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<!--
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UID=488779
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ConceptID=C0149854
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Cerebellar hemorrhage</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>488779</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.">C0149854</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Pathologic Function</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Cerebellar haemorrhage; Hemorrhagic cerebellum</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Cerebellar hemorrhage (75038005); Hemorrhagic cerebellum (75038005)</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:0011695">HP:0011695</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>
|
||
<div class="portlet_content ln">Hemorrhage into the parenchyma of the cerebellum. [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>
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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">Cerebellar hemorrhage</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><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="TLline"><a href="/medgen/101799" ref="tree=MeSH" title="MedGen record for Intracranial hemorrhage">Intracranial hemorrhage</a></span><ul><li><span class="matched_ds">Cerebellar hemorrhage</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
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</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_82822"><div><strong>Isovaleryl-CoA dehydrogenase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>82822</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.">C0268575</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Individuals with clinical manifestations of isovaleric acidemia (IVA) have either classic IVA identified on newborn screening or classic IVA with a later diagnosis due to a missed diagnosis or later onset of clinical manifestations. Classic IVA is characterized by acute metabolic decompensations (vomiting, poor feeding, lethargy, hypotonia, seizures, and a distinct odor of sweaty feet). Acute metabolic decompensations are typically triggered by fasting, (febrile) illness (especially gastroenteritis), or increased protein intake. Clinical deterioration often occurs within hours to days after birth. Additional manifestations of classic IVA include developmental delay, intellectual disability and/or impaired cognition, epilepsy, and movement disorder (tremor, dysmetria, extrapyramidal movements). Early treatment in those identified by newborn screening can significantly reduce morbidity and mortality in individuals with classic IVA.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/82822">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_75694"><div><strong>Propionic acidemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>75694</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.">C0268579</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The spectrum of propionic acidemia (PA) ranges from neonatal onset to late-onset disease. Neonatal-onset PA, the most common form, is characterized by a healthy newborn with poor feeding and decreased arousal in the first few days of life, followed by progressive encephalopathy of unexplained origin. Without prompt diagnosis (often through newborn screening) and management, this is followed by progressive encephalopathy manifesting as lethargy, seizures, or coma that can result in death. It is frequently accompanied by metabolic acidosis with anion gap, lactic acidosis, ketonuria, hypoglycemia, hyperammonemia, and cytopenias. Individuals with late-onset PA may remain asymptomatic and suffer a metabolic crisis under catabolic stress (e.g., illness, surgery, fasting) or may experience a more insidious onset with the development of multiorgan complications including vomiting, protein intolerance, failure to thrive, hypotonia, developmental delays or regression, movement disorders, or cardiomyopathy. Isolated cardiomyopathy can be observed on rare occasions in the absence of clinical metabolic decompensation or neurocognitive deficits. Manifestations of neonatal-onset and late-onset PA over time can include growth impairment, intellectual disability, seizures, basal ganglia lesions, pancreatitis, cardiomyopathy, and chronic kidney disease. Other rarely reported complications include optic atrophy, sensorineural hearing loss, and premature ovarian insufficiency.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/75694">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_344424"><div><strong>Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>344424</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.">C1855114</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">For this GeneReview, the term "isolated methylmalonic acidemia" refers to a group of inborn errors of metabolism associated with elevated methylmalonic acid (MMA) concentration in the blood and urine that result from the failure to isomerize (convert) methylmalonyl-coenzyme A (CoA) into succinyl-CoA during propionyl-CoA metabolism in the mitochondrial matrix, without hyperhomocysteinemia or homocystinuria, hypomethioninemia, or variations in other metabolites, such as malonic acid. Isolated MMA is caused by complete or partial deficiency of the enzyme methylmalonyl-CoA mutase (mut0 enzymatic subtype or mut– enzymatic subtype, respectively), a defect in the transport or synthesis of its cofactor, 5-deoxy-adenosyl-cobalamin (cblA, cblB, or cblD-MMA), or deficiency of the enzyme methylmalonyl-CoA epimerase. Prior to the advent of newborn