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<!--
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||
UID=6775
|
||
ConceptID=C0018946
|
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Subdural hemorrhage</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>6775</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.">C0018946</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Hematoma, Subdural; Hematomas, Subdural; Hemorrhage, Subdural; Hemorrhages, Subdural; Subdural Hematoma; Subdural Hematomas; Subdural Hemorrhage; Subdural Hemorrhages</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>SDH - Subdural hematoma (95453001); Subdural hematoma (95453001); Subdural intracranial hemorrhage (35486000); Subdural intracranial hematoma (95453001); Subdural hemorrhage (35486000)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0100309">HP:0100309</a></td></tr>
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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>
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||
<div class="portlet_content ln">Hemorrhage occurring between the dura mater and the arachnoid mater. [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 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>
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<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 unavailable round" title="Clinical test">C</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 unavailable" title="ClinVar">V</span></span><span class="TLline">Subdural hemorrhage</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/19974" ref="tree=MeSH" title="MedGen record for Clinical finding">Clinical finding</a></span><ul><li><span class="TLline"><a href="/medgen/232191" ref="tree=MeSH" title="MedGen record for Finding by Cause">Finding by Cause</a></span><ul><li><span class="TLline"><a href="/medgen/5503" ref="tree=MeSH" title="MedGen record for Hemorrhage">Hemorrhage</a></span><ul><li><span class="TLline"><a href="/medgen/5484" ref="tree=MeSH" title="MedGen record for Hematoma">Hematoma</a></span><ul><li><span class="matched_ds">Subdural hemorrhage</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></div></div></div></div>
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<div class="portlet mgSection" id="ID_112">
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<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>
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<div class="portlet_content ln clinfeat">
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||
<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_124337"><div><strong>Glutaric aciduria, type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>124337</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.">C0268595</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The phenotypic spectrum of untreated glutaric acidemia type 1 (GA-1) ranges from the more common form (infantile-onset disease) to the less common form (later-onset disease – i.e., after age 6 years). Of note, the GA-1 phenotype can vary widely between untreated family members with the same genotype, primarily as a function of the age at which the first acute encephalopathic crisis occurred: three months to six years in infantile-onset GA-1 and after age six years in later-onset GA-1. Characteristically these crises result in acute bilateral striatal injury and subsequent complex movement disorders. In the era of newborn screening (NBS), the prompt initiation of treatment of asymptomatic infants detected by NBS means that most individuals who would have developed manifestations of either infantile-onset or later-onset GA-1 remain asymptomatic; however, they may be at increased risk for other manifestations (e.g., renal disease) that are becoming apparent as the understanding of the natural history of treated GA-1 continues to evolve.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/124337">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_333324"><div><strong>TARP syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>333324</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.">C1839463</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The classic features of TARP syndrome are talipes equinovarus, atrial septal defect, Robin sequence (micrognathia, cleft palate, and glossoptosis), and persistent left superior vena cava. Not all patients have all classic features. Some patients have the additional features of central nervous system dysfunction, renal abnormalities, variable cardiac anomalies including hypertrophic obstructive cardiomyopathy, and variable distal limb defects including syndactyly. Most patients die in late prenatal or early postnatal stages (summary by Kaeppler et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/333324">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_749036"><div><strong>Congenital afibrinogenemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>749036</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.">C2584774</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Inherited disorders of fibrinogen affect either the quantity (afibrinogenemia and hypofibrinogenemia; 202400) or the quality (dysfibrinogenemia; 616004) of the circulating fibrinogen or both (hypodysfibrinogenemia; see 616004). Afibrinogenemia is characterized by the complete absence of immunoreactive fibrinogen. Bleeding due to afibrinogenemia usually manifests in the