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<meta name="keywords" content="C4544271, impaired executive function, impaired executive functioning, mental or behavioral dysfunction, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="A disturbance of executive functioning, which is broadly defined as the set of abilities that allow for the planning, executing, monitoring, and self-correcting of goal-directed behavior while inhibiting task-irrelevant behavior. At least some degree of executive skill is needed to complete most cognitive tasks, and deficits in executive abilities are central to many clinical conditions, including fronto-temporal dementia." /><meta name="robots" content="index,nofollow,noarchive" />
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<!--
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UID=1617231
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ConceptID=C4544271
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Impaired executive functioning</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1617231</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.">C4544271</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Mental or Behavioral Dysfunction</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Impaired executive function</td></tr>
|
||
<tr><td><span class="bold">SNOMED CT: </span></td>
|
||
<td>Impaired executive functioning (736317001)</td></tr>
|
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<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:0033051">HP:0033051</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>
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<div class="portlet_content ln">A disturbance of executive functioning, which is broadly defined as the set of abilities that allow for the planning, executing, monitoring, and self-correcting of goal-directed behavior while inhibiting task-irrelevant behavior. At least some degree of executive skill is needed to complete most cognitive tasks, and deficits in executive abilities are central to many clinical conditions, including fronto-temporal dementia. [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 class="portlet mgSection" id="ID_118">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Term_Hierarchy">Term Hierarchy</h1><a sid="118" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
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<div class="portlet_content ln HierarchyGTR"><div class="jig-ncbitabs"><ul><li><a href="#tabGTR">GTR</a></li><li><a href="#tabMGEN">MeSH</a></li></ul><div id="tabGTR"><div class="search_result"><div class="rprts"><div class="chiclet_legend"><span class="chiclet_list" style="position:static;"><span title="Clinical test" class="chiclet Ccolor round">C</span><span>Clinical test, </span><span title="Research test" class="chiclet Rcolor round">R</span><span>Research test, </span><span title="OMIM" class="chiclet Ocolor ">O</span><span>OMIM, </span><span title="GeneReview" class="chiclet Gcolor">G</span><span><em>GeneReviews</em>, </span><span title="ClinVar" class="chiclet Vcolor">V</span><span>ClinVar </span></span></div><div id="hierarchy" class="margin_t1"><div class="ds_tree"><ul><li class="matched_ds"><span class="chiclet_list"><span class="chiclet unavailable round" title="Clinical test">C</span><span class="chiclet unavailable round" title="Research Tests">R</span><span class="chiclet unavailable" title="OMIM">O</span><span class="chiclet unavailable" title="GeneReviews">G</span><span class="chiclet unavailable" title="ClinVar">V</span></span><span class="TLline">Impaired executive functioning</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/1254" ref="tree=MeSH" title="MedGen record for Fetal anomaly">Fetal anomaly</a></span><ul><li><span class="TLline"><a href="/medgen/474891" ref="tree=MeSH" title="MedGen record for Congenital Systemic Disorder">Congenital Systemic Disorder</a></span><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/868938" ref="tree=MeSH" title="MedGen record for Abnormality of mental function">Abnormality of mental function</a></span><ul><li><span class="TLline"><a href="/medgen/14048" ref="tree=MeSH" title="MedGen record for Atypical behavior">Atypical behavior</a></span><ul><li><span class="matched_ds">Impaired executive functioning</span><ul><li><span class="TLline"><a href="/medgen/1772134" ref="tree=MeSH" title="MedGen record for Impaired ability to organize">Impaired ability to organize</a></span></li><li><span class="TLline"><a href="/medgen/1727108" ref="tree=MeSH" title="MedGen record for Impaired ability to plan">Impaired ability to plan</a></span></li><li><span class="TLline"><a href="/medgen/1784885" ref="tree=MeSH" title="MedGen record for Impaired ability to shift attention">Impaired ability to shift attention</a></span></li><li><span class="TLline"><a href="/medgen/1777890" ref="tree=MeSH" title="MedGen record for Impaired self monitoring">Impaired self monitoring</a></span></li><li><span class="TLline"><a href="/medgen/1725549" ref="tree=MeSH" title="MedGen record for Impaired task monitoring">Impaired task monitoring</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>
