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<!--
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UID=866862
|
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ConceptID=C4021217
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">EEG with generalized slow activity</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>866862</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.">C4021217</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>EEG with generalised slow activity; EEG: generalised slow activity; EEG: generalized slow activity</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
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<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0010845">HP:0010845</a></td></tr>
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<div class="portlet mgSection" id="ID_100">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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||
<div class="portlet_content ln">Diffuse slowing of cerebral electrical activity recorded along the scalp by electroencephalography (EEG). [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="TLline">EEG with generalized slow activity</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/105425" ref="tree=MeSH" title="MedGen record for Abnormality of the nervous system">Abnormality of the nervous system</a></span><ul><li><span class="TLline"><a href="/medgen/868417" ref="tree=MeSH" title="MedGen record for Abnormal nervous system physiology">Abnormal nervous system physiology</a></span><ul><li><span class="TLline"><a href="/medgen/867410" ref="tree=MeSH" title="MedGen record for Abnormal nervous system electrophysiology">Abnormal nervous system electrophysiology</a></span><ul><li><span class="TLline"><a href="/medgen/868205" ref="tree=MeSH" title="MedGen record for Abnormality of central nervous system electrophysiology">Abnormality of central nervous system electrophysiology</a></span><ul><li><span class="TLline"><a href="/medgen/56235" ref="tree=MeSH" title="MedGen record for EEG abnormality">EEG abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/869053" ref="tree=MeSH" title="MedGen record for EEG with abnormally slow frequencies">EEG with abnormally slow frequencies</a></span><ul><li><span class="matched_ds">EEG with generalized slow activity</span><ul><li><span class="TLline"><a href="/medgen/869052" ref="tree=MeSH" title="MedGen record for EEG with continuous slow activity">EEG with continuous slow activity</a></span></li><li><span class="TLline"><a href="/medgen/869050" ref="tree=MeSH" title="MedGen record for EEG with generalized slow activity grade 1">EEG with generalized slow activity grade 1</a></span></li><li><span class="TLline"><a href="/medgen/869049" ref="tree=MeSH" title="MedGen record for EEG with generalized slow activity grade 2">EEG with generalized slow activity grade 2</a></span></li><li><span class="TLline"><a href="/medgen/869048" ref="tree=MeSH" title="MedGen record for EEG with generalized slow activity grade 3">EEG with generalized slow activity grade 3</a></span></li><li><span class="TLline"><a href="/medgen/866844" ref="tree=MeSH" title="MedGen record for EEG with generalized slow activity grade 4">EEG with generalized slow activity grade 4</a></span></li><li><span class="TLline"><a href="/medgen/869051" ref="tree=MeSH" title="MedGen record for EEG with intermittent slow activity">EEG with intermittent slow activity</a></span></li></ul></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>
|
||
<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_116041"><div><strong>Cholestanol storage disease</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>116041</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:">C0238052</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cerebrotendinous xanthomatosis (CTX) is a lipid storage disease characterized by infantile-onset diarrhea, childhood-onset cataract, adolescent- to young adult-onset tendon xanthomas, and adult-onset progressive neurologic dysfunction (dementia, psychiatric disturbances, pyramidal and/or cerebellar signs, dystonia, atypical parkinsonism, peripheral neuropathy, and seizures). Chronic diarrhea from infancy and/or neonatal cholestasis may be the earliest clinical manifestation. In approximately 75% of affected individuals, cataracts are the first finding, often appearing in the first decade of life. Xanthomas appear in the second or third decade; they occur on the Achilles tendon, the extensor tendons of the elbow and hand, the patellar tendon, and the neck tendons. Xanthomas have been reported in the lung, bones, and central nervous system. Some individuals show cognitive impairment from early infancy, whereas the majority have normal or only slightly impaired intellectual function until puberty; dementia with slow deterioration in intellectual abilities occurs in the third decade in more than 50% of individuals. Neuropsychiatric symptoms such as behavioral changes, hallucinations, agitation, aggression, depression, and suicide attempts may be prominent. Pyramidal signs (i.e., spasticity) and/or cerebellar signs almost invariably become evident between ages 20 and 30 years. The biochemical abnormalities that distinguish CTX from other conditions with xanthomas include high plasma and tissue cholestanol concentration, normal-to-low plasma cholesterol concentration, decreased chenodeoxycholic acid (CDCA), increased concentration of bile alcohols and their glyconjugates, and increased concentrations of cholestanol and apolipoprotein B in cerebrospinal fluid.