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<!--
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||
UID=1826100
|
||
ConceptID=C5680862
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Familial partial epilepsy</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1826100</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.">C5680862</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, partial, familial; familial partial epilepsy; hereditary partial epilepsy</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>Monarch Initiative:</td>
|
||
<td><a href="https://monarchinitiative.org/disease/MONDO:0017704" target="_blank">MONDO:0017704</a></td></tr>
|
||
<tr><td>Orphanet:</td>
|
||
<td><a target="_blank" title="Orphanet: The portal for rare diseases and orphan drugs" href="http://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=EN&Expert=309">ORPHA309</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>
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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">An instance of partial epilepsy that is caused by an inherited modification of the individual's genome. [from <a title="Monarch Initiative" href="https://monarchinitiative.org/" class="defSource" target="_blank">MONDO</a>]</div>
|
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</div>
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<div class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet 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">Familial partial epilepsy</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="matched_ds">Familial partial epilepsy</span><ul><li><span class="TLline"><a href="/medgen/325326" ref="tree=MeSH" title="MedGen record for Autosomal dominant epilepsy with auditory features">Autosomal dominant epilepsy with auditory features</a></span><ul><li><span class="TLline"><a href="/medgen/976986" ref="tree=MeSH" title="MedGen record for Adolescent/adult onset autosomal dominant epilepsy with auditory features">Adolescent/adult onset autosomal dominant epilepsy with auditory features</a></span></li><li><span class="TLline"><a href="/medgen/1643229" ref="tree=MeSH" title="MedGen record for Epilepsy, familial temporal lobe, 1">Epilepsy, familial temporal lobe, 1</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/777188" ref="tree=MeSH" title="MedGen record for Autosomal dominant nocturnal frontal lobe epilepsy">Autosomal dominant nocturnal frontal lobe epilepsy</a></span><ul><li><span class="TLline"><a href="/medgen/324932" ref="tree=MeSH" title="MedGen record for Autosomal dominant nocturnal frontal lobe epilepsy 1">Autosomal dominant nocturnal frontal lobe epilepsy 1</a></span></li><li><span class="TLline"><a href="/medgen/351053" ref="tree=MeSH" title="MedGen record for Autosomal dominant nocturnal frontal lobe epilepsy 2">Autosomal dominant nocturnal frontal lobe epilepsy 2</a></span></li><li><span class="TLline"><a href="/medgen/344263" ref="tree=MeSH" title="MedGen record for Autosomal dominant nocturnal frontal lobe epilepsy 3">Autosomal dominant nocturnal frontal lobe epilepsy 3</a></span></li><li><span class="TLline"><a href="/medgen/332082" ref="tree=MeSH" title="MedGen record for Autosomal dominant nocturnal frontal lobe epilepsy 4">Autosomal dominant nocturnal frontal lobe epilepsy 4</a></span></li><li><span class="TLline"><a href="/medgen/767220" ref="tree=MeSH" title="MedGen record for Autosomal dominant nocturnal frontal lobe epilepsy 5">Autosomal dominant nocturnal frontal lobe epilepsy 5</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1659458" ref="tree=MeSH" title="MedGen record for Benign familial mesial temporal lobe epilepsy">Benign familial mesial temporal lobe epilepsy</a></span></li><li><span class="TLline"><a href="/medgen/924120" ref="tree=MeSH" title="MedGen record for Childhood absence epilepsy">Childhood absence epilepsy</a></span></li><li><span class="TLline"><a href="/medgen/348951" ref="tree=MeSH" title="MedGen record for Familial focal epilepsy with variable foci">Familial focal epilepsy with variable foci</a></span><ul><li><span class="TLline"><a href="/medgen/1641798" ref="tree=MeSH" title="MedGen record for Epilepsy, familial focal, with variable foci 1">Epilepsy, familial focal, with variable foci 1</a></span></li><li><span class="TLline"><a href="/medgen/934676" ref="tree=MeSH" title="MedGen record for Epilepsy, familial focal, with variable foci 2">Epilepsy, familial focal, with variable foci 2</a></span></li><li><span class="TLline"><a href="/medgen/934675" ref="tree=MeSH" title="MedGen record for Epilepsy, familial focal, with variable foci 3">Epilepsy, familial focal, with variable foci 3</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1680293" ref="tree=MeSH" title="MedGen