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<meta name="keywords" content="C4225318, disease or syndrome, epilepsy, familial temporal lobe, 8, epilepsy, familial temporal lobe, type 8, etl8, familial temporal lobe epilepsy 8, familial temporal lobe epilepsy type 8, gal, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
|
||
UID=909158
|
||
ConceptID=C4225318
|
||
-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Familial temporal lobe epilepsy 8<span class="h1sub">(ETL8)</span></div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>909158</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."><span class="highlight" style="background-color:">C4225318</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>EPILEPSY, FAMILIAL TEMPORAL LOBE, 8; ETL8</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td><a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#target-gene-loc">Gene (location):<img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a><div class="display-none" id="target-gene-loc">
|
||
Gene(s) directly associated with<br />
|
||
this condition or phenotype.</div></td>
|
||
<td><a target="_blank" title="GAL - ID: 51083 - NCBI Gene" href="/gene/51083" class="medgenPMinfo">GAL</a> (11q13.2)</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0014650" target="_blank">MONDO:0014650</a></td></tr>
|
||
<tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/616461" target="_blank">616461</a></td></tr>
|
||
</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
|
||
<div class="portlet mgSection" id="ID_100">
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||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">A temporal lobe epilepsy characterized by autosomal dominant inheritance of complex partial seizures with occasional secondary generalization and that has material basis in heterozygous mutation in the GAL gene on chromosome 11q13. [from <a title="Monarch Initiative" href="https://monarchinitiative.org/" class="defSource" target="_blank">MONDO</a>]</div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_102">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_features">Clinical features</h1><a sid="102" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln clinfeat"><strong>From HPO</strong><br />
|
||
<div class="divPopper rprt" id="clin_41442"><div><strong>Deja vu aura</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>41442</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.">C0011194</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental Process</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A subjective feeling that an experience which is occurring for the first time has been experienced before.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen?term=%22Deja%20vu%20aura%22%5BClinical%20Features%5D%20OR%2041442%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_543022"><div><strong>Focal impaired awareness seizure</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>543022</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.">C0270834</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Focal impaired awareness seizure (or focal seizure with impaired or lost awareness) is a type of focal-onset seizure characterized by some degree (which may be partial) of impairment of the person's awareness of themselves or their surroundings at any point during the seizure.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/543022">Feature record</a> | <a href="/medgen?term=%22Focal%20impaired%20awareness%20seizure%22%5BClinical%20Features%5D%20OR%20543022%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_164077"><div><strong>Bilateral tonic-clonic seizure with focal onset</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>164077</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.">C0877017</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A bilateral tonic-clonic seizure with focal onset is a focal-onset seizure which progresses into a bilateral tonic-clonic phase.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/164077">Feature record</a> | <a href="/medgen?term=%22Bilateral%20tonic-clonic%20seizure%20with%20focal%20onset%22%5BClinical%20Features%5D%20OR%20164077%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_1710223"><div><strong>Focal aware cognitive seizure with forced thinking</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1710223</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.">C5397715</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A focal cognitive seizure with forced thinking characterized by retained awareness throughout the seizure.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1710223">Feature record</a> | <a href="/medgen?term=%22Focal%20aware%20cognitive%20seizure%20with%20forced%20thinking%22%5BClinical%20Features%5D%20OR%201710223%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_1712433"><div><strong>Focal aware autonomic seizure with epigastric sensation/nausea/vomiting/other gastrointestinal phenomena</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1712433</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.">C5397795</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A focal autonomic seizure with epigastric sensation / nausea / vomiting / other gastrointestinal phenomena characterized by retained awareness throughout the seizure.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1712433">Feature record</a> | <a href="/medgen?term=%22Focal%20aware%20autonomic%20seizure%20with%20epigastric%20sensation%2Fnausea%2Fvomiting%2Fother%20gastrointestinal%20phenomena%22%5BClinical%20Features%5D%20OR%201712433%5Buid%5D">Search on this feature</a></div></div>
|
||
<div class="divPopper rprt" id="clin_1712570"><div><strong>Focal aware sensory seizure with auditory features</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1712570</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.">C5397869</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A type of focal sensory seizure with auditory features during which awareness is retained throughout the seizure.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1712570">Feature record</a> | <a href="/medgen?term=%22Focal%20aware%20sensory%20seizure%20with%20auditory%20features%22%5BClinical%20Features%5D%20OR%201712570%5Buid%5D">Search on this feature</a></div></div><div class="TreeLite"><ul><li><span class="TLline">Abnormality of the nervous system</span><ul><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_164077" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Bilateral tonic-clonic seizure with focal onset</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_41442" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Deja vu aura</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_1712433" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal aware autonomic seizure with epigastric sensation/nausea/vomiting/other gastrointestinal phenomena</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_1710223" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal aware cognitive seizure with forced thinking</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_1712570" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal aware sensory seizure with auditory features</a></span></li><li class="TLline">
|
||
<span class="TLline"><a title="click for more information" class="jig-ncbipopper" href="#clin_543022" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Focal impaired awareness seizure</a></span></li></ul></li></ul></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/22323750">Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ho YY,
|
||
Ionita-Laza I,
|
||
Ottman R</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2012 Feb 21;78(8):563-8.