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/116041">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_163232"><div><strong>X-linked intellectual disability-psychosis-macroorchidism syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>163232</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.">C0796222</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The spectrum of MECP2-related phenotypes in females ranges from classic Rett syndrome to variant Rett syndrome with a broader clinical phenotype (either milder or more severe than classic Rett syndrome) to mild learning disabilities; the spectrum in males ranges from severe neonatal encephalopathy to pyramidal signs, parkinsonism, and macroorchidism (PPM-X) syndrome to severe syndromic/nonsyndromic intellectual disability. Females: Classic Rett syndrome, a progressive neurodevelopmental disorder primarily affecting girls, is characterized by apparently normal psychomotor development during the first six to 18 months of life, followed by a short period of developmental stagnation, then rapid regression in language and motor skills, followed by long-term stability. During the phase of rapid regression, repetitive, stereotypic hand movements replace purposeful hand use. Additional findings include fits of screaming and inconsolable crying, autistic features, panic-like attacks, bruxism, episodic apnea and/or hyperpnea, gait ataxia and apraxia, tremors, seizures, and acquired microcephaly. Males: Severe neonatal-onset encephalopathy, the most common phenotype in affected males, is characterized by a relentless clinical course that follows a metabolic-degenerative type of pattern, abnormal tone, involuntary movements, severe seizures, and breathing abnormalities. Death often occurs before age two years.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/163232">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1645968"><div><strong>Neurodevelopmental disorder with or without seizures and gait abnormalities</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1645968</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.">C4693391</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with or without seizures and gait abnormalities (NEDSGA) is an autosomal dominant disorder characterized by global developmental delay apparent from infancy or early childhood, resulting in variably impaired intellectual development that can range from profound with absent speech to mild with an ability to attend special schools. Most affected individuals show irritability, stiffness, and hypertonia early in life, which progresses to spasticity and impaired gait later. Some patients may develop seizures of variable severity early in life (summary by Martin et al., 2017).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1645968">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1663579"><div><strong>Developmental and epileptic encephalopathy, 2</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1663579</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.">C4750718</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">CDKL5 deficiency disorder (CDD) is a developmental and epileptic encephalopathy (DEE) characterized by severe early-onset intractable epilepsy and motor, cognitive, visual, and autonomic disturbances. Movement disorders include chorea, dystonia, and stereotypical hand and leg movements. Although females are more commonly affected than males (female-to-male ratio is approximately 4:1), the severity of manifestations in heterozygous females and hemizygous males can be equivalent. However, the severity of the phenotype can vary depending on the type and position of the CDKL5 pathogenic variant, pattern of X-chromosome inactivation in females, and presence of postzygotic mosaicism in males or females, who can have mild manifestations.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1663579">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684142"><div><strong>Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684142</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.">C5193057</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination (NEDMEHM) is an autosomal recessive neurometabolic disorder characterized by these cardinal features. Patients also show an exaggerated startle reflex in early infancy (Rodan et al., 2018).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684142">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1823963"><div><strong>Developmental and epileptic encephalopathy 105 with hypopituitarism</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1823963</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.">C5774190</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Developmental and epileptic encephalopathy-105 with hypopituitarism (DEE105) is an autosomal recessive disorder characterized by the onset of seizures and pituitary insufficiency in the first weeks or months of life. Affected individuals have profoundly impaired development with almost no acquisition of skills. They are hypotonic, unable to sit or speak, and have poor or absent visual fixation. Endocrine workup shows central pituitary dysfunction with low hormone levels. Brain imaging shows cerebral atrophy, thin corpus callosum, and small pituitary gland (Schanzer et al., 2021). For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1823963">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_116041" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Cholestanol storage disease</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1823963" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy 105 with hypopituitarism</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1663579" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy, 2</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684142" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1645968" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Neurodevelopmental disorder with or without seizures and gait abnormalities</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_163232" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">X-linked intellectual disability-psychosis-macroorchidism syndrome</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/35131107">Medical treatment of Rasmussen's Encephalitis: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lagarde S,