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<div class="portlet_content ln clinfeat">
|
||
<div class="divPopper rprt" id="rdis_335442"><div><strong>Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>335442</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.">C1846492</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">VPS13D movement disorder is a hyperkinetic movement disorder (dystonia, chorea, and/or ataxia) of variable age of onset that can be associated with developmental delay. Onset ranges from birth to adulthood. Individuals can present in childhood with motor delays and gait instability. Cognitive impairment ranging from mild intellectual disability to developmental delay has been reported, and several individuals have normal cognitive function. Individuals have also presented as young adults with gait difficulties caused by spastic ataxia or ataxia. In addition to gait ataxia, affected individuals had limb ataxia, dysarthria, and eye movement abnormalities (macro-saccadic oscillations, nystagmus, and saccadic pursuit). Additional features reported in some individuals include peripheral neuropathy and/or seizures. The disorder progresses to spastic ataxia or generalized dystonia, which can lead to loss of independent ambulation.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/335442">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_339552"><div><strong>Hereditary spastic paraplegia 7</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>339552</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:">C1846564</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spastic paraplegia 7 (SPG7) is characterized by insidiously progressive bilateral leg weakness and spasticity. Most affected individuals have decreased vibration sense and cerebellar signs. Onset is mostly in adulthood, although symptoms may start as early as age 11 years and as late as age 72 years. Additional features including ataxia (gait and limbs), spastic dysarthria, dysphagia, pale optic disks, ataxia, nystagmus, strabismus, ptosis, hearing loss, motor and sensory neuropathy, amyotrophy, scoliosis, pes cavus, and urinary sphincter disturbances may be observed.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/339552">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_338045"><div><strong>Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>338045</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.">C1850406</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">MPV17-related mitochondrial DNA (mtDNA) maintenance defect presents in the vast majority of affected individuals as an early-onset encephalohepatopathic (hepatocerebral) disease that is typically associated with mtDNA depletion, particularly in the liver. A later-onset neuromyopathic disease characterized by myopathy and neuropathy, and associated with multiple mtDNA deletions in muscle, has also rarely been described. MPV17-related mtDNA maintenance defect, encephalohepatopathic form is characterized by: Hepatic manifestations (liver dysfunction that typically progresses to liver failure, cholestasis, hepatomegaly, and steatosis); Neurologic involvement (developmental delay, hypotonia, microcephaly, and motor and sensory peripheral neuropathy); Gastrointestinal manifestations (gastrointestinal dysmotility, feeding difficulties, and failure to thrive); and Metabolic derangements (lactic acidosis and hypoglycemia). Less frequent manifestations include renal tubulopathy, nephrocalcinosis, and hypoparathyroidism. Progressive liver disease often leads to death in infancy or early childhood. Hepatocellular carcinoma has been reported.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/338045">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_395301"><div><strong>Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>395301</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.">C1859598</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Ataxia-oculomotor apraxia syndrome is an early-onset autosomal recessive cerebellar ataxia with peripheral axonal neuropathy, oculomotor apraxia (defined as the limitation of ocular movements on command), and hypoalbuminemia (Moreira et al., 2001). Genetic Heterogeneity of Ataxia-Oculomotor Apraxia See also AOA2 (606002), caused by mutation in the SETX gene (608465) on chromosome 9q34; AOA3 (615217), caused by mutation in the PIK3R5 gene (611317) on chromosome 17p; and AOA4 (616267), caused by mutation in the PNKP gene (605610) on chromosome 19q13.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/395301">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_467404"><div><strong>Chromosome 15q11.2 deletion syndrome</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>467404</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.">C3180937</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">A heterozygous deletion of chromosome 15q11.2 may increase the susceptibility to neuropsychiatric or neurodevelopmental problems, including delayed psychomotor development, speech delay, autism spectrum disorder, attention deficit-hyperactivity disorder, obsessive-compulsive disorder, and possibly seizures (summary by Doornbos et al., 2009 and Burnside et al., 2011). See also chromosome 15q11.2 duplication syndrome (608636).