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<meta name="keywords" content="C4024965, anatomical abnormality, frontal cortex degeneration, frontal cortical atrophy, 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="Atrophy of the frontal cortex." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=870517
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ConceptID=C4024965
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Frontal cortical atrophy</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>870517</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:">C4024965</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Anatomical Abnormality</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Frontal cortex degeneration</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>HPO:</td>
|
||
<td><a target="_blank" title="Human Phenotype Ontology" href="https://hpo.jax.org/app/browse/term/HP:0006913">HP:0006913</a></td></tr>
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Definition">Definition</h1><a sid="100" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">Atrophy of the frontal cortex. [from <a title="Human Phenotype Ontology" href="http://www.human-phenotype-ontology.org" class="defSource" target="_blank">HPO</a>]</div>
|
||
</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">Frontal cortical atrophy</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/892343" ref="tree=MeSH" title="MedGen record for Morphological central nervous system abnormality">Morphological central nervous system abnormality</a></span><ul><li><span class="TLline"><a href="/medgen/866738" ref="tree=MeSH" title="MedGen record for Abnormal brain morphology">Abnormal brain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/866620" ref="tree=MeSH" title="MedGen record for Abnormal forebrain morphology">Abnormal forebrain morphology</a></span><ul><li><span class="TLline"><a href="/medgen/867394" ref="tree=MeSH" title="MedGen record for Abnormal cerebral morphology">Abnormal cerebral morphology</a></span><ul><li><span class="TLline"><a href="/medgen/871221" ref="tree=MeSH" title="MedGen record for Abnormal cerebral cortex morphology">Abnormal cerebral cortex morphology</a></span><ul><li><span class="TLline"><a href="/medgen/1646740" ref="tree=MeSH" title="MedGen record for Cerebral cortical atrophy">Cerebral cortical atrophy</a></span><ul><li><span class="matched_ds">Frontal cortical atrophy</span></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></li></ul></div></div></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_112">
|
||
<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_347622"><div><strong>Huntington disease-like 3</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>347622</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.">C1858114</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on brain MRI) progressive frontal cortical atrophy and bilateral caudate atrophy.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/347622">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_437111"><div><strong>Syndromic X-linked intellectual disability 94</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>437111</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.">C2678051</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has material basis in mutation in the GRIA3 gene on chromosome Xq25.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/437111">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_934738"><div><strong>Intellectual disability, autosomal dominant 43</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>934738</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.">C4310771</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div></div>
|
||
<div class="spaceAbove">HIVEP2-related intellectual disability is a neurological disorder characterized by moderate to severe developmental delay and intellectual disability and mild physical abnormalities (dysmorphic features). Early symptoms of the condition include weak muscle tone (hypotonia) and delayed development of motor skills, such as sitting, standing, and walking. After learning to walk, many affected individuals continue to have difficulty with this activity; their walking style (gait) is often unbalanced and wide-based. Speech is also delayed, and some people with this condition never learn to talk. Most people with HIVEP2-related intellectual disability also have unusual physical features, such as widely spaced eyes (hypertelorism), a broad nasal bridge, or fingers with tapered ends, although there is no characteristic pattern of such features among affected individuals. Many people with the condition exhibit neurodevelopmental disorders, such as hyperactivity, attention deficit disorder, aggression, anxiety, and autism spectrum disorder, which is a group of developmental disorders characterized by impaired communication and social interaction.\n\nOther features of HIVEP2-related intellectual disability include mild abnormalities in the structure of the brain and an abnormally small brain and head size (microcephaly). Less common health problems include seizures; recurrent ear infections; and eye disorders, such as eyes that do not look in the same direction (strabismus), "lazy eye" (amblyopia), and farsightedness (hyperopia). Some people with HIVEP2-related intellectual disability have gastrointestinal problems, which can include backflow of acidic stomach contents into the esophagus (gastroesophageal reflux) and constipation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/934738">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1641069"><div><strong>Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1641069</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.">C4551951</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Inclusion