|
||
Epub 2012 Feb 8
|
||
doi: 10.1212/WNL.0b013e318247ccbf.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22323750" target="_blank">22323750</a><a href="/pmc/articles/PMC3280014" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11571336">EEG criteria predictive of complicated evolution in idiopathic rolandic epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Massa R,
|
||
de Saint-Martin A,
|
||
Carcangiu R,
|
||
Rudolf G,
|
||
Seegmuller C,
|
||
Kleitz C,
|
||
Metz-Lutz MN,
|
||
Hirsch E,
|
||
Marescaux C</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2001 Sep 25;57(6):1071-9.
|
||
doi: 10.1212/wnl.57.6.1071.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11571336" target="_blank">11571336</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(familial%20temporal%20lobe%20epilepsy%208)%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 (2)</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/34171625">Female preponderance in genetic generalized epilepsies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Videira G,
|
||
Gabriel D,
|
||
Freitas J,
|
||
Samões R,
|
||
Chorão R,
|
||
Lopes J,
|
||
Ramalheira J,
|
||
Lemos C,
|
||
Leal B,
|
||
da Silva AM,
|
||
Chaves J</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2021 Oct;91:167-171.
|
||
Epub 2021 Jun 16
|
||
doi: 10.1016/j.seizure.2021.06.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34171625" target="_blank">34171625</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24315020">Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fanciulli M,
|
||
Di Bonaventura C,
|
||
Egeo G,
|
||
Fattouch J,
|
||
Dazzo E,
|
||
Radovic S,
|
||
Spadotto A,
|
||
Giallonardo AT,
|
||
Nobile C</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Res</span>
|
||
2014 Feb;108(2):232-40.
|
||
Epub 2013 Nov 18
|
||
doi: 10.1016/j.eplepsyres.2013.11.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24315020" target="_blank">24315020</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22105092">Genetics of temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hwang SK,
|
||
Hirose S</span><br />
|
||
<span class="medgenPMjournal">Brain Dev</span>
|
||
2012 Sep;34(8):609-16.
|
||
Epub 2011 Nov 21
|
||
doi: 10.1016/j.braindev.2011.10.008.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22105092" target="_blank">22105092</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16832669">Temporal lobe resections.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harkness W</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2006 Aug;22(8):936-44.
|
||
Epub 2006 Jul 11
|
||
doi: 10.1007/s00381-006-0140-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16832669" target="_blank">16832669</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9633726">Nocturnal temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bernasconi A,
|
||
Andermann F,
|
||
Cendes F,
|
||
Dubeau F,
|
||
Andermann E,
|
||
Olivier A</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
1998 Jun;50(6):1772-7.
|
||
doi: 10.1212/wnl.50.6.1772.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9633726" target="_blank">9633726</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20temporal%20lobe%20epilepsy%208%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 (63)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28681459">Familial mesial temporal lobe epilepsy and the borderland of déjà vu.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Perucca P,
|
||
Crompton DE,
|
||
Bellows ST,
|
||
McIntosh AM,
|
||
Kalincik T,
|
||
Newton MR,
|
||
Vajda FJE,
|
||
Scheffer IE,
|
||
Kwan P,
|
||
O'Brien TJ,
|
||
Tan KM,
|
||
Berkovic SF</span><br />
|
||
<span class="medgenPMjournal">Ann Neurol</span>
|
||
2017 Aug;82(2):166-176.
|
||
Epub 2017 Jul 19
|
||
doi: 10.1002/ana.24984.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28681459" target="_blank">28681459</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24315020">Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fanciulli M,
|
||
Di Bonaventura C,
|
||
Egeo G,
|
||
Fattouch J,
|
||
Dazzo E,
|
||
Radovic S,
|
||
Spadotto A,
|
||
Giallonardo AT,
|
||
Nobile C</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Res</span>
|
||
2014 Feb;108(2):232-40.
|
||
Epub 2013 Nov 18
|
||
doi: 10.1016/j.eplepsyres.2013.11.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24315020" target="_blank">24315020</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12391356">Exercise-induced temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sturm JW,
|
||
Fedi M,
|
||
Berkovic SF,
|
||
Reutens DC</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2002 Oct 22;59(8):1246-8.
|
||
doi: 10.1212/wnl.59.8.1246.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12391356" target="_blank">12391356</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9633726">Nocturnal temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bernasconi A,
|
||
Andermann F,
|
||
Cendes F,
|
||
Dubeau F,
|
||
Andermann E,
|
||
Olivier A</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
1998 Jun;50(6):1772-7.
|
||
doi: 10.1212/wnl.50.6.1772.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9633726" target="_blank">9633726</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/106817">Epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gilligan B</span><br />
|
||
<span class="medgenPMjournal">Aust Fam Physician</span>
|
||
1979 Feb;8(2):179-94.
|
||
<span class="bold">PMID: </span><a href="/pubmed/106817" target="_blank">106817</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20temporal%20lobe%20epilepsy%208%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 (53)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/16832669">Temporal lobe resections.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harkness W</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2006 Aug;22(8):936-44.
|
||
Epub 2006 Jul 11
|
||
doi: 10.1007/s00381-006-0140-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16832669" target="_blank">16832669</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12391356">Exercise-induced temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sturm JW,
|
||
Fedi M,
|
||
Berkovic SF,
|
||
Reutens DC</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2002 Oct 22;59(8):1246-8.
|
||
doi: 10.1212/wnl.59.8.1246.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12391356" target="_blank">12391356</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10487198">Benign childhood epilepsy with centrotemporal spikes and hippocampal atrophy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gelisse P,
|
||
Genton P,
|
||
Raybaud C,
|
||
Thiry A,
|
||
Pincemaille O</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
1999 Sep;40(9):1312-5.
|
||
doi: 10.1111/j.1528-1157.1999.tb00864.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10487198" target="_blank">10487198</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9633726">Nocturnal temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bernasconi A,
|
||
Andermann F,
|
||
Cendes F,
|
||
Dubeau F,
|
||
Andermann E,
|
||
Olivier A</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
1998 Jun;50(6):1772-7.
|
||
doi: 10.1212/wnl.50.6.1772.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9633726" target="_blank">9633726</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/106817">Epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gilligan B</span><br />
|
||
<span class="medgenPMjournal">Aust Fam Physician</span>
|
||
1979 Feb;8(2):179-94.
|
||
<span class="bold">PMID: </span><a href="/pubmed/106817" target="_blank">106817</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20temporal%20lobe%20epilepsy%208%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (25)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/18004642">Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Striano P,
|
||
Gambardella A,
|
||
Coppola A,
|
||
Di Bonaventura C,
|
||
Bovo G,
|
||
Diani E,
|
||
Boaretto F,
|
||
Egeo G,
|
||
Ciampa C,
|
||
Labate A,
|
||
Testoni S,
|
||
Passarelli D,
|
||
Manna I,
|
||
Sferro C,
|
||
Aguglia U,
|
||
Caranci F,
|
||
Giallonardo AT,
|
||
Striano S,
|
||
Nobile C,
|
||
Michelucci R</span><br />
|
||
<span class="medgenPMjournal">J Neurol</span>
|
||
2008 Jan;255(1):16-23.
|
||
Epub 2007 Nov 21
|
||
doi: 10.1007/s00415-007-0653-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/18004642" target="_blank">18004642</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16832669">Temporal lobe resections.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harkness W</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2006 Aug;22(8):936-44.
|
||
Epub 2006 Jul 11
|
||
doi: 10.1007/s00381-006-0140-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16832669" target="_blank">16832669</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11306771">Prestroke dementia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Barba R,
|
||
Castro MD,
|
||
del Mar Morín M,
|
||
Rodriguez-Romero R,
|
||
Rodríguez-García E,
|
||
Cantón R,
|
||
Del Ser T</span><br />
|
||
<span class="medgenPMjournal">Cerebrovasc Dis</span>
|
||
2001;11(3):216-24.
|
||
doi: 10.1159/000047642.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11306771" target="_blank">11306771</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9633726">Nocturnal temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Bernasconi A,
|
||
Andermann F,
|
||
Cendes F,
|
||
Dubeau F,
|
||
Andermann E,
|
||
Olivier A</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
1998 Jun;50(6):1772-7.
|
||
doi: 10.1212/wnl.50.6.1772.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9633726" target="_blank">9633726</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/106817">Epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Gilligan B</span><br />
|
||
<span class="medgenPMjournal">Aust Fam Physician</span>
|
||
1979 Feb;8(2):179-94.
|
||
<span class="bold">PMID: </span><a href="/pubmed/106817" target="_blank">106817</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20temporal%20lobe%20epilepsy%208%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 (37)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37806981">A comparison of comorbid headache between patients with temporal lobe epilepsy and juvenile myoclonic epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang S,
|
||
Li J,
|
||
Zhou D</span><br />
|
||
<span class="medgenPMjournal">Sci Rep</span>
|
||
2023 Oct 8;13(1):16962.
|
||
doi: 10.1038/s41598-023-43705-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37806981" target="_blank">37806981</a><a href="/pmc/articles/PMC10560662" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35972937">Characterisation of NLRP3 pathway-related neuroinflammation in temporal lobe epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pohlentz MS,
|
||
Müller P,
|
||
Cases-Cunillera S,
|
||
Opitz T,
|
||
Surges R,
|
||
Hamed M,
|
||
Vatter H,
|
||
Schoch S,
|
||
Becker AJ,
|
||
Pitsch J</span><br />
|
||
<span class="medgenPMjournal">PLoS One</span>
|
||
2022;17(8):e0271995.
|
||
Epub 2022 Aug 16
|
||
doi: 10.1371/journal.pone.0271995.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35972937" target="_blank">35972937</a><a href="/pmc/articles/PMC9380933" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34171625">Female preponderance in genetic generalized epilepsies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Videira G,
|
||
Gabriel D,
|
||
Freitas J,
|
||
Samões R,
|
||
Chorão R,
|
||
Lopes J,
|
||
Ramalheira J,
|
||
Lemos C,
|
||
Leal B,
|
||
da Silva AM,
|
||
Chaves J</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2021 Oct;91:167-171.
|
||
Epub 2021 Jun 16
|
||
doi: 10.1016/j.seizure.2021.06.014.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34171625" target="_blank">34171625</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/24315020">Suggestive linkage of familial mesial temporal lobe epilepsy to chromosome 3q26.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Fanciulli M,
|
||
Di Bonaventura C,
|
||
Egeo G,
|
||
Fattouch J,
|
||
Dazzo E,
|
||
Radovic S,
|
||
Spadotto A,
|
||
Giallonardo AT,
|
||
Nobile C</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Res</span>
|
||
2014 Feb;108(2):232-40.
|
||
Epub 2013 Nov 18
|
||
doi: 10.1016/j.eplepsyres.2013.11.002.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24315020" target="_blank">24315020</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16832669">Temporal lobe resections.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Harkness W</span><br />
|
||
<span class="medgenPMjournal">Childs Nerv Syst</span>
|
||
2006 Aug;22(8):936-44.
|
||
Epub 2006 Jul 11
|
||
doi: 10.1007/s00381-006-0140-5.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16832669" target="_blank">16832669</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20temporal%20lobe%20epilepsy%208%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 (44)</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/36219914">Systematic review and patient-level meta-analysis of radiofrequency ablation for medically refractory epilepsy: Implications for clinical practice and research.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kerezoudis P,
|
||
Tsayem IN,
|
||
Lundstrom BN,
|
||
Van Gompel JJ</span><br />
|
||
<span class="medgenPMjournal">Seizure</span>
|
||
2022 Nov;102:113-119.
|
||
Epub 2022 Oct 4
|
||
doi: 10.1016/j.seizure.2022.10.003.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36219914" target="_blank">36219914</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20temporal%20lobe%20epilepsy%208%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 (1)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
</div>
|
||
<div class=" bottom">
|
||
|
||
</div>
|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
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|
||
|
||
<!-- MedGen supplemental column starts here -->
|
||
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|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Genetic_Testing_Registry">Genetic Testing Registry</h1><a sid="106" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="/gtr/tests?term=C4225318%5bDISCUI%5d&filter=method%3A2%5F7" target="_blank">Sequence analysis of the entire coding region (3)</a></li>
|
||
<li class="portletSeeAll portletSeeAllPad"><total><a href="/gtr/tests?term=C4225318%5bDISCUI%5d" target="_blank">See all (3)</a></total></li>
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<div class="portlet_content ln"><ul><li><a href="https://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=616461" target="_blank">OMIM</a></li><li><a href="https://clinicaltrials.gov/search?cond=Familial%20temporal%20lobe%20epilepsy%208" target="_blank">ClinicalTrials.gov</a></li></ul></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=(familial%20temporal%20lobe%20epilepsy%208)%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(%22Familial%20temporal%20lobe%20epilepsy%208%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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<div class="portlet_content ln"><ul><li><a href="http://www.omim.org/search?index=entry&start=1&limit=10&sort=score%20desc&field=number&search=137035" target="_blank">OMIM</a></li><li><a href="/clinvar/?term=51083[geneid]" target="_blank">View GAL variations in ClinVar</a></li><li><a href="https://catalog.coriell.org/Search?q=616461" target="_blank">Coriell Institute for Medical Research</a></li></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://www.malacards.org/card/epilepsy_familial_temporal_lobe_8" target="_blank">MalaCards</a></li><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Familial%20temporal%20lobe%20epilepsy%208" target="_blank">MedlinePlus</a></li><li><a href="https://rarediseases.info.nih.gov/diseases/16116/disease" target="_blank">NCATS Office of Rare Diseases Research (GARD)</a></li></ul></div>
|
||
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|
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|
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<div class="portlet brieflink">
|
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<a href="/pubmed/clinical?term=Familial%20temporal%20lobe%20epilepsy%208" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Familial%20temporal%20lobe%20epilepsy%208%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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<!-- MedGen supplemental column ends here -->
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<h3>Related information</h3>
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||
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<a class="brieflinkpopperctrl" href="/clinvar?LinkName=medgen_clinvar&from_uid=909158" ref="log$=recordlinks">ClinVar</a>
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<div class="brieflinkpop offscreen_noflow">Related medical variations</div>
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<a class="brieflinkpopperctrl" href="/gene?LinkName=medgen_gene_diseases&from_uid=909158" ref="log$=recordlinks">Gene</a>
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<div class="brieflinkpop offscreen_noflow">Related information in NCBI Gene</div>
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<a class="brieflinkpopperctrl" href="/gtr/tests?term=C4225318[DISCUI]" ref="log$=recordlinks">GTR</a>
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<div class="brieflinkpop offscreen_noflow">Related information in GTR</div>
|
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|
||
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||
<a class="brieflinkpopperctrl" href="/gtr/tests?term=C4225318[DISCUI]&test_type=Clinical" ref="log$=recordlinks">GTR(Clinical)</a>
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<div class="brieflinkpop offscreen_noflow">Clinical tests in GTR</div>
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<a class="brieflinkpopperctrl" href="/omim?LinkName=medgen_omim_gene&from_uid=909158" ref="log$=recordlinks">OMIM(Genes)</a>
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<a class="brieflinkpopperctrl" href="/pmc?LinkName=medgen_pmc&from_uid=909158" ref="log$=recordlinks">PMC Articles</a>
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<div class="brieflinkpop offscreen_noflow">Related information in PubMed Central Links</div>
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<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
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<a class="brieflinkpopperctrl" href="/pubmed?LinkName=medgen_pubmed_omim&from_uid=909158" ref="log$=recordlinks">PubMed (OMIM)</a>
|
||
<div class="brieflinkpop offscreen_noflow">Related literature resources in PubMed</div>
|
||
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|
||
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|
||
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<a name="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" sid="1" realname="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory" cmd="ClearHT" href="?cmd=ClearHT&" onclick="return false;" id="EntrezSystem2.PEntrez.MedGen.MedGen_ResultsPanel.HistoryDisplay.ClearHistory">
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