screening, common phenotypes included: Infantile/non-B12-responsive form (mut0 enzymatic subtype, cblB), the most common phenotype, associated with infantile-onset lethargy, tachypnea, hypothermia, vomiting, and dehydration on initiation of protein-containing feeds. Without appropriate treatment, the infantile/non-B12-responsive phenotype could rapidly progress to coma due to hyperammonemic encephalopathy. Partially deficient or B12-responsive phenotypes (mut– enzymatic subtype, cblA, cblB [rare], cblD-MMA), in which symptoms occur in the first few months or years of life and are characterized by feeding problems, failure to thrive, hypotonia, and developmental delay marked by episodes of metabolic decompensation. Methylmalonyl-CoA epimerase deficiency, in which findings range from complete absence of symptoms to severe metabolic acidosis. Affected individuals can also develop ataxia, dysarthria, hypotonia, mild spastic paraparesis, and seizures. In those individuals diagnosed by newborn screening and treated from an early age, there appears to be decreased early mortality, less severe symptoms at diagnosis, favorable short-term neurodevelopmental outcome, and lower incidence of movement disorders and irreversible cerebral damage. However, secondary complications may still occur and can include intellectual disability, tubulointerstitial nephritis with progressive impairment of renal function, "metabolic stroke" (bilateral lacunar infarction of the basal ganglia during acute metabolic decompensation), pancreatitis, growth failure, functional immune impairment, bone marrow failure, optic nerve atrophy, arrhythmias and/or cardiomyopathy (dilated or hypertrophic), liver steatosis/fibrosis/cancer, and renal cancer.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/344424">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_414044"><div><strong>Cerebral amyloid angiopathy, APP-related</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>414044</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.">C2751536</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Two types of hereditary cerebral amyloid angiopathy, known as familial British dementia and familial Danish dementia, are characterized by dementia and movement problems. Strokes are uncommon in these types. People with the Danish type also have clouding of the lens of the eyes (cataracts) and deafness.\n\nStrokes are rare in people with the Arctic type of hereditary cerebral amyloid angiopathy, in which the first sign is usually memory loss that then progresses to severe dementia. Strokes are also uncommon in individuals with the Iowa type. This type is characterized by memory loss, problems with vocabulary and the production of speech, personality changes, and involuntary muscle twitches (myoclonus).\n\nThe first sign of the Icelandic type of hereditary cerebral amyloid angiopathy is typically a stroke followed by dementia. Strokes associated with the Icelandic type usually occur earlier than the other types, with individuals typically experiencing their first stroke in their twenties or thirties.\n\nPeople with the Flemish and Italian types of hereditary cerebral amyloid angiopathy are prone to recurrent strokes and dementia. Individuals with the Piedmont type may have one or more strokes and typically experience impaired movements, numbness or tingling (paresthesias), confusion, or dementia.\n\nThe Dutch type of hereditary cerebral amyloid angiopathy is the most common form. Stroke is frequently the first sign of the Dutch type and is fatal in about one third of people who have this condition. Survivors often develop dementia and have recurrent strokes. About half of individuals with the Dutch type who have one or more strokes will have recurrent seizures (epilepsy).\n\nThere are many different types of hereditary cerebral amyloid angiopathy. The different types are distinguished by their genetic cause, which determines whether areas of the brain other than blood vessels are affected, and the signs and symptoms that occur. The various types of hereditary cerebral amyloid angiopathy are named after the regions where they were first diagnosed.\n\nHereditary cerebral amyloid angiopathy is a condition characterized by an abnormal buildup of protein clumps called amyloid deposits in the blood vessels in the brain, causing vascular disease (angiopathy). People with hereditary cerebral amyloid angiopathy often have progressive loss of intellectual function (dementia), stroke, and other neurological problems starting in mid-adulthood. Due to neurological decline, this condition is typically fatal in one's sixties, although there is variation depending on the severity of the signs and symptoms. Most affected individuals die within a decade after signs and symptoms first appear, although some people with the disease have survived longer.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/414044">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_414044" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cerebral amyloid angiopathy, APP-related</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_82822" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Isovaleryl-CoA dehydrogenase deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_344424" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_75694" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Propionic acidemia</a></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/34799840">Prenatal Diagnosis and Neurodevelopmental Outcome in Isolated Cerebellar Hypoplasia of Suspected Hemorrhagic Etiology: a Retrospective Cohort Study.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scelsa B,