neonatal period, with 85% of cases presenting umbilical cord bleeding, but a later age of onst is not unusual. Bleeding may occur in the skin, gastrointestinal tract, genitourinary tract, or the central nervous system, with intracranial hemorrhage being reported as the major cause of death. Patients are susceptible to spontaneous rupture of the spleen. Menstruating women may experience menometrorrhagia. First-trimester abortion is common. Both arterial and venous thromboembolic complications have been reported (summary by de Moerloose and Neerman-Arbez, 2009). Hypofibrinogenemia is characterized by reduced amounts of immunoreactive fibrinogen. Patients are often heterozygous carriers of afibrinogenemia mutations and are usually asymptomatic. However, they may bleed when exposed to trauma or if they have a second associated hemostatic abnormality. Women may experience miscarriages. Liver disease occurs in rare cases (summary by de Moerloose and Neerman-Arbez, 2009).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/749036">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1631944"><div><strong>Fetal akinesia-cerebral and retinal hemorrhage syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1631944</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.">C4706410</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Lethal congenital contracture syndrome-5 (LCCS5) is an autosomal recessive disorder characterized by decreased fetal movements, joint contractures, hypotonia, skeletal abnormalities with thin bones, and brain and retinal hemorrhages (Koutsopoulos et al., 2013). For a general phenotypic description and a discussion of genetic heterogeneity of LCCS, see LCCS1 (253310).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1631944">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1648362"><div><strong>Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1648362</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.">C4749003</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">SMALED2B is a severe neuromuscular disorder with onset in utero. Affected individuals show decreased fetal movements and are usually born with congenital contractures consistent with arthrogryposis multiplex congenita (AMC). After birth, they have severe hypotonia and muscle atrophy as well as respiratory insufficiency due to muscle weakness. Some patients may have dysmorphic facial features and/or abnormalities on brain imaging. Many patients die in early childhood (summary by Storbeck et al., 2017) For discussion of genetic heterogeneity of lower extremity-predominant spinal muscular atrophy, see SMALED1 (158600).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1648362">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794278"><div><strong>Congenital disorder of glycosylation, type Iw, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794278</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.">C5562068</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Autosomal dominant congenital disorder of glycosylation type Iw (CDG1WAD) is characterized by variable skeletal anomalies, short stature, macrocephaly, and dysmorphic features; about half of patients have impaired intellectual development. Additional features include increased muscle tone and muscle cramps (Wilson et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794278">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1840969"><div><strong>Congenital myopathy 2c, severe infantile, autosomal dominant</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840969</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.">C5830333</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Congenital myopathy-2C (CMYO2C) is an autosomal dominant disorder of the skeletal muscle characterized by severe congenital weakness usually resulting in death from respiratory failure in the first year or so of life. Patients present at birth with hypotonia, lack of antigravity movements, poor head control, and difficulties feeding or breathing, often requiring tube-feeding and mechanical ventilation. Decreased fetal movements may be observed in some cases. Of the patients with congenital myopathy caused by mutation in the ACTA1 gene, about 90% carry heterozygous mutations that are usually de novo and cause the severe infantile phenotype. Some patients with heterozygous mutations have a more typical and milder disease course with delayed motor development and proximal muscle weakness, but are able to achieve independent ambulation (CMYO2A; 161800). The severity of the disease most likely depends on the detrimental effect of the mutation, although there are probably additional modifying factors (Ryan et al., 2001; Laing et al., 2009; Sanoudou and Beggs, 2001; Agrawal et al., 2004; Nowak et al., 2013; Sewry et al., 2019; Laitila and Wallgren-Pettersson, 2021). For a discussion of genetic heterogeneity of congenital myopathy, see CMYO1A (117000).