body myopathy associated with Paget disease of bone (PDB) and/or frontotemporal dementia (IBMPFD) is characterized by adult-onset proximal and distal muscle weakness (clinically resembling a limb-girdle muscular dystrophy syndrome), early-onset PDB, and premature frontotemporal dementia (FTD). Muscle weakness progresses to involve other limb and respiratory muscles. PDB involves focal areas of increased bone turnover that typically lead to spine and/or hip pain and localized enlargement and deformity of the long bones; pathologic fractures occur on occasion. Early stages of FTD are characterized by dysnomia, dyscalculia, comprehension deficits, and paraphasic errors, with minimal impairment of episodic memory; later stages are characterized by inability to speak, auditory comprehension deficits for even one-step commands, alexia, and agraphia. Mean age at diagnosis for muscle disease and PDB is 42 years; for FTD, 56 years. Dilated cardiomyopathy, amyotrophic lateral sclerosis, and Parkinson disease are now known to be part of the spectrum of findings associated with IBMPFD.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1641069">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684253"><div><strong>Developmental and epileptic encephalopathy, 75</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684253</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.">C5193099</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Developmental and epileptic encephalopathy-75 (DEE75) is an autosomal recessive neurodevelopmental and neurodegenerative disorder characterized by onset of severe refractory seizures in the first months of life. Patients often have global developmental delay before the onset of seizures, and thereafter achieve few milestones. EEG usually shows multifocal spikes and hypsarrhythmia, consistent with a clinical diagnosis of West syndrome. They have severely impaired intellectual development with inability to walk, absent speech, and hypotonia with axial hyperreflexia. Brain imaging shows progressive cerebral atrophy, frontal lobe atrophy, white matter abnormalities, and delayed myelination. Since the disorder is due to mitochondrial dysfunction, some patients may develop other organ involvement, including cardiomyopathy or liver and renal dysfunction. Death may occur in childhood (summary by Yin et al., 2018). For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684253">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1684706"><div><strong>Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1684706</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.">C5231494</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Neurogenic arthrogryposis multiplex congenita-4 with agenesis of the corpus callosum (AMC4) is a severe neurologic disorder with onset in utero. Affected individuals show little or no fetal movements and are born with significant contractures affecting the upper and lower limbs, as well as dysmorphic facial features. Other abnormalities include globally impaired development, optic atrophy, agenesis of the corpus callosum, seizures, and peripheral neuropathy. Many patients die in early childhood (summary by Seidahmed et al., 2020).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1684706">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684706" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1684253" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Developmental and epileptic encephalopathy, 75</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_347622" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Huntington disease-like 3</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1641069" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_934738" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Intellectual disability, autosomal dominant 43</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_437111" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Syndromic X-linked intellectual disability 94</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/24838911">APOE genotype and neuroimaging markers of Alzheimer's disease: systematic review and meta-analysis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Liu Y,
|
||
Yu JT,
|
||
Wang HF,
|
||
Han PR,
|
||
Tan CC,
|
||
Wang C,
|
||
Meng XF,
|
||
Risacher SL,
|
||
Saykin AJ,
|
||
Tan L</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2015 Feb;86(2):127-34.
|
||
Epub 2014 May 16
|
||
doi: 10.1136/jnnp-2014-307719.
|
||
<span class="bold">PMID: </span><a href="/pubmed/24838911" target="_blank">24838911</a><a href="/pmc/articles/PMC4331076" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/11310619">Primary progressive aphasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mesulam MM</span><br />
|
||
<span class="medgenPMjournal">Ann Neurol</span>
|
||
2001 Apr;49(4):425-32.
|
||
<span class="bold">PMID: </span><a href="/pubmed/11310619" target="_blank">11310619</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8163988">Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
1994 Apr;57(4):416-8.
|
||
doi: 10.1136/jnnp.57.4.416.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8163988" target="_blank">8163988</a><a href="/pmc/articles/PMC1072868" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(frontal%20cortical%20atrophy)%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 (38)</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/28600444">Deconstructing psychosis and misperception symptoms in Parkinson's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Nishio Y,
|
||
Yokoi K,
|
||
Uchiyama M,
|
||
Mamiya Y,
|
||
Watanabe H,
|
||
Gang M,
|
||
Baba T,
|
||
Takeda A,
|
||
Hirayama K,
|
||
Mori E</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2017 Sep;88(9):722-729.