record for Familial mesial temporal lobe epilepsy with febrile seizures">Familial mesial temporal lobe epilepsy with febrile seizures</a></span></li><li><span class="TLline"><a href="/medgen/1683026" ref="tree=MeSH" title="MedGen record for Familial temporal lobe epilepsy 2">Familial temporal lobe epilepsy 2</a></span></li><li><span class="TLline"><a href="/medgen/503203" ref="tree=MeSH" title="MedGen record for Generalized epilepsy with febrile seizures plus">Generalized epilepsy with febrile seizures plus</a></span></li><li><span class="TLline"><a href="/medgen/1801137" ref="tree=MeSH" title="MedGen record for Generalized epilepsy-paroxysmal dyskinesia syndrome">Generalized epilepsy-paroxysmal dyskinesia syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1388059" ref="tree=MeSH" title="MedGen record for Juvenile absence epilepsy">Juvenile absence epilepsy</a></span></li><li><span class="TLline"><a href="/medgen/78738" ref="tree=MeSH" title="MedGen record for Juvenile myoclonic epilepsy">Juvenile myoclonic epilepsy</a></span><ul><li><span class="TLline"><a href="/medgen/442800" ref="tree=MeSH" title="MedGen record for Epilepsy, idiopathic generalized, susceptibility to, 7">Epilepsy, idiopathic generalized, susceptibility to, 7</a></span></li><li><span class="TLline"><a href="/medgen/413424" ref="tree=MeSH" title="MedGen record for Epilepsy, idiopathic generalized, susceptibility to, 9">Epilepsy, idiopathic generalized, susceptibility to, 9</a></span></li><li><span class="TLline"><a href="/medgen/414062" ref="tree=MeSH" title="MedGen record for Epilepsy, idiopathic generalized, susceptibility to, 10">Epilepsy, idiopathic generalized, susceptibility to, 10</a></span></li><li><span class="TLline"><a href="/medgen/416407" ref="tree=MeSH" title="MedGen record for Epilepsy, idiopathic generalized, susceptibility to, 11">Epilepsy, idiopathic generalized, susceptibility to, 11</a></span></li><li><span class="TLline"><a href="/medgen/861910" ref="tree=MeSH" title="MedGen record for Epilepsy, idiopathic generalized, susceptibility to, 13">Epilepsy, idiopathic generalized, susceptibility to, 13</a></span></li><li><span class="TLline"><a href="/medgen/442587" ref="tree=MeSH" title="MedGen record for Epilepsy, juvenile myoclonic, susceptibility to, 6">Epilepsy, juvenile myoclonic, susceptibility to, 6</a></span></li><li><span class="TLline"><a href="/medgen/416408" ref="tree=MeSH" title="MedGen record for EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8">EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 8</a></span></li><li><span class="TLline"><a href="/medgen/887102" ref="tree=MeSH" title="MedGen record for Juvenile Myoclonic Epilepsy, Intractable, without Status Epilepticus">Juvenile Myoclonic Epilepsy, Intractable, without Status Epilepticus</a></span></li><li><span class="TLline"><a href="/medgen/342587" ref="tree=MeSH" title="MedGen record for Myoclonic epilepsy, juvenile, susceptibility to, 1">Myoclonic epilepsy, juvenile, susceptibility to, 1</a></span></li><li><span class="TLline"><a href="/medgen/324732" ref="tree=MeSH" title="MedGen record for Myoclonic epilepsy, juvenile, susceptibility to, 3">Myoclonic epilepsy, juvenile, susceptibility to, 3</a></span></li><li><span class="TLline"><a href="/medgen/370067" ref="tree=MeSH" title="MedGen record for Myoclonic epilepsy, juvenile, susceptibility to, 4">Myoclonic epilepsy, juvenile, susceptibility to, 4</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1659013" ref="tree=MeSH" title="MedGen record for Mesial temporal lobe epilepsy with hippocampal sclerosis">Mesial temporal lobe epilepsy with hippocampal sclerosis</a></span></li><li><span class="TLline"><a href="/medgen/138210" ref="tree=MeSH" title="MedGen record for Self-limited epilepsy with centrotemporal spikes">Self-limited epilepsy with centrotemporal spikes</a></span><ul><li><span class="TLline"><a href="/medgen/432274" ref="tree=MeSH" title="MedGen record for Benign Rolandic epilepsy">Benign Rolandic epilepsy</a></span></li><li><span class="TLline"><a href="/medgen/79465" ref="tree=MeSH" title="MedGen record for Landau-Kleffner syndrome">Landau-Kleffner syndrome</a></span></li></ul></li></ul></li></ul></div></div></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/38881224">Clinical and Molecular Profiling in GNAO1 Permits Phenotype-Genotype Correlation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lasa-Aranzasti A,
|
||
Larasati YA,
|
||
da Silva Cardoso J,
|
||
Solis GP,
|
||
Koval A,
|
||
Cazurro-Gutiérrez A,
|
||
Ortigoza-Escobar JD,
|
||
Miranda MC,
|
||
De la Casa-Fages B,
|
||
Moreno-Galdó A,
|
||
Tizzano EF,
|
||
Gómez-Andrés D,
|
||
Verdura E,
|
||
Katanaev VL,
|
||
Pérez-Dueñas B;