|
||
Cutillo G,
|
||
Lanna MM,
|
||
Righini A,
|
||
Balestriero MA,
|
||
Brazzoduro V,
|
||
Zambrano S,
|
||
Parazzini C,
|
||
Alfei E,
|
||
Rustico M</span><br />
|
||
<span class="medgenPMjournal">Cerebellum</span>
|
||
2022 Dec;21(6):944-953.
|
||
Epub 2021 Nov 20
|
||
doi: 10.1007/s12311-021-01341-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34799840" target="_blank">34799840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4546748">Cerebellar hemorrhage: diagnosis and treatment. A review of 56 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ott KH,
|
||
Kase CS,
|
||
Ojemann RG,
|
||
Mohr JP</span><br />
|
||
<span class="medgenPMjournal">Arch Neurol</span>
|
||
1974 Sep;31(3):160-7.
|
||
doi: 10.1001/archneur.1974.00490390042003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4546748" target="_blank">4546748</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14260181">ACUTE HYPERTENSIVE CEREBELLAR HEMORRHAGE: DIAGNOSIS AND SURGICAL TREATMENT.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">FISHER CM,
|
||
PICARD EH,
|
||
POLAK A,
|
||
DALAL P,
|
||
POJEMANN RG</span><br />
|
||
<span class="medgenPMjournal">J Nerv Ment Dis</span>
|
||
1965 Jan;140:38-57.
|
||
doi: 10.1097/00005053-196501000-00004.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14260181" target="_blank">14260181</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22cerebellar%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 (14)</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/33272397">Hemorrhagic stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Montaño A,
|
||
Hanley DF,
|
||
Hemphill JC 3rd</span><br />
|
||
<span class="medgenPMjournal">Handb Clin Neurol</span>
|
||
2021;176:229-248.
|
||
doi: 10.1016/B978-0-444-64034-5.00019-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33272397" target="_blank">33272397</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32623579">Comparison of Long-Term Outcomes of Endoscopic and Minimally Invasive Catheter Evacuation for the Treatment of Spontaneous Cerebellar Hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Li L,
|
||
Liu H,
|
||
Luo J,
|
||
Tan Z,
|
||
Gao J,
|
||
Wang P,
|
||
Jing W,
|
||
Fan R,
|
||
Zhang X,
|
||
Guo H,
|
||
Bai H,
|
||
Cui W,
|
||
Wu X,
|
||
Qu Y,
|
||
Guo W</span><br />
|
||
<span class="medgenPMjournal">Transl Stroke Res</span>
|
||
2021 Feb;12(1):57-64.
|
||
Epub 2020 Jul 4
|
||
doi: 10.1007/s12975-020-00827-8.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32623579" target="_blank">32623579</a><a href="/pmc/articles/PMC7803713" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32800815">Randomized Controlled Early versus Late Ventricular Intervention Study in Posthemorrhagic Ventricular Dilatation: Outcome at 2 Years.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cizmeci MN,
|
||
Groenendaal F,
|
||
Liem KD,
|
||
van Haastert IC,
|
||
Benavente-Fernández I,
|
||
van Straaten HLM,
|
||
Steggerda S,
|
||
Smit BJ,
|
||
Whitelaw A,
|
||
Woerdeman P,
|
||
Heep A,
|
||
de Vries LS;
|
||
ELVIS study group</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2020 Nov;226:28-35.e3.
|
||
Epub 2020 Aug 12
|
||
doi: 10.1016/j.jpeds.2020.08.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32800815" target="_blank">32800815</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26377547">Intracranial complications associated with spinal surgery.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pham MH,
|
||
Tuchman A,
|
||
Platt A,
|
||
Hsieh PC</span><br />
|
||
<span class="medgenPMjournal">Eur Spine J</span>
|
||
2016 Mar;25(3):888-94.
|
||
Epub 2015 Sep 16
|
||
doi: 10.1007/s00586-015-4241-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26377547" target="_blank">26377547</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4546748">Cerebellar hemorrhage: diagnosis and treatment. A review of 56 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ott KH,
|
||
Kase CS,
|
||
Ojemann RG,
|
||
Mohr JP</span><br />
|
||
<span class="medgenPMjournal">Arch Neurol</span>
|
||
1974 Sep;31(3):160-7.
|
||
doi: 10.1001/archneur.1974.00490390042003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4546748" target="_blank">4546748</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%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 (206)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/32800815">Randomized Controlled Early versus Late Ventricular Intervention Study in Posthemorrhagic Ventricular Dilatation: Outcome at 2 Years.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cizmeci MN,
|
||
Groenendaal F,
|
||
Liem KD,
|
||
van Haastert IC,
|
||
Benavente-Fernández I,
|
||
van Straaten HLM,
|
||
Steggerda S,
|
||
Smit BJ,
|
||
Whitelaw A,
|
||
Woerdeman P,
|
||
Heep A,
|
||
de Vries LS;
|
||
ELVIS study group</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2020 Nov;226:28-35.e3.
|
||
Epub 2020 Aug 12
|
||
doi: 10.1016/j.jpeds.2020.08.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32800815" target="_blank">32800815</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25439293">Cerebellar hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Datar S,
|
||
Rabinstein AA</span><br />
|
||
<span class="medgenPMjournal">Neurol Clin</span>
|
||
2014 Nov;32(4):993-1007.
|
||
Epub 2014 Sep 11
|
||
doi: 10.1016/j.ncl.2014.07.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25439293" target="_blank">25439293</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3336840">Cerebellar hemorrhage: diagnosis and treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">van der Hoop RG,
|
||
Vermeulen M,
|
||
van Gijn J</span><br />
|
||
<span class="medgenPMjournal">Surg Neurol</span>
|
||
1988 Jan;29(1):6-10.
|
||
doi: 10.1016/0090-3019(88)90115-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3336840" target="_blank">3336840</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/7039001">Cerebellar hemorrhage and infarction.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Heros RC</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
1982 Jan-Feb;13(1):106-9.
|
||
doi: 10.1161/01.str.13.1.106.
|
||
<span class="bold">PMID: </span><a href="/pubmed/7039001" target="_blank">7039001</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/4546748">Cerebellar hemorrhage: diagnosis and treatment. A review of 56 cases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ott KH,
|
||
Kase CS,
|
||
Ojemann RG,
|
||
Mohr JP</span><br />
|
||
<span class="medgenPMjournal">Arch Neurol</span>
|
||
1974 Sep;31(3):160-7.
|
||
doi: 10.1001/archneur.1974.00490390042003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/4546748" target="_blank">4546748</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%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 (236)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37309686">Carotid-Cavernous Fistula: A Rare Cause of Cerebellar Hemorrhage.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Asad SD,
|
||
Nigam M,
|
||
Rhee JY,
|
||
Regenhardt RW,
|
||
Vranic JE,
|
||
Rabinov JD,
|
||
Camargo Faye E,
|
||
Silverman SB</span><br />
|
||
<span class="medgenPMjournal">Stroke</span>
|
||
2023 Aug;54(8):e407-e411.
|
||
Epub 2023 Jun 13
|
||
doi: 10.1161/STROKEAHA.122.040816.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37309686" target="_blank">37309686</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33272397">Hemorrhagic stroke.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Montaño A,
|
||
Hanley DF,
|
||
Hemphill JC 3rd</span><br />
|
||
<span class="medgenPMjournal">Handb Clin Neurol</span>
|
||
2021;176:229-248.
|
||
doi: 10.1016/B978-0-444-64034-5.00019-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33272397" target="_blank">33272397</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32800815">Randomized Controlled Early versus Late Ventricular Intervention Study in Posthemorrhagic Ventricular Dilatation: Outcome at 2 Years.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Cizmeci MN,
|
||
Groenendaal F,
|
||
Liem KD,
|
||
van Haastert IC,
|
||
Benavente-Fernández I,
|
||
van Straaten HLM,
|
||
Steggerda S,
|
||
Smit BJ,
|
||
Whitelaw A,
|
||
Woerdeman P,
|
||
Heep A,
|
||
de Vries LS;
|
||
ELVIS study group</span><br />
|
||
<span class="medgenPMjournal">J Pediatr</span>
|
||
2020 Nov;226:28-35.e3.
|
||
Epub 2020 Aug 12
|
||
doi: 10.1016/j.jpeds.2020.08.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32800815" target="_blank">32800815</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30121019">Weston-Hurst syndrome with acute hemorrhagic cerebellitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bonduelle T,