|
||
Epub 2017 Jun 9
|
||
doi: 10.1136/jnnp-2017-315741.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28600444" target="_blank">28600444</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28486594">Apathy and impulsivity in frontotemporal lobar degeneration syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lansdall CJ,
|
||
Coyle-Gilchrist ITS,
|
||
Jones PS,
|
||
Vázquez Rodríguez P,
|
||
Wilcox A,
|
||
Wehmann E,
|
||
Dick KM,
|
||
Robbins TW,
|
||
Rowe JB</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2017 Jun 1;140(6):1792-1807.
|
||
doi: 10.1093/brain/awx101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28486594" target="_blank">28486594</a><a href="/pmc/articles/PMC5868210" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27056065">Frontal Cortical Atrophy as a Predictor of Poststroke Apathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mihalov J,
|
||
Mikula P,
|
||
Budiš J,
|
||
Valkovič P</span><br />
|
||
<span class="medgenPMjournal">J Geriatr Psychiatry Neurol</span>
|
||
2016 Jul;29(4):171-6.
|
||
Epub 2016 Apr 6
|
||
doi: 10.1177/0891988716641248.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27056065" target="_blank">27056065</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20826875">Cortical and frontal atrophy are associated with cognitive impairment in age-related confluent white-matter lesion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mok V,
|
||
Wong KK,
|
||
Xiong Y,
|
||
Wong A,
|
||
Schmidt R,
|
||
Chu W,
|
||
Hu X,
|
||
Leung EY,
|
||
Chen S,
|
||
Chen Y,
|
||
Tang WK,
|
||
Chen X,
|
||
Ho CL,
|
||
Wong KS,
|
||
Wong ST</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2011 Jan;82(1):52-7.
|
||
Epub 2010 Sep 8
|
||
doi: 10.1136/jnnp.2009.201665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20826875" target="_blank">20826875</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20598216">Problem-solving abilities and frontal lobe cortical thickness in healthy aging and mild cognitive impairment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sánchez-Benavides G,
|
||
Gómez-Ansón B,
|
||
Quintana M,
|
||
Vives Y,
|
||
Manero RM,
|
||
Sainz A,
|
||
Blesa R,
|
||
Molinuevo JL,
|
||
Peña-Casanova J</span><br />
|
||
<span class="medgenPMjournal">J Int Neuropsychol Soc</span>
|
||
2010 Sep;16(5):836-45.
|
||
Epub 2010 Jul 5
|
||
doi: 10.1017/S135561771000069X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20598216" target="_blank">20598216</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Frontal%20cortical%20atrophy%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 (19)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28486594">Apathy and impulsivity in frontotemporal lobar degeneration syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lansdall CJ,
|
||
Coyle-Gilchrist ITS,
|
||
Jones PS,
|
||
Vázquez Rodríguez P,
|
||
Wilcox A,
|
||
Wehmann E,
|
||
Dick KM,
|
||
Robbins TW,
|
||
Rowe JB</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2017 Jun 1;140(6):1792-1807.
|
||
doi: 10.1093/brain/awx101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28486594" target="_blank">28486594</a><a href="/pmc/articles/PMC5868210" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20826875">Cortical and frontal atrophy are associated with cognitive impairment in age-related confluent white-matter lesion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mok V,
|
||
Wong KK,
|
||
Xiong Y,
|
||
Wong A,
|
||
Schmidt R,
|
||
Chu W,
|
||
Hu X,
|
||
Leung EY,
|
||
Chen S,
|
||
Chen Y,
|
||
Tang WK,
|
||
Chen X,
|
||
Ho CL,
|
||
Wong KS,
|
||
Wong ST</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2011 Jan;82(1):52-7.
|
||
Epub 2010 Sep 8
|
||
doi: 10.1136/jnnp.2009.201665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20826875" target="_blank">20826875</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16638121">Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grosskreutz J,
|
||
Kaufmann J,
|
||
Frädrich J,
|
||
Dengler R,
|
||
Heinze HJ,
|
||
Peschel T</span><br />
|
||
<span class="medgenPMjournal">BMC Neurol</span>
|
||
2006 Apr 25;6:17.
|
||
doi: 10.1186/1471-2377-6-17.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16638121" target="_blank">16638121</a><a href="/pmc/articles/PMC1459868" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/12682334">Progressive affective aprosodia and prosoplegia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Ghacibeh GA,
|
||
Heilman KM</span><br />
|
||
<span class="medgenPMjournal">Neurology</span>
|
||
2003 Apr 8;60(7):1192-4.
|
||
doi: 10.1212/01.wnl.0000055870.48864.87.
|
||
<span class="bold">PMID: </span><a href="/pubmed/12682334" target="_blank">12682334</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/9144110">Frontal cortical atrophy and negative symptoms in patients with chronic alcohol dependence.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Rosse RB,
|
||
Riggs RL,
|
||
Dietrich AM,
|
||
Schwartz BL,
|
||
Deutsch SI</span><br />
|
||
<span class="medgenPMjournal">J Neuropsychiatry Clin Neurosci</span>
|
||
1997 Spring;9(2):280-2.
|
||
doi: 10.1176/jnp.9.2.280.
|
||
<span class="bold">PMID: </span><a href="/pubmed/9144110" target="_blank">9144110</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Frontal%20cortical%20atrophy%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 (17)</a></div><h3 class="subhead">Therapy</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/28486594">Apathy and impulsivity in frontotemporal lobar degeneration syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lansdall CJ,
|
||
Coyle-Gilchrist ITS,
|
||
Jones PS,
|
||
Vázquez Rodríguez P,
|
||
Wilcox A,
|
||
Wehmann E,
|
||
Dick KM,
|
||
Robbins TW,
|
||
Rowe JB</span><br />
|
||
<span class="medgenPMjournal">Brain</span>
|
||
2017 Jun 1;140(6):1792-1807.
|
||
doi: 10.1093/brain/awx101.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28486594" target="_blank">28486594</a><a href="/pmc/articles/PMC5868210" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20826875">Cortical and frontal atrophy are associated with cognitive impairment in age-related confluent white-matter lesion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mok V,
|
||
Wong KK,
|
||
Xiong Y,
|
||
Wong A,
|
||
Schmidt R,
|
||
Chu W,
|
||
Hu X,
|
||
Leung EY,
|
||
Chen S,
|
||
Chen Y,
|
||
Tang WK,
|
||
Chen X,
|
||
Ho CL,
|
||
Wong KS,
|
||
Wong ST</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2011 Jan;82(1):52-7.
|
||
Epub 2010 Sep 8
|
||
doi: 10.1136/jnnp.2009.201665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20826875" target="_blank">20826875</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/8994103">Slowly progressive anarthria with late anterior opercular syndrome: a variant form of frontal cortical atrophy syndromes.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Broussolle E,
|
||
Bakchine S,
|
||
Tommasi M,
|
||
Laurent B,
|
||
Bazin B,
|
||
Cinotti L,
|
||
Cohen L,
|
||
Chazot G</span><br />
|
||
<span class="medgenPMjournal">J Neurol Sci</span>
|
||
1996 Dec;144(1-2):44-58.
|
||
doi: 10.1016/s0022-510x(96)00096-2.
|
||
<span class="bold">PMID: </span><a href="/pubmed/8994103" target="_blank">8994103</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/3965037">Structure and function: brain electrical activity mapping and computed tomography in schizophrenia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Morihisa JM,
|
||
McAnulty GB</span><br />
|
||
<span class="medgenPMjournal">Biol Psychiatry</span>
|
||
1985 Jan;20(1):3-19.
|
||
doi: 10.1016/0006-3223(85)90131-3.
|
||
<span class="bold">PMID: </span><a href="/pubmed/3965037" target="_blank">3965037</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Frontal%20cortical%20atrophy%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 (4)</a></div><h3 class="subhead">Prognosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35064438">Associations between Cortical Thickness and Metamemory in Alzheimer's Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duran T,
|
||
Woo E,
|
||
Otero D,
|
||
Risacher SL,
|
||
Stage E,
|
||
Sanjay AB,
|
||
Nho K,
|
||
West JD,
|
||
Phillips ML,
|
||
Goukasian N,
|
||
Hwang KS,
|
||
Apostolova LG</span><br />
|
||
<span class="medgenPMjournal">Brain Imaging Behav</span>
|
||
2022 Aug;16(4):1495-1503.
|
||
Epub 2022 Jan 22
|
||
doi: 10.1007/s11682-021-00627-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35064438" target="_blank">35064438</a><a href="/pmc/articles/PMC9450553" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28955085">Menkes disease: A rare disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Jafri SK,
|
||
Kumar R,
|
||
Lashari SK,
|
||
Chand P</span><br />
|
||
<span class="medgenPMjournal">J Pak Med Assoc</span>
|
||
2017 Oct;67(10):1609-1611.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28955085" target="_blank">28955085</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27056065">Frontal Cortical Atrophy as a Predictor of Poststroke Apathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mihalov J,
|
||
Mikula P,
|
||
Budiš J,
|
||
Valkovič P</span><br />
|
||
<span class="medgenPMjournal">J Geriatr Psychiatry Neurol</span>
|
||
2016 Jul;29(4):171-6.
|
||
Epub 2016 Apr 6
|
||
doi: 10.1177/0891988716641248.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27056065" target="_blank">27056065</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20826875">Cortical and frontal atrophy are associated with cognitive impairment in age-related confluent white-matter lesion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mok V,
|
||
Wong KK,
|
||
Xiong Y,
|
||
Wong A,
|
||
Schmidt R,
|
||
Chu W,
|
||
Hu X,
|
||
Leung EY,
|
||
Chen S,
|
||
Chen Y,
|
||
Tang WK,
|
||
Chen X,
|
||
Ho CL,
|
||
Wong KS,
|
||
Wong ST</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2011 Jan;82(1):52-7.
|
||
Epub 2010 Sep 8
|
||
doi: 10.1136/jnnp.2009.201665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20826875" target="_blank">20826875</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16638121">Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Grosskreutz J,
|
||
Kaufmann J,
|
||
Frädrich J,
|
||
Dengler R,
|
||
Heinze HJ,
|
||
Peschel T</span><br />
|
||
<span class="medgenPMjournal">BMC Neurol</span>
|
||
2006 Apr 25;6:17.
|
||
doi: 10.1186/1471-2377-6-17.
|
||
<span class="bold">PMID: </span><a href="/pubmed/16638121" target="_blank">16638121</a><a href="/pmc/articles/PMC1459868" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Frontal%20cortical%20atrophy%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 (11)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/35064438">Associations between Cortical Thickness and Metamemory in Alzheimer's Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Duran T,
|
||
Woo E,
|
||
Otero D,
|
||
Risacher SL,
|
||
Stage E,
|
||
Sanjay AB,
|
||
Nho K,
|
||
West JD,
|
||
Phillips ML,
|
||
Goukasian N,
|
||
Hwang KS,
|
||
Apostolova LG</span><br />
|
||
<span class="medgenPMjournal">Brain Imaging Behav</span>
|
||
2022 Aug;16(4):1495-1503.
|
||
Epub 2022 Jan 22
|
||
doi: 10.1007/s11682-021-00627-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35064438" target="_blank">35064438</a><a href="/pmc/articles/PMC9450553" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27094093">Patterns of cortical thinning in nondemented Parkinson's disease patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Uribe C,
|
||
Segura B,
|
||
Baggio HC,
|
||
Abos A,
|
||
Marti MJ,
|
||
Valldeoriola F,
|
||
Compta Y,
|
||
Bargallo N,
|
||
Junque C</span><br />
|
||
<span class="medgenPMjournal">Mov Disord</span>
|
||
2016 May;31(5):699-708.
|
||
Epub 2016 Apr 20
|
||
doi: 10.1002/mds.26590.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27094093" target="_blank">27094093</a><a href="/pmc/articles/PMC5061099" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27056065">Frontal Cortical Atrophy as a Predictor of Poststroke Apathy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mihalov J,
|
||
Mikula P,
|
||
Budiš J,
|
||
Valkovič P</span><br />
|
||
<span class="medgenPMjournal">J Geriatr Psychiatry Neurol</span>
|
||
2016 Jul;29(4):171-6.
|
||
Epub 2016 Apr 6
|
||
doi: 10.1177/0891988716641248.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27056065" target="_blank">27056065</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20826875">Cortical and frontal atrophy are associated with cognitive impairment in age-related confluent white-matter lesion.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Mok V,
|
||
Wong KK,
|
||
Xiong Y,
|
||
Wong A,
|
||
Schmidt R,
|
||
Chu W,
|
||
Hu X,
|
||
Leung EY,
|
||
Chen S,
|
||
Chen Y,
|
||
Tang WK,
|
||
Chen X,
|
||
Ho CL,
|
||
Wong KS,
|
||
Wong ST</span><br />
|
||
<span class="medgenPMjournal">J Neurol Neurosurg Psychiatry</span>
|
||
2011 Jan;82(1):52-7.
|
||
Epub 2010 Sep 8
|
||
doi: 10.1136/jnnp.2009.201665.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20826875" target="_blank">20826875</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/20598216">Problem-solving abilities and frontal lobe cortical thickness in healthy aging and mild cognitive impairment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Sánchez-Benavides G,
|
||
Gómez-Ansón B,
|
||
Quintana M,
|
||
Vives Y,
|
||
Manero RM,
|
||
Sainz A,
|
||
Blesa R,
|
||
Molinuevo JL,
|
||
Peña-Casanova J</span><br />
|
||
<span class="medgenPMjournal">J Int Neuropsychol Soc</span>
|
||
2010 Sep;16(5):836-45.
|
||
Epub 2010 Jul 5
|
||
doi: 10.1017/S135561771000069X.
|
||
<span class="bold">PMID: </span><a href="/pubmed/20598216" target="_blank">20598216</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Frontal%20cortical%20atrophy%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 (13)</a></div></div>
|
||
</div>
|
||
</div></div></div></div></div></div></div>
|
||
<div id="messagearea_bottom">
|
||
|
||
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|
||
<div class=" bottom">
|
||
|
||
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|
||
|
||
</div>
|
||
</div>
|
||
<div class="supplemental col three_col last">
|
||
<h2 class="offscreen_noflow">Supplemental Content</h2>
|
||
|
||
<div>
|
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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=Frontal%20cortical%20atrophy" target="_blank">ClinicalTrials.gov</a></li></ul></div>
|
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Practice_guidelines">Practice guidelines</h1><a sid="121" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln"><ul class="a_poppers"><li><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(frontal%20cortical%20atrophy)%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></ul></div>
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<div class="portlet_content ln"><ul><li><a href="https://vsearch.nlm.nih.gov/vivisimo/cgi-bin/query-meta?v:project=medlineplus&query=Frontal%20cortical%20atrophy" target="_blank">MedlinePlus</a></li></ul></div>
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|
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|
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<a href="/pubmed/clinical?term=Frontal%20cortical%20atrophy" ref="ncbi_uid=&discoId=gtr_reviews&linkpos=1&linkpostotal=2" target="_blank">PubMed Clinical Queries</a>
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<a href="/pubmed?term=Frontal%20cortical%20atrophy%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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<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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Clear
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Turn On
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<a class="htb ralinkpopperctrl" ref="log$=activity&linkpos=1" href="/portal/utils/pageresolver.fcgi?recordid=67ce920bf4a390645e335dea">Frontal cortical atrophy</a>
|
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<div class="ralinkpop offscreen_noflow">Frontal cortical atrophy<div class="brieflinkpopdesc"></div></div>
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<div class="tertiary">MedGen</div>
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