|
||
Study Group of GNAO1 patients from Spain</span><br />
|
||
<span class="medgenPMjournal">Mov Disord</span>
|
||
2024 Sep;39(9):1578-1591.
|
||
Epub 2024 Jun 16
|
||
doi: 10.1002/mds.29881.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38881224" target="_blank">38881224</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/38748979">Teratogenesis, Perinatal, and Neurodevelopmental Outcomes After In Utero Exposure to Antiseizure Medication: Practice Guideline From the AAN, AES, and SMFM.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Pack AM,
|
||
Oskoui M,
|
||
Williams Roberson S,
|
||
Donley DK,
|
||
French J,
|
||
Gerard EE,
|
||
Gloss D,
|
||
Miller WR,
|
||
Munger Clary HM,
|
||
Osmundson SS,
|
||
McFadden B,
|
||
Parratt K,
|
||
Pennell PB,
|
||
Saade G,
|
||
Smith DB,
|
||
Sullivan K,
|
||
Thomas SV,
|
||
Tomson T,
|
||
Dolan O'Brien M,
|
||
Botchway-Doe K,
|
||
Silsbee HM,
|
||
Keezer MR</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2024 Jun;102(11):e209279.
|
||
Epub 2024 May 15
|
||
doi: 10.1212/WNL.0000000000209279.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38748979" target="_blank">38748979</a><a href="/pmc/articles/PMC11175651" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/37710171">International consensus recommendations for the identification and treatment of tuberous sclerosis complex-associated neuropsychiatric disorders (TAND).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">de Vries PJ,
|
||
Heunis TM,
|
||
Vanclooster S,
|
||
Chambers N,
|
||
Bissell S,
|
||
Byars AW,
|
||
Flinn J,
|
||
Gipson TT,
|
||
van Eeghen AM,
|
||
Waltereit R,
|
||
Capal JK,
|
||
Cukier S,
|
||
Davis PE,
|
||
Smith C,
|
||
Kingswood JC,
|
||
Schoeters E,
|
||
Srivastava S,
|
||
Takei M,
|
||
Gardner-Lubbe S,
|
||
Kumm AJ,
|
||
Krueger DA,
|
||
Sahin M,
|
||
De Waele L,
|
||
Jansen AC</span><br />
|
||
<span class="medgenPMjournal">J Neurodev Disord</span>
|
||
2023 Sep 14;15(1):32.
|
||
doi: 10.1186/s11689-023-09500-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37710171" target="_blank">37710171</a><a href="/pmc/articles/PMC10503032" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(familial%20partial%20epilepsy)%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 (43)</a></div><h3 class="subhead">Curated<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpCurated"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3><h3 class="nl vspace"><a href="https://www.nice.org.uk/guidance/ng217" target="_blank">UK NICE Guideline NG217, Epilepsies in children, young people and adults, 2022</a></h3>
|
||
</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/22151702">Mosaic SCN1A mutations in familial partial epilepsy with antecedent febrile seizures.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Shi YW,
|
||
Yu MJ,
|
||
Long YS,
|
||
Qin B,
|
||
He N,
|
||
Meng H,
|
||
Liu XR,
|
||
Deng WY,
|
||
Gao MM,
|
||
Yi YH,
|
||
Li BM,
|
||
Liao WP</span><br />
|
||
<span class="medgenPMjournal">Genes Brain Behav</span>
|
||
2012 Mar;11(2):170-6.
|
||
Epub 2011 Dec 14
|
||
doi: 10.1111/j.1601-183X.2011.00756.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22151702" target="_blank">22151702</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20478764">Malignant autosomal dominant frontal lobe epilepsy with repeated episodes of status epilepticus: successful treatment with vagal nerve stimulation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carreño M,
|
||
Garcia-Alvarez D,
|
||
Maestro I,
|
||
Fernández S,
|
||
Donaire A,
|
||
Boget T,
|
||
Rumià J,
|
||
Pintor L,
|
||
Setoain X</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2010 Jun;12(2):155-8.
|
||
Epub 2010 May 18
|
||
doi: 10.1684/epd.2010.0307.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20478764" target="_blank">20478764</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16359475">Genetic focal epilepsies: state of the art and paths to the future.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Andermann F,
|
||
Kobayashi E,
|
||
Andermann E</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2005;46 Suppl 10:61-7.
|
||
doi: 10.1111/j.1528-1167.2005.00361.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16359475" target="_blank">16359475</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11887964">Progress in the genetics of the partial epilepsies.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ottman R</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2001;42 Suppl 5(Suppl 5):24-30.
|
||
doi: 10.1046/j.1528-1157.2001.0420s5024.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11887964" target="_blank">11887964</a><a href="/pmc/articles/PMC2737452" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9851433">Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Scheffer IE,
|
||
Phillips HA,
|
||
O'Brien CE,
|
||
Saling MM,
|
||
Wrennall JA,
|
||
Wallace RH,
|
||
Mulley JC,
|
||
Berkovic SF</span><br />
|
||
<span class="medgenPMjournal">Ann Neurol</span>
|
||
1998 Dec;44(6):890-9.
|
||
doi: 10.1002/ana.410440607.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9851433" target="_blank">9851433</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20partial%20epilepsy%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 (6)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/20659149">Familial partial epilepsy with variable foci: a new family with suggestion of linkage to chromosome 22q12.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Morales-Corraliza J,
|
||
Gómez-Garre P,
|
||
Sanz R,
|
||
Díaz-Otero F,
|
||
Gutiérrez-Delicado E,
|
||
Serratosa JM</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2010 Sep;51(9):1910-4.
|
||
doi: 10.1111/j.1528-1167.2010.02680.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20659149" target="_blank">20659149</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16359475">Genetic focal epilepsies: state of the art and paths to the future.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Andermann F,
|
||
Kobayashi E,
|
||
Andermann E</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2005;46 Suppl 10:61-7.
|
||
doi: 10.1111/j.1528-1167.2005.00361.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16359475" target="_blank">16359475</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15329069">Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Berkovic SF,
|
||
Serratosa JM,
|
||
Phillips HA,
|
||
Xiong L,
|
||
Andermann E,
|
||
Díaz-Otero F,
|
||
Gómez-Garre P,
|
||
Martín M,
|
||
Fernández-Bullido Y,
|
||
Andermann F,
|
||
Lopes-Cendes I,
|
||
Dubeau F,
|
||
Desbiens R,
|
||
Scheffer IE,
|
||
Wallace RH,
|
||
Mulley JC,
|
||
Pandolfo M</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2004 Sep;45(9):1054-60.
|
||
doi: 10.1111/j.0013-9580.2004.30502.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15329069" target="_blank">15329069</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14510823">Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Callenbach PM,
|
||
van den Maagdenberg AM,
|
||
Hottenga JJ,
|
||
van den Boogerd EH,
|
||
de Coo RF,
|
||
Lindhout D,
|
||
Frants RR,
|
||
Sandkuijl LA,
|
||
Brouwer OF</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2003 Oct;44(10):1298-305.
|
||
doi: 10.1046/j.1528-1157.2003.62302.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14510823" target="_blank">14510823</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10961632">Familial aphasic episodes: another variant of partial epilepsy with simple inheritance?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kanemoto K,
|
||
Kawasaki J</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2000 Aug;41(8):1036-8.
|
||
doi: 10.1111/j.1528-1157.2000.tb00290.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10961632" target="_blank">10961632</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20partial%20epilepsy%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 (9)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/20478764">Malignant autosomal dominant frontal lobe epilepsy with repeated episodes of status epilepticus: successful treatment with vagal nerve stimulation.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Carreño M,
|
||
Garcia-Alvarez D,
|
||
Maestro I,
|
||
Fernández S,
|
||
Donaire A,
|
||
Boget T,
|
||
Rumià J,
|
||
Pintor L,
|
||
Setoain X</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2010 Jun;12(2):155-8.
|
||
Epub 2010 May 18
|
||
doi: 10.1684/epd.2010.0307.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20478764" target="_blank">20478764</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16359475">Genetic focal epilepsies: state of the art and paths to the future.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Andermann F,
|
||
Kobayashi E,
|
||
Andermann E</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2005;46 Suppl 10:61-7.
|
||
doi: 10.1111/j.1528-1167.2005.00361.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16359475" target="_blank">16359475</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12011300">Familial temporal lobe epilepsy with febrile seizures.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Depondt C,
|
||
Van Paesschen W,
|
||
Matthijs G,
|
||
Legius E,
|
||
Martens K,
|
||
Demaerel P,
|
||
Wilms G</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2002 May 14;58(9):1429-33.
|
||
doi: 10.1212/wnl.58.9.1429.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12011300" target="_blank">12011300</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20partial%20epilepsy%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 (3)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29630124">Study of candidate gene cHRNA4 for familial epilepsy syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wang N,
|
||
Huang HL,
|
||
Zhou H</span><br />
|
||
<span class="medgenPMjournal">Eur Rev Med Pharmacol Sci</span>
|
||
2018 Mar;22(6):1765-1769.
|
||
doi: 10.26355/eurrev_201803_14594.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29630124" target="_blank">29630124</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20659149">Familial partial epilepsy with variable foci: a new family with suggestion of linkage to chromosome 22q12.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Morales-Corraliza J,
|
||
Gómez-Garre P,
|
||
Sanz R,
|
||
Díaz-Otero F,
|
||
Gutiérrez-Delicado E,
|
||
Serratosa JM</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2010 Sep;51(9):1910-4.
|
||
doi: 10.1111/j.1528-1167.2010.02680.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20659149" target="_blank">20659149</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15329069">Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Berkovic SF,
|
||
Serratosa JM,
|
||
Phillips HA,
|
||
Xiong L,
|
||
Andermann E,
|
||
Díaz-Otero F,
|
||
Gómez-Garre P,
|
||
Martín M,
|
||
Fernández-Bullido Y,
|
||
Andermann F,
|
||
Lopes-Cendes I,
|
||
Dubeau F,
|
||
Desbiens R,
|
||
Scheffer IE,
|
||
Wallace RH,
|
||
Mulley JC,
|
||
Pandolfo M</span><br />
|
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<span class="medgenPMjournal">Epilepsia</span>
|
||
2004 Sep;45(9):1054-60.
|
||
doi: 10.1111/j.0013-9580.2004.30502.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15329069" target="_blank">15329069</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/14510823">Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Callenbach PM,
|
||
van den Maagdenberg AM,
|
||
Hottenga JJ,
|
||
van den Boogerd EH,
|
||
de Coo RF,
|
||
Lindhout D,
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Frants RR,
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||
Sandkuijl LA,
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Brouwer OF</span><br />
|
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<span class="medgenPMjournal">Epilepsia</span>
|
||
2003 Oct;44(10):1298-305.
|
||
doi: 10.1046/j.1528-1157.2003.62302.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/14510823" target="_blank">14510823</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/10577924">Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Xiong L,
|
||
Labuda M,
|
||
Li DS,
|
||
Hudson TJ,
|
||
Desbiens R,
|
||
Patry G,
|
||
Verret S,
|
||
Langevin P,
|
||
Mercho S,
|
||
Seni MH,
|
||
Scheffer I,
|
||
Dubeau F,
|
||
Berkovic SF,
|
||
Andermann F,
|
||
Andermann E,
|
||
Pandolfo M</span><br />
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||
<span class="medgenPMjournal">Am J Hum Genet</span>
|
||
1999 Dec;65(6):1698-710.
|
||
doi: 10.1086/302649.
|
||
<span class="bold">PMID: </span><a href="/pubmed/10577924" target="_blank">10577924</a><a href="/pmc/articles/PMC1288381" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Familial%20partial%20epilepsy%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 (6)</a></div></div>
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