|
||
Boucraut J,
|
||
Bartolomei F</span><br />
|
||
<span class="medgenPMjournal">Rev Neurol (Paris)</span>
|
||
2022 Sep;178(7):675-691.
|
||
Epub 2022 Feb 4
|
||
doi: 10.1016/j.neurol.2022.01.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35131107" target="_blank">35131107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32090418">European Academy of Neurology guideline on the diagnosis of coma and other disorders of consciousness.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kondziella D,
|
||
Bender A,
|
||
Diserens K,
|
||
van Erp W,
|
||
Estraneo A,
|
||
Formisano R,
|
||
Laureys S,
|
||
Naccache L,
|
||
Ozturk S,
|
||
Rohaut B,
|
||
Sitt JD,
|
||
Stender J,
|
||
Tiainen M,
|
||
Rossetti AO,
|
||
Gosseries O,
|
||
Chatelle C;
|
||
EAN Panel on Coma, Disorders of Consciousness</span><br />
|
||
<span class="medgenPMjournal">Eur J Neurol</span>
|
||
2020 May;27(5):741-756.
|
||
Epub 2020 Feb 23
|
||
doi: 10.1111/ene.14151.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32090418" target="_blank">32090418</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22713136">The diagnosis and treatment of limbic encephalitis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Asztely F,
|
||
Kumlien E</span><br />
|
||
<span class="medgenPMjournal">Acta Neurol Scand</span>
|
||
2012 Dec;126(6):365-75.
|
||
Epub 2012 Jun 19
|
||
doi: 10.1111/j.1600-0404.2012.01691.x.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22713136" target="_blank">22713136</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(eeg%20with%20generalized%20slow%20activity)%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 (17)</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/38135915">Developmental epileptic encephalopathy in DLG4-related synaptopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kassabian B,
|
||
Levy AM,
|
||
Gardella E,
|
||
Aledo-Serrano A,
|
||
Ananth AL,
|
||
Brea-Fernández AJ,
|
||
Caumes R,
|
||
Chatron N,
|
||
Dainelli A,
|
||
De Wachter M,
|
||
Denommé-Pichon AS,
|
||
Dye TJ,
|
||
Fazzi E,
|
||
Felt R,
|
||
Fernández-Jaén A,
|
||
Fernández-Prieto M,
|
||
Gantz E,
|
||
Gasperowicz P,
|
||
Gil-Nagel A,
|
||
Gómez-Andrés D,
|
||
Greiner HM,
|
||
Guerrini R,
|
||
Haanpää MK,
|
||
Helin M,
|
||
Hoyer J,
|
||
Hurst ACE,
|
||
Kallish S,
|
||
Karkare SN,
|
||
Khan A,
|
||
Kleinendorst L,
|
||
Koch J,
|
||
Kothare SV,
|
||
Koudijs SM,
|
||
Lagae L,
|
||
Lakeman P,
|
||
Leppig KA,
|
||
Lesca G,
|
||
Lopergolo D,
|
||
Lusk L,
|
||
Mackenzie A,
|
||
Mei D,
|
||
Møller RS,
|
||
Pereira EM,
|
||
Platzer K,
|
||
Quelin C,
|
||
Revah-Politi A,
|
||
Rheims S,
|
||
Rodríguez-Palmero A,
|
||
Rossi A,
|
||
Santorelli F,
|
||
Seinfeld S,
|
||
Sell E,
|
||
Stephenson D,
|
||
Szczaluba K,
|
||
Trinka E,
|
||
Umair M,
|
||
Van Esch H,
|
||
van Haelst MM,
|
||
Veenma DCM,
|
||
Weber S,
|
||
Weckhuysen S,
|
||
Zacher P,
|
||
Tümer Z,
|
||
Rubboli G</span><br />
|
||
<span class="medgenPMjournal">Epilepsia</span>
|
||
2024 Apr;65(4):1029-1045.
|
||
Epub 2024 Feb 29
|
||
doi: 10.1111/epi.17876.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38135915" target="_blank">38135915</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36281767">Precuneus magnetic stimulation for Alzheimer's disease: a randomized, sham-controlled trial.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koch G,
|
||
Casula EP,
|
||
Bonnì S,
|
||
Borghi I,
|
||
Assogna M,
|
||
Minei M,
|
||
Pellicciari MC,
|
||
Motta C,
|
||
D'Acunto A,
|
||
Porrazzini F,
|
||
Maiella M,
|
||
Ferrari C,
|
||
Caltagirone C,
|
||
Santarnecchi E,
|
||
Bozzali M,
|
||
Martorana A</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2022 Nov 21;145(11):3776-3786.
|
||
doi: 10.1093/brain/awac285.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36281767" target="_blank">36281767</a><a href="/pmc/articles/PMC9679166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34668959">Sleep and longitudinal cognitive performance in preclinical and early symptomatic Alzheimer's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lucey BP,
|
||
Wisch J,
|
||
Boerwinkle AH,
|
||
Landsness EC,
|
||
Toedebusch CD,
|
||
McLeland JS,
|
||
Butt OH,
|
||
Hassenstab J,
|
||
Morris JC,
|
||
Ances BM,
|
||
Holtzman DM</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2021 Oct 22;144(9):2852-2862.
|
||
doi: 10.1093/brain/awab272.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34668959" target="_blank">34668959</a><a href="/pmc/articles/PMC8536939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29124439">Lennox-Gastaut syndrome: a comprehensive review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Asadi-Pooya AA</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2018 Mar;39(3):403-414.
|
||
Epub 2017 Nov 9
|
||
doi: 10.1007/s10072-017-3188-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29124439" target="_blank">29124439</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8848969">Epileptic negative myoclonus.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Tassinari CA,
|
||
Rubboli G,
|
||
Parmeggiani L,
|
||
Valzania F,
|
||
Plasmati R,
|
||
Riguzzi P,
|
||
Michelucci R,
|
||
Volpi L,
|
||
Passarelli D,
|
||
Meletti S</span><br />
|
||
<span class="medgenPMjournal">Adv Neurol</span>
|
||
1995;67:181-97.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8848969" target="_blank">8848969</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22EEG%20with%20generalized%20slow%20activity%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 (348)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35131107">Medical treatment of Rasmussen's Encephalitis: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lagarde S,
|
||
Boucraut J,
|
||
Bartolomei F</span><br />
|
||
<span class="medgenPMjournal">Rev Neurol (Paris)</span>
|
||
2022 Sep;178(7):675-691.
|
||
Epub 2022 Feb 4
|
||
doi: 10.1016/j.neurol.2022.01.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35131107" target="_blank">35131107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33726524">Sleep Abnormalities in Schizophrenia: State of the Art and Next Steps.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ferrarelli F</span><br />
|
||
<span class="medgenPMjournal">Am J Psychiatry</span>
|
||
2021 Oct 1;178(10):903-913.
|
||
Epub 2021 Mar 17
|
||
doi: 10.1176/appi.ajp.2020.20070968.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33726524" target="_blank">33726524</a><a href="/pmc/articles/PMC8446088" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32090418">European Academy of Neurology guideline on the diagnosis of coma and other disorders of consciousness.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kondziella D,
|
||
Bender A,
|
||
Diserens K,
|
||
van Erp W,
|
||
Estraneo A,
|
||
Formisano R,
|
||
Laureys S,
|
||
Naccache L,
|
||
Ozturk S,
|
||
Rohaut B,
|
||
Sitt JD,
|
||
Stender J,
|
||
Tiainen M,
|
||
Rossetti AO,
|
||
Gosseries O,
|
||
Chatelle C;
|
||
EAN Panel on Coma, Disorders of Consciousness</span><br />
|
||
<span class="medgenPMjournal">Eur J Neurol</span>
|
||
2020 May;27(5):741-756.
|
||
Epub 2020 Feb 23
|
||
doi: 10.1111/ene.14151.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32090418" target="_blank">32090418</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29124439">Lennox-Gastaut syndrome: a comprehensive review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Asadi-Pooya AA</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2018 Mar;39(3):403-414.
