracranial Hemorrhage: A Systematic Review and Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chaudhary R,
|
||
Singh A,
|
||
Chaudhary R,
|
||
Bashline M,
|
||
Houghton DE,
|
||
Rabinstein A,
|
||
Adamski J,
|
||
Arndt R,
|
||
Ou NN,
|
||
Rudis MI,
|
||
Brown CS,
|
||
Wieruszewski ED,
|
||
Wanek M,
|
||
Brinkman NJ,
|
||
Linderbaum JA,
|
||
Sorenson MA,
|
||
Atkinson JL,
|
||
Thompson KM,
|
||
Aiyer AN,
|
||
McBane RD 2nd</span><br />
|
||
<span class="medgenPMjournal">JAMA Netw Open</span>
|
||
2022 Nov 1;5(11):e2240145.
|
||
doi: 10.1001/jamanetworkopen.2022.40145.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36331504" target="_blank">36331504</a><a href="/pmc/articles/PMC9636520" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33272127">Intravenous Thrombolysis With Tenecteplase in Patients With Large Vessel Occlusions: Systematic Review and Meta-Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Katsanos AH,
|
||
Safouris A,
|
||
Sarraj A,
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||
Magoufis G,
|
||
Leker RR,
|
||
Khatri P,
|
||
Cordonnier C,
|
||
Leys D,
|
||
Shoamanesh A,
|
||
Ahmed N,
|
||
Alexandrov AV,
|
||
Tsivgoulis G</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2021 Jan;52(1):308-312.
|
||
Epub 2020 Dec 4
|
||
doi: 10.1161/STROKEAHA.120.030220.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33272127" target="_blank">33272127</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31200607">Risk factors for intracranial hemorrhage after mechanical thrombectomy: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hao Z,
|
||
Yang C,
|
||
Xiang L,
|
||
Wu B,
|
||
Liu M</span><br />
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<span class="medgenPMjournal">Expert Rev Neurother</span>
|
||
2019 Oct;19(10):927-935.
|
||
Epub 2019 Jul 5
|
||
doi: 10.1080/14737175.2019.1632191.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31200607" target="_blank">31200607</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28720644">Effects of Non-Vitamin K Antagonist Oral Anticoagulants Versus Warfarin in Patients With Atrial Fibrillation and Valvular Heart Disease: A Systematic Review and Meta-Analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pan KL,
|
||
Singer DE,
|
||
Ovbiagele B,
|
||
Wu YL,
|
||
Ahmed MA,
|
||
Lee M</span><br />
|
||
<span class="medgenPMjournal">J Am Heart Assoc</span>
|
||
2017 Jul 18;6(7)
|
||
doi: 10.1161/JAHA.117.005835.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28720644" target="_blank">28720644</a><a href="/pmc/articles/PMC5586302" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Intracranial%20hemorrhage%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (662)</a></div></div>
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