|
||
Stricker J,
|
||
Minéo JF,
|
||
Massri A,
|
||
Guesdon C,
|
||
Barroso B,
|
||
Bonnan M</span><br />
|
||
<span class="medgenPMjournal">Clin Neurol Neurosurg</span>
|
||
2018 Oct;173:118-119.
|
||
Epub 2018 Aug 11
|
||
doi: 10.1016/j.clineuro.2018.08.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30121019" target="_blank">30121019</a></div>
|
||
|
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<div class="nl"><a target="_blank" href="/pubmed/26377547">Intracranial complications associated with spinal surgery.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Pham MH,
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<div class="nl"><a target="_blank" href="/pubmed/4546748">Cerebellar hemorrhage: diagnosis and treatment. A review of 56 cases.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32623579">Comparison of Long-Term Outcomes of Endoscopic and Minimally Invasive Catheter Evacuation for the Treatment of Spontaneous Cerebellar Hemorrhage.</a></div>
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Liu H,
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Luo J,
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Tan Z,
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Gao J,
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Jing W,
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<div class="nl"><a target="_blank" href="/pubmed/32800815">Randomized Controlled Early versus Late Ventricular Intervention Study in Posthemorrhagic Ventricular Dilatation: Outcome at 2 Years.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cizmeci MN,
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<div class="nl"><a target="_blank" href="/pubmed/24524447">Neuroimaging of white matter injury, intraventricular and cerebellar hemorrhage.</a></div>
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<span class="bold">PMID: </span><a href="/pubmed/3336840" target="_blank">3336840</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/6170017">Hypertensive cerebellar hemorrhage and cerebellar hemorrhage caused by cryptic angioma: analysis of clinical observations, CT findings and outcome.</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%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 (135)</a></div></div>
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||
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|
||
|
||
<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/38985355">Risk factors of prognosis for spontaneous cerebellar hemorrhage: a systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shu J,
|
||
Wang W,
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||
Ye R,
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||
Zhou Y,
|
||
Tong J,
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||
Li X,
|
||
Lv X,
|
||
Zhang G,
|
||
Xu F,
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||
Zhang J</span><br />
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||
<span class="medgenPMjournal">Acta Neurochir (Wien)</span>
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||
2024 Jul 10;166(1):291.
|
||
doi: 10.1007/s00701-024-06174-z.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38985355" target="_blank">38985355</a><a href="/pmc/articles/PMC11236867" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32711341">A systematic review on brain injury and altered brain development in moderate-late preterm infants.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Boswinkel V,
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||
Nijboer-Oosterveld J,
|
||
Nijholt IM,
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||
Edens MA,
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||
Mulder-de Tollenaer SM,
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||
Boomsma MF,
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||
de Vries LS,
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||
van Wezel-Meijler G</span><br />
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||
<span class="medgenPMjournal">Early Hum Dev</span>
|
||
2020 Sep;148:105094.
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||
Epub 2020 May 28
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||
doi: 10.1016/j.earlhumdev.2020.105094.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32711341" target="_blank">32711341</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30341153">Neurodevelopmental Consequences of Preterm Isolated Cerebellar Hemorrhage: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hortensius LM,
|
||
Dijkshoorn ABC,
|
||
Ecury-Goossen GM,
|
||
Steggerda SJ,
|
||
Hoebeek FE,
|
||
Benders MJNL,
|
||
Dudink J</span><br />
|
||
<span class="medgenPMjournal">Pediatrics</span>
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||
2018 Nov;142(5)
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||
Epub 2018 Oct 19
|
||
doi: 10.1542/peds.2018-0609.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30341153" target="_blank">30341153</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26846668">Remote cerebellar hemorrhage after supratentorial procedures (part 1): a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sturiale CL,
|
||
Rossetto M,
|
||
Ermani M,
|
||
Volpin F,
|
||
Baro V,
|
||
Milanese L,
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||
Denaro L,
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||
d'Avella D</span><br />
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<span class="medgenPMjournal">Neurosurg Rev</span>
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||
2016 Oct;39(4):565-73.
|
||
Epub 2016 Feb 4
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doi: 10.1007/s10143-015-0691-6.
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||
<span class="bold">PMID: </span><a href="/pubmed/26846668" target="_blank">26846668</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26627110">Remote cerebellar hemorrhage after spinal procedures (part 2): a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sturiale CL,
|
||
Rossetto M,
|
||
Ermani M,
|
||
Baro V,
|
||
Volpin F,
|
||
Milanese L,
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Denaro L,
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d'Avella D</span><br />
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2016 Jul;39(3):369-76.
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||
<span class="bold">PMID: </span><a href="/pubmed/26627110" target="_blank">26627110</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Cerebellar%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 (10)</a></div></div>
|
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<div class="supplemental col three_col last">
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=Cerebellar%20hemorrhage" target="_blank">ClinicalTrials.gov</a></li></ul></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></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=(%22cerebellar%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(%22Cerebellar%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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<a href="/pubmed?term=Cerebellar%20hemorrhage%20AND%20humans[mesh]%20AND%20review[publication%20type]" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=2&linkpostotal=2" target="_blank">Reviews in PubMed</a>
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