|
||
Epub 2017 Nov 9
|
||
doi: 10.1007/s10072-017-3188-y.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29124439" target="_blank">29124439</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26899133">Coffee, caffeine, and sleep: A systematic review of epidemiological studies and randomized controlled trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clark I,
|
||
Landolt HP</span><br />
|
||
<span class="medgenPMjournal">Sleep Med Rev</span>
|
||
2017 Feb;31:70-78.
|
||
Epub 2016 Jan 30
|
||
doi: 10.1016/j.smrv.2016.01.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26899133" target="_blank">26899133</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22EEG%20with%20generalized%20slow%20activity%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 (421)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36281767">Precuneus magnetic stimulation for Alzheimer's disease: a randomized, sham-controlled trial.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koch G,
|
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Casula EP,
|
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Bonnì S,
|
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Borghi I,
|
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Assogna M,
|
||
Minei M,
|
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Pellicciari MC,
|
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Motta C,
|
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D'Acunto A,
|
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Porrazzini F,
|
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Maiella M,
|
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Ferrari C,
|
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Caltagirone C,
|
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Santarnecchi E,
|
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Bozzali M,
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Martorana A</span><br />
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<span class="medgenPMjournal">Brain</span>
|
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2022 Nov 21;145(11):3776-3786.
|
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doi: 10.1093/brain/awac285.
|
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<span class="bold">PMID: </span><a href="/pubmed/36281767" target="_blank">36281767</a><a href="/pmc/articles/PMC9679166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32049738">Chance and risk in epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baud MO,
|
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Proix T,
|
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Rao VR,
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Schindler K</span><br />
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<span class="medgenPMjournal">Curr Opin Neurol</span>
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2020 Apr;33(2):163-172.
|
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doi: 10.1097/WCO.0000000000000798.
|
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<span class="bold">PMID: </span><a href="/pubmed/32049738" target="_blank">32049738</a></div>
|
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|
||
<div class="nl"><a target="_blank" href="/pubmed/26899133">Coffee, caffeine, and sleep: A systematic review of epidemiological studies and randomized controlled trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clark I,
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Landolt HP</span><br />
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<span class="medgenPMjournal">Sleep Med Rev</span>
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2017 Feb;31:70-78.
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<span class="bold">PMID: </span><a href="/pubmed/26899133" target="_blank">26899133</a></div>
|
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|
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<div class="nl"><a target="_blank" href="/pubmed/15054059">Human thalamic medial pulvinar nucleus is not activated during paradoxical sleep.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Magnin M,
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Bastuji H,
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Garcia-Larrea L,
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Mauguière F</span><br />
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<span class="medgenPMjournal">Cereb Cortex</span>
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2004 Aug;14(8):858-62.
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doi: 10.1093/cercor/bhh044.
|
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<span class="bold">PMID: </span><a href="/pubmed/15054059" target="_blank">15054059</a></div>
|
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|
||
<div class="nl"><a target="_blank" href="/pubmed/11520318">Epileptic encephalopathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Dulac O</span><br />
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<span class="medgenPMjournal">Epilepsia</span>
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2001;42 Suppl 3:23-6.
|
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doi: 10.1046/j.1528-1157.2001.042suppl.3023.x.
|
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<span class="bold">PMID: </span><a href="/pubmed/11520318" target="_blank">11520318</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22EEG%20with%20generalized%20slow%20activity%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 (233)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36281767">Precuneus magnetic stimulation for Alzheimer's disease: a randomized, sham-controlled trial.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koch G,
|
||
Casula EP,
|
||
Bonnì S,
|
||
Borghi I,
|
||
Assogna M,
|
||
Minei M,
|
||
Pellicciari MC,
|
||
Motta C,
|
||
D'Acunto A,
|
||
Porrazzini F,
|
||
Maiella M,
|
||
Ferrari C,
|
||
Caltagirone C,
|
||
Santarnecchi E,
|
||
Bozzali M,
|
||
Martorana A</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2022 Nov 21;145(11):3776-3786.
|
||
doi: 10.1093/brain/awac285.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36281767" target="_blank">36281767</a><a href="/pmc/articles/PMC9679166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34668959">Sleep and longitudinal cognitive performance in preclinical and early symptomatic Alzheimer's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lucey BP,
|
||
Wisch J,
|
||
Boerwinkle AH,
|
||
Landsness EC,
|
||
Toedebusch CD,
|
||
McLeland JS,
|
||
Butt OH,
|
||
Hassenstab J,
|
||
Morris JC,
|
||
Ances BM,
|
||
Holtzman DM</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2021 Oct 22;144(9):2852-2862.
|
||
doi: 10.1093/brain/awab272.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34668959" target="_blank">34668959</a><a href="/pmc/articles/PMC8536939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33726524">Sleep Abnormalities in Schizophrenia: State of the Art and Next Steps.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ferrarelli F</span><br />
|
||
<span class="medgenPMjournal">Am J Psychiatry</span>
|
||
2021 Oct 1;178(10):903-913.
|
||
Epub 2021 Mar 17
|
||
doi: 10.1176/appi.ajp.2020.20070968.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33726524" target="_blank">33726524</a><a href="/pmc/articles/PMC8446088" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32049738">Chance and risk in epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baud MO,
|
||
Proix T,
|
||
Rao VR,
|
||
Schindler K</span><br />
|
||
<span class="medgenPMjournal">Curr Opin Neurol</span>
|
||
2020 Apr;33(2):163-172.
|
||
doi: 10.1097/WCO.0000000000000798.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32049738" target="_blank">32049738</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31077993">Effects of distinctiveness and memory on lateralized and unlateralized brain-electrical activity during visual word encoding.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koppehele-Gossel J,
|
||
Khosrowtaj Z,
|
||
Gibbons H</span><br />
|
||
<span class="medgenPMjournal">Brain Cogn</span>
|
||
2019 Aug;134:9-20.
|
||
Epub 2019 May 8
|
||
doi: 10.1016/j.bandc.2019.04.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31077993" target="_blank">31077993</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22EEG%20with%20generalized%20slow%20activity%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 (259)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36281767">Precuneus magnetic stimulation for Alzheimer's disease: a randomized, sham-controlled trial.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Koch G,
|
||
Casula EP,
|
||
Bonnì S,
|
||
Borghi I,
|
||
Assogna M,
|
||
Minei M,
|
||
Pellicciari MC,
|
||
Motta C,
|
||
D'Acunto A,
|
||
Porrazzini F,
|
||
Maiella M,
|
||
Ferrari C,
|
||
Caltagirone C,
|
||
Santarnecchi E,
|
||
Bozzali M,
|
||
Martorana A</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2022 Nov 21;145(11):3776-3786.
|
||
doi: 10.1093/brain/awac285.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36281767" target="_blank">36281767</a><a href="/pmc/articles/PMC9679166" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34668959">Sleep and longitudinal cognitive performance in preclinical and early symptomatic Alzheimer's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lucey BP,
|
||
Wisch J,
|
||
Boerwinkle AH,
|
||
Landsness EC,
|
||
Toedebusch CD,
|
||
McLeland JS,
|
||
Butt OH,
|
||
Hassenstab J,
|
||
Morris JC,
|
||
Ances BM,
|
||
Holtzman DM</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2021 Oct 22;144(9):2852-2862.
|
||
doi: 10.1093/brain/awab272.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34668959" target="_blank">34668959</a><a href="/pmc/articles/PMC8536939" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33726524">Sleep Abnormalities in Schizophrenia: State of the Art and Next Steps.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ferrarelli F</span><br />
|
||
<span class="medgenPMjournal">Am J Psychiatry</span>
|
||
2021 Oct 1;178(10):903-913.
|
||
Epub 2021 Mar 17
|
||
doi: 10.1176/appi.ajp.2020.20070968.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33726524" target="_blank">33726524</a><a href="/pmc/articles/PMC8446088" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32090418">European Academy of Neurology guideline on the diagnosis of coma and other disorders of consciousness.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kondziella D,
|
||
Bender A,
|
||
Diserens K,
|
||
van Erp W,
|
||
Estraneo A,
|
||
Formisano R,
|
||
Laureys S,
|
||
Naccache L,
|
||
Ozturk S,
|
||
Rohaut B,
|
||
Sitt JD,
|
||
Stender J,
|
||
Tiainen M,
|
||
Rossetti AO,
|
||
Gosseries O,
|
||
Chatelle C;
|
||
EAN Panel on Coma, Disorders of Consciousness</span><br />
|
||
<span class="medgenPMjournal">Eur J Neurol</span>
|
||
2020 May;27(5):741-756.
|
||
Epub 2020 Feb 23
|
||
doi: 10.1111/ene.14151.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32090418" target="_blank">32090418</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/1884339">Sleep disturbance in depression reconsidered.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Southmayd SE,
|
||
Cairns J,
|
||
David MM</span><br />
|
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<span class="medgenPMjournal">Can J Psychiatry</span>
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1991 Jun;36(5):366-73.
|
||
doi: 10.1177/070674379103600510.
|
||
<span class="bold">PMID: </span><a href="/pubmed/1884339" target="_blank">1884339</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22EEG%20with%20generalized%20slow%20activity%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 (400)</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/38976954">A systematic review of electroencephalographic findings in Lennox-Gastaut syndrome.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nizami FM,
|
||
Trivedi S,
|
||
Kalita J</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Res</span>
|
||
2024 Sep;205:107406.
|
||
Epub 2024 Jul 2
|
||
doi: 10.1016/j.eplepsyres.2024.107406.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38976954" target="_blank">38976954</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35482160">Acute stroke-like deficits associated with nonketotic hyperglycemic hyperosmolar state: an illustrative case and systematic review of literature.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rossi S,
|
||
Romoli M,
|
||
Urbinati G,
|
||
Benini M,
|
||
Russo M,
|
||
D'Anna L,
|
||
Abu-Rumeileh S,
|
||
Sacco S,
|
||
Querzani P,
|
||
Foschi M</span><br />
|
||
<span class="medgenPMjournal">Neurol Sci</span>
|
||
2022 Aug;43(8):4671-4683.
|
||
Epub 2022 Apr 28
|
||
doi: 10.1007/s10072-022-06088-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35482160" target="_blank">35482160</a><a href="/pmc/articles/PMC9349111" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35131107">Medical treatment of Rasmussen's Encephalitis: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lagarde S,
|
||
Boucraut J,
|
||
Bartolomei F</span><br />
|
||
<span class="medgenPMjournal">Rev Neurol (Paris)</span>
|
||
2022 Sep;178(7):675-691.
|
||
Epub 2022 Feb 4
|
||
doi: 10.1016/j.neurol.2022.01.007.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35131107" target="_blank">35131107</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32971385">Electroencephalographic findings in antileucine-rich glioma-inactivated 1 (LGI1) autoimmune encephalitis: A systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Roberto KT,
|
||
Espiritu AI,
|
||
Fernandez MLL,
|
||
Gutierrez JC</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Behav</span>
|
||
2020 Nov;112:107462.
|
||
Epub 2020 Sep 22
|
||
doi: 10.1016/j.yebeh.2020.107462.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32971385" target="_blank">32971385</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26899133">Coffee, caffeine, and sleep: A systematic review of epidemiological studies and randomized controlled trials.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Clark I,
|
||
Landolt HP</span><br />
|
||
<span class="medgenPMjournal">Sleep Med Rev</span>
|
||
2017 Feb;31:70-78.
|
||
Epub 2016 Jan 30
|
||
doi: 10.1016/j.smrv.2016.01.006.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26899133" target="_blank">26899133</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22EEG%20with%20generalized%20slow%20activity%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 (6)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
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|
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|
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|
||
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|
||
|
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|
||
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|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
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||
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|
||
|
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<div class="portlet mgSection" id="ID_113">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Table_of_contents">Table of contents</h1><a sid="113" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Clinical_resources">Clinical resources</h1><a sid="119" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul><li><a href="https://clinicaltrials.gov/search?cond=EEG%20with%20generalized%20slow%20activity" 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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