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1840969">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1854940"><div><strong>Intellectual developmental disorder, x-linked, syndromic 37</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1854940</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.">C5935567</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">X-linked syndromic intellectual developmental disorder-37 (MRXS37) is a developmental disorder showing phenotypic variability and variable severity. Male mutation carriers tend to be more severely affected than female mutation carriers, some of whom may even be asymptomatic. In general, the disorder is characterized by global developmental delay with delayed walking, speech delay, impaired intellectual development that ranges from borderline low to moderate, and behavioral abnormalities, such as autism and sleeping difficulties. Many patients are able to attend mainstream schools with assistance and work under supervision. Additional more variable features include sensorineural hearing loss, ocular anomalies, feeding difficulties, dysmorphic facial features, inguinal and umbilical hernia, genitourinary defects, congenital heart defects, musculoskeletal anomalies, and endocrine dysfunction, such as hypogonadism or hyperparathyroidism (Shepherdson et al., 2024).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1854940">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_749036" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital afibrinogenemia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794278" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital disorder of glycosylation, type Iw, autosomal dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1840969" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Congenital myopathy 2c, severe infantile, autosomal dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1631944" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Fetal akinesia-cerebral and retinal hemorrhage syndrome</a></div>
|
||
<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="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (9)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_124337" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Glutaric aciduria, type 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1854940" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual developmental disorder, x-linked, syndromic 37</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1648362" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_333324" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">TARP syndrome</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>
|
||
<div class="nl"><a target="_blank" href="/pubmed/31675688">Abusive head trauma: evidence, obfuscation, and informed management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duhaime AC,
|
||
Christian CW</span><br />
|
||
<span class="medgenPMjournal">J Neurosurg Pediatr</span>
|
||
2019 Nov 1;24(5):481-488.
|
||
doi: 10.3171/2019.7.PEDS18394.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31675688" target="_blank">31675688</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30223973">Management of Intracranial Hemorrhage in the Anticoagulated Patient.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Macdonald RL</span><br />
|
||
<span class="medgenPMjournal">Neurosurg Clin N Am</span>
|
||
2018 Oct;29(4):605-613.
|
||
Epub 2018 Aug 14
|
||
doi: 10.1016/j.nec.2018.06.013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30223973" target="_blank">30223973</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29796797">Consensus statement on abusive head trauma in infants and young children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Choudhary AK,
|
||
Servaes S,
|
||
Slovis TL,
|
||
Palusci VJ,
|
||
Hedlund GL,
|
||
Narang SK,
|
||
Moreno JA,
|
||
Dias MS,
|
||
Christian CW,
|
||
Nelson MD Jr,
|
||
Silvera VM,
|
||
Palasis S,
|
||
Raissaki M,
|
||
Rossi A,
|
||
Offiah AC</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2018 Aug;48(8):1048-1065.
|
||
Epub 2018 May 23
|
||
doi: 10.1007/s00247-018-4149-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29796797" target="_blank">29796797</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22subdural%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 (34)</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/39102615">Timing of Anticoagulation Resumption and Risk of Ischemic and Hemorrhagic Complications in Patients With ICH and Mechanical Heart Valves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sakusic A,
|
||
Rabinstein AA,
|
||
Anisetti B,
|
||
Mandrekar J,
|
||
Wijdicks EFM,
|
||
Freeman WD,
|
||
Braksick SA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2024 Aug 27;103(4):e209664.
|
||
Epub 2024 Aug 5
|
||
doi: 10.1212/WNL.0000000000209664.
|
||
<span class="bold">PMID: </span><a href="/pubmed/39102615" target="_blank">39102615</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37806180">Implications of intracranial hemorrhage associated with stereo-EEG.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agashe S,
|
||
Brinkmann BH,
|
||
Cox BC,
|
||
Wong-Kisiel L,
|
||
Van Gompel JJ,
|
||
Marsh RW,
|
||
Miller KJ,
|
||
Krecke KN,
|
||
Britton JW</span><br />
|
||
<span class="medgenPMjournal">Clin Neurophysiol</span>
|
||
2023 Nov;155:86-93.
|
||
Epub 2023 Sep 6
|
||
doi: 10.1016/j.clinph.2023.08.016.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37806180" target="_blank">37806180</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36261511">Current issues and controversies surrounding spine imaging and the significance of spinal subdural hemorrhage in suspected abusive head trauma.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Canty KW,
|
||
Feldman KW,
|
||
Bartnik-Olson B,
|
||
Choudhary AK,
|
||
Shiroishi MS;
|
||
ENIGMA Child Abuse Working Group</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2022 Dec;52(13):2445-2449.
|
||
Epub 2022 Oct 20
|
||
doi: 10.1007/s00247-022-05534-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36261511" target="_blank">36261511</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35188950">Risk Factors and Prognosis of Early Posttraumatic Seizures in Moderate to Severe Traumatic Brain Injury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Laing J,
|
||
Gabbe B,
|
||
Chen Z,
|
||
Perucca P,
|
||
Kwan P,
|
||
O'Brien TJ</span><br />
|
||
<span class="medgenPMjournal">JAMA Neurol</span>
|
||
2022 Apr 1;79(4):334-341.
|
||
doi: 10.1001/jamaneurol.2021.5420.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35188950" target="_blank">35188950</a><a href="/pmc/articles/PMC8861899" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8594217">Posttraumatic cerebral arterial spasm.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Martin NA,
|
||
Doberstein C,
|
||
Alexander M,
|
||
Khanna R,
|
||
Benalcazar H,
|
||
Alsina G,
|
||
Zane C,
|
||
McBride D,
|
||
Kelly D,
|
||
Hovda D</span><br />
|
||
<span class="medgenPMjournal">J Neurotrauma</span>
|
||
1995 Oct;12(5):897-901.
|
||
doi: 10.1089/neu.1995.12.897.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8594217" target="_blank">8594217</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subdural%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 (381)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29796797">Consensus statement on abusive head trauma in infants and young children.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Choudhary AK,
|
||
Servaes S,
|
||
Slovis TL,
|
||
Palusci VJ,
|
||
Hedlund GL,
|
||
Narang SK,
|
||
Moreno JA,
|
||
Dias MS,
|
||
Christian CW,
|
||
Nelson MD Jr,
|
||
Silvera VM,
|
||
Palasis S,
|
||
Raissaki M,
|
||
Rossi A,
|
||
Offiah AC</span><br />
|
||
<span class="medgenPMjournal">Pediatr Radiol</span>
|
||
2018 Aug;48(8):1048-1065.
|
||
Epub 2018 May 23
|
||
doi: 10.1007/s00247-018-4149-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29796797" target="_blank">29796797</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29555403">Spinal Cord Hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shaban A,
|
||
Moritani T,
|
||
Al Kasab S,
|
||
Sheharyar A,
|
||
Limaye KS,
|
||
Adams HP Jr</span><br />
|
||
<span class="medgenPMjournal">J Stroke Cerebrovasc Dis</span>
|
||
2018 Jun;27(6):1435-1446.
|
||
Epub 2018 Mar 16
|
||
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<div class="nl"><a target="_blank" href="/pubmed/39102615">Timing of Anticoagulation Resumption and Risk of Ischemic and Hemorrhagic Complications in Patients With ICH and Mechanical Heart Valves.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/25782563">Cupping (Hijama) Treatment: Benign or Sinister?</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/37806180">Implications of intracranial hemorrhage associated with stereo-EEG.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/35188950">Risk Factors and Prognosis of Early Posttraumatic Seizures in Moderate to Severe Traumatic Brain Injury.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Laing J,
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Perucca P,
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Kwan P,
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<div class="nl"><a target="_blank" href="/pubmed/29555403">Spinal Cord Hemorrhage.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Shaban A,
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Moritani T,
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Al Kasab S,
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Sheharyar A,
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Limaye KS,
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doi: 10.1016/j.jstrokecerebrovasdis.2018.02.014.
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<span class="bold">PMID: </span><a href="/pubmed/29555403" target="_blank">29555403</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28877540">Evidence for the Use of Tranexamic Acid in Subarachnoid and Subdural Hemorrhage: A Systematic Review.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Anker-Møller T,
|
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Troldborg A,
|
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Sunde N,
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Hvas AM</span><br />
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<span class="medgenPMjournal">Semin Thromb Hemost</span>
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2017 Oct;43(7):750-758.
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Epub 2017 Sep 6
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doi: 10.1055/s-0037-1604089.
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<span class="bold">PMID: </span><a href="/pubmed/28877540" target="_blank">28877540</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25616019">Shaken Baby Syndrome: a review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mian M,
|
||
Shah J,
|
||
Dalpiaz A,
|
||
Schwamb R,
|
||
Miao Y,
|
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Warren K,
|
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Khan S</span><br />
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<span class="medgenPMjournal">Fetal Pediatr Pathol</span>
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2015 Jun;34(3):169-75.
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Epub 2015 Jan 23
|
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doi: 10.3109/15513815.2014.999394.
|
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<span class="bold">PMID: </span><a href="/pubmed/25616019" target="_blank">25616019</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subdural%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 (230)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/39102615">Timing of Anticoagulation Resumption and Risk of Ischemic and Hemorrhagic Complications in Patients With ICH and Mechanical Heart Valves.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sakusic A,
|
||
Rabinstein AA,
|
||
Anisetti B,
|
||
Mandrekar J,
|
||
Wijdicks EFM,
|
||
Freeman WD,
|
||
Braksick SA</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2024 Aug 27;103(4):e209664.
|
||
Epub 2024 Aug 5
|
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doi: 10.1212/WNL.0000000000209664.
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||
<span class="bold">PMID: </span><a href="/pubmed/39102615" target="_blank">39102615</a></div>
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||
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||
<div class="nl"><a target="_blank" href="/pubmed/38472247">Imaging predictors of hemorrhagic progression of a contusion after traumatic brain injury: a systematic review and meta-analysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Peng J,
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Luo T,
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Li X,
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Li B,
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Cheng Y,
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<span class="bold">PMID: </span><a href="/pubmed/38472247" target="_blank">38472247</a><a href="/pmc/articles/PMC10933276" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div class="nl"><a target="_blank" href="/pubmed/38457956">Venous sinus stenting for idiopathic intracranial hypertension: An updated Meta-analysis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Azzam AY,
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Mortezaei A,
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Morsy MM,
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Essibayi MA,
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Ghozy S,
|
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Elamin O,
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Azab MA,
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Elswedy A,
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Altschul D,
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Kadirvel R,
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Brinjikji W,
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Kallmes DF</span><br />
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<span class="medgenPMjournal">J Neurol Sci</span>
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2024 Apr 15;459:122948.
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Epub 2024 Mar 5
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doi: 10.1016/j.jns.2024.122948.
|
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<span class="bold">PMID: </span><a href="/pubmed/38457956" target="_blank">38457956</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35188950">Risk Factors and Prognosis of Early Posttraumatic Seizures in Moderate to Severe Traumatic Brain Injury.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Laing J,
|
||
Gabbe B,
|
||
Chen Z,
|
||
Perucca P,
|
||
Kwan P,
|
||
O'Brien TJ</span><br />
|
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<span class="medgenPMjournal">JAMA Neurol</span>
|
||
2022 Apr 1;79(4):334-341.
|
||
doi: 10.1001/jamaneurol.2021.5420.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35188950" target="_blank">35188950</a><a href="/pmc/articles/PMC8861899" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17618985">Traumatic brain injury in infants: the phenomenon of subdural hemorrhage with hemispheric hypodensity ("Big Black Brain").</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Duhaime AC,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subdural%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 (213)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<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>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/38457956">Venous sinus stenting for idiopathic intracranial hypertension: An updated Meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Azzam AY,
|
||
Mortezaei A,
|
||
Morsy MM,
|
||
Essibayi MA,
|
||
Ghozy S,
|
||
Elamin O,
|
||
Azab MA,
|
||
Elswedy A,
|
||
Altschul D,
|
||
Kadirvel R,
|
||
Brinjikji W,
|
||
Kallmes DF</span><br />
|
||
<span class="medgenPMjournal">J Neurol Sci</span>
|
||
2024 Apr 15;459:122948.
|
||
Epub 2024 Mar 5
|
||
doi: 10.1016/j.jns.2024.122948.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38457956" target="_blank">38457956</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33693899">Sport-Related Structural Brain Injury and Return to Play: Systematic Review and Expert Insight.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Zuckerman SL,
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Yengo-Kahn AM,
|
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Tang AR,
|
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Bailes JE,
|
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Beauchamp K,
|
||
Berger MS,
|
||
Bonfield CM,
|
||
Camarata PJ,
|
||
Cantu RC,
|
||
Davis GA,
|
||
Ellenbogen RG,
|
||
Ellis MJ,
|
||
Feuer H,
|
||
Guazzo E,
|
||
Harris OA,
|
||
Heppner P,
|
||
Honeybul S,
|
||
Manley G,
|
||
Maroon JC,
|
||
Miele VJ,
|
||
Nahed BV,
|
||
Okonkwo DO,
|
||
Oppenlander ME,
|
||
Petty J,
|
||
Sabin HI,
|
||
Samadani U,
|
||
Sherburn EW,
|
||
Sheridan M,
|
||
Tator CH,
|
||
Theodore N,
|
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Timmons SD,
|
||
Woodworth GF,
|
||
Solomon GS,
|
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Sills AK</span><br />
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<span class="medgenPMjournal">Neurosurgery</span>
|
||
2021 May 13;88(6):E495-E504.
|
||
doi: 10.1093/neuros/nyab041.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33693899" target="_blank">33693899</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30481628">Middle Meningeal Artery Embolization for Chronic Subdural Hematoma: Meta-Analysis and Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Srivatsan A,
|
||
Mohanty A,
|
||
Nascimento FA,
|
||
Hafeez MU,
|
||
Srinivasan VM,
|
||
Thomas A,
|
||
Chen SR,
|
||
Johnson JN,
|
||
Kan P</span><br />
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<span class="medgenPMjournal">World Neurosurg</span>
|
||
2019 Feb;122:613-619.
|
||
Epub 2018 Nov 24
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||
doi: 10.1016/j.wneu.2018.11.167.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30481628" target="_blank">30481628</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29476390">Spontaneous Intracranial Hemorrhage in Pregnancy: A Systematic Review of the Literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ascanio LC,
|
||
Maragkos GA,
|
||
Young BC,
|
||
Boone MD,
|
||
Kasper EM</span><br />
|
||
<span class="medgenPMjournal">Neurocrit Care</span>
|
||
2019 Feb;30(1):5-15.
|
||
doi: 10.1007/s12028-018-0501-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29476390" target="_blank">29476390</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28877540">Evidence for the Use of Tranexamic Acid in Subarachnoid and Subdural Hemorrhage: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Anker-Møller T,
|
||
Troldborg A,
|
||
Sunde N,
|
||
Hvas AM</span><br />
|
||
<span class="medgenPMjournal">Semin Thromb Hemost</span>
|
||
2017 Oct;43(7):750-758.
|
||
Epub 2017 Sep 6
|
||
doi: 10.1055/s-0037-1604089.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28877540" target="_blank">28877540</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Subdural%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 (16)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
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|
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|
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</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
||
|
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<!-- MedGen supplemental column starts here -->
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<div class="portlet mgSection" id="ID_113">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Subdural%20hemorrhage" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
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</div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22subdural%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">PubMed</a><div class="help-popup">See practice and clinical guidelines in PubMed. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li><li><a target="_blank" href="/books/?term=((%22clinical%20guidelines%22%5BResource%20Type%5D)%20OR%20%22practice%20guideline%22%5BPublication%20Type%5D)%20AND%20(%22Subdural%20hemorrhage%22)">Bookshelf</a><div class="help-popup">See practice and clinical guidelines in NCBI Bookshelf. The search results may include broader topics and may not capture all published guidelines. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div></li></ul></div>
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