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/467404">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_815975"><div><strong>Basal ganglia calcification, idiopathic, 5</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>815975</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.">C3809645</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Primary familial brain calcification (PFBC) is a neurodegenerative disorder with characteristic calcium deposits in the basal ganglia and other brain areas visualized on neuroimaging. Most affected individuals are in good health during childhood and young adulthood and typically present in the fourth to fifth decade with a gradually progressive movement disorder and neuropsychiatric symptoms. The movement disorder first manifests as clumsiness, fatigability, unsteady gait, slow or slurred speech, dysphagia, involuntary movements, or muscle cramping. Neuropsychiatric symptoms, often the first or most prominent manifestations, range from mild difficulty with concentration and memory to changes in personality and/or behavior, to psychosis and dementia. Seizures of various types occur frequently, some individuals experience chronic headache and vertigo; urinary urgency or incontinence may be present.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/815975">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1728824"><div><strong>Frontotemporal dementia and/or amyotrophic lateral sclerosis 8</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1728824</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.">C5436881</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Frontotemporal dementia and/or amyotrophic lateral sclerosis-8 (FTDALS8) is an autosomal dominant neurodegenerative disorder characterized by adult-onset dementia manifest as memory impairment, executive dysfunction, and behavioral or personality changes. Some patients may develop ALS or parkinsonism. Neuropathologic studies show frontotemporal lobar degeneration (FTLD) with tau (MAPT; 157140)- and TDP43 (605078)-immunoreactive inclusions (summary by Dobson-Stone et al., 2020). For a discussion of genetic heterogeneity of FTDALS, see FTDALS1 (105550).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1728824">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1778818"><div><strong>CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1778818</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.">C5543440</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Cataracts, spastic paraparesis, and speech delay (CSPSD) is an autosomal dominant disorder characterized by spastic paraparesis and bilateral congenital/juvenile cataracts. Speech delay is a common feature (Ferdinandusse et al., 2021).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1778818">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1794139"><div><strong>Leukoencephalopathy, diffuse hereditary, with spheroids 1</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1794139</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.">C5561929</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">The spectrum of CSF1R-related disorder ranges from early-onset disease (age <18 years) to late-onset disease (age =18 years). Early-onset disease is associated with hypotonia, delayed acquisition of developmental milestones, and non-neurologic manifestations (such as skeletal abnormalities); both early- and late-onset disease have similar neurodegenerative involvement. Most affected individuals eventually become bedridden with spasticity, rigidity, and loss of the ability to walk. They lose speech and voluntary movement and appear to be generally unaware of their surroundings. The last stage of disease progresses to a vegetative state with presence of primitive reflexes, such as visual and tactile grasp, mouth-opening reflex, and sucking reflex. Death most commonly results from pneumonia or other infections. About 500 individuals with CSF1R-related disorder have been reported to date.</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1794139">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1824045"><div><strong>Spinocerebellar ataxia 50</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1824045</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.">C5774272</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Spinocerebellar ataxia-50 (SCA50) is an autosomal dominant neurologic disorder characterized by cerebellar ataxia, oculomotor apraxia and other eye movement abnormalities, and cerebellar atrophy on brain imaging. Most patients develop symptoms as adults, although childhood onset has rarely been reported. Additional more variable features may include tremor, dysarthria, dysphagia, and cognitive impairment with executive dysfunction (Coutelier et al., 2022; Schoggl et al., 2022).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1824045">Condition Record</a></div></div>
|
||
<div class="divPopper rprt" id="rdis_1840995"><div><strong>Amyotrophic lateral sclerosis 27, juvenile</strong><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1840995</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.">C5830359</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div></div>
|
||
<div class="spaceAbove">Juvenile amyotrophic lateral sclerosis-27 (ALS27) is an autosomal dominant disorder characterized by early childhood-onset lower extremity spasticity manifesting as toe walking and gait abnormalities, followed by progressive lower motor neuron-mediated weakness without sensory signs or symptoms (Mohassel et al., 2021). For a discussion of genetic heterogeneity of amyotrophic lateral sclerosis, see ALS1 (105400).</div>
|
||
<div class="spaceAbove nowrap">See: <a href="/medgen/1840995">Condition Record</a></div></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1840995" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Amyotrophic lateral sclerosis 27, juvenile</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_395301" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_335442" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_815975" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Basal ganglia calcification, idiopathic, 5</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1778818" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">CATARACTS, SPASTIC PARAPARESIS, AND SPEECH DELAY</a></div><div class="jig-moreless" data-jigconfig="class: 'moveDown', moreText: 'See full list (11)', lessText: 'Show less', nodeBefore: 0"><span id="clinMore">
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_467404" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Chromosome 15q11.2 deletion syndrome</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1728824" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Frontotemporal dementia and/or amyotrophic lateral sclerosis 8</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_339552" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Hereditary spastic paraplegia 7</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1794139" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Leukoencephalopathy, diffuse hereditary, with spheroids 1</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_338045" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Mitochondrial DNA depletion syndrome 6 (hepatocerebral type)</a></div>
|
||
<div class="hangingIndent"><a title="click for more information" class="jig-ncbipopper" href="#rdis_1824045" data-jigconfig="hasArrow: true, openEvent: 'click', closeEvent: 'mouseout', openAnimation: 'fadeIn', closeAnimation: 'fadeOut', triggerPosition: 'center right', destPosition: 'center left', arrowDirection: 'left'">Spinocerebellar ataxia 50</a></div></span></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/33249502">The Cyclical Relation Between Chronic Pain, Executive Functioning, Emotional Regulation, and Self-Management.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Caes L,
|
||
Dick B,
|
||
Duncan C,
|
||
Allan J</span><br />
|
||
<span class="medgenPMjournal">J Pediatr Psychol</span>
|
||
2021 Mar 18;46(3):286-292.
|
||
doi: 10.1093/jpepsy/jsaa114.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33249502" target="_blank">33249502</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22104513">Treatment of adults with attention-deficit/hyperactivity disorder.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Baron DA,
|
||
Pato MT,
|
||
Cyr RL</span><br />
|
||
<span class="medgenPMjournal">J Am Osteopath Assoc</span>
|
||
2011 Nov;111(11):610-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22104513" target="_blank">22104513</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/15249276">Executive functioning, illness course, and relapse/recurrence in continuation and maintenance treatment of late-life depression: is there a relationship?</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Butters MA,
|
||
Bhalla RK,
|
||
Mulsant BH,
|
||
Mazumdar S,
|
||
Houck PR,
|
||
Begley AE,
|
||
Dew MA,
|
||
Pollock BG,
|
||
Nebes RD,
|
||
Becker JT,
|
||
Reynolds CF 3rd</span><br />
|
||
<span class="medgenPMjournal">Am J Geriatr Psychiatry</span>
|
||
2004 Jul-Aug;12(4):387-94.
|
||
doi: 10.1176/appi.ajgp.12.4.387.
|
||
<span class="bold">PMID: </span><a href="/pubmed/15249276" target="_blank">15249276</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(%22impaired%20executive%20functioning%22%5Btiab%3A~0%5D)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (3)</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/38795457">Impaired executive functioning in children of women with epilepsy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Adriaenssen DJ,
|
||
Huuse Farmen A,
|
||
Glenne Øie M,
|
||
Winther Skogli E</span><br />
|
||
<span class="medgenPMjournal">Epilepsy Behav</span>
|
||
2024 Jul;156:109864.
|
||
Epub 2024 May 24
|
||
doi: 10.1016/j.yebeh.2024.109864.
|
||
<span class="bold">PMID: </span><a href="/pubmed/38795457" target="_blank">38795457</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34552015">Short- and Long-Term Complications of Bronchopulmonary Dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Homan TD,
|
||
Nayak RP</span><br />
|
||
<span class="medgenPMjournal">Respir Care</span>
|
||
2021 Oct;66(10):1618-1629.
|
||
doi: 10.4187/respcare.08401.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34552015" target="_blank">34552015</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33092494">Impairments in Executive Functioning in Patients with Comorbid Substance Use and Personality Disorders: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moraleda-Barreno E,
|
||
Cáceres Pachón MDP,
|
||
Lozano ÓM,
|
||
Pérez Moreno PJ,
|
||
Lorca Marín JA,
|
||
Fernández-Calderón F,
|
||
Díaz Batanero C,
|
||
Gómez-Bujedo J</span><br />
|
||
<span class="medgenPMjournal">J Dual Diagn</span>
|
||
2021 Jan-Mar;17(1):64-79.
|
||
Epub 2020 Oct 22
|
||
doi: 10.1080/15504263.2020.1829769.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33092494" target="_blank">33092494</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30382543">Weight and age do not account for a worse executive functioning among BED-obese patients.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Aloi M,
|
||
Rania M,
|
||
de Filippis R,
|
||
Segura-Garcia C</span><br />
|
||
<span class="medgenPMjournal">Eat Weight Disord</span>
|
||
2020 Apr;25(2):373-377.
|
||
Epub 2018 Oct 31
|
||
doi: 10.1007/s40519-018-0608-9.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30382543" target="_blank">30382543</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29143762">Executive Function Capacities, Negative Driving Behavior and Crashes in Young Drivers.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Walshe EA,
|
||
Ward McIntosh C,
|
||
Romer D,
|
||
Winston FK</span><br />
|
||
<span class="medgenPMjournal">Int J Environ Res Public Health</span>
|
||
2017 Oct 28;14(11)
|
||
doi: 10.3390/ijerph14111314.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29143762" target="_blank">29143762</a><a href="/pmc/articles/PMC5707953" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Impaired%20executive%20functioning%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 (85)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/38795457">Impaired executive functioning in children of women with epilepsy.</a></div>
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Huuse Farmen A,
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|
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|
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<span class="bold">PMID: </span><a href="/pubmed/38795457" target="_blank">38795457</a></div>
|
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<div class="nl"><a target="_blank" href="/pubmed/36476065">Impaired executive functioning mediates the association between aging and deterministic sequence learning.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Petok JR,
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Dang L,
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Hammel B</span><br />
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Epub 2022 Dec 7
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<div class="nl"><a target="_blank" href="/pubmed/37530261">Association between severe retinopathy of prematurity (ROP) and poor motor neurodevelopmental outcome.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/33092494">Impairments in Executive Functioning in Patients with Comorbid Substance Use and Personality Disorders: A Systematic Review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Moraleda-Barreno E,
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Cáceres Pachón MDP,
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Lozano ÓM,
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Lorca Marín JA,
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<span class="bold">PMID: </span><a href="/pubmed/33092494" target="_blank">33092494</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/30987935">The effect of type 1 diabetes on the developing brain.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cameron FJ,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Impaired%20executive%20functioning%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 (61)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/38795457">Impaired executive functioning in children of women with epilepsy.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Adriaenssen DJ,
|
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Huuse Farmen A,
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Glenne Øie M,
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Winther Skogli E</span><br />
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<span class="medgenPMjournal">Epilepsy Behav</span>
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2024 Jul;156:109864.
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Epub 2024 May 24
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doi: 10.1016/j.yebeh.2024.109864.
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<span class="bold">PMID: </span><a href="/pubmed/38795457" target="_blank">38795457</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/36190537">The relationship between executive functioning and addictive behavior: new insights from a longitudinal community study.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28755189">Neurological and Neuropsychological Problems in Tyrosinemia Type I Patients.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">van Ginkel WG,
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<div class="nl"><a target="_blank" href="/pubmed/22310036">The role of executive function in posttraumatic stress disorder: a systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Polak AR,
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Witteveen AB,
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Reitsma JB,
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Olff M</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/22310036" target="_blank">22310036</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/22104513">Treatment of adults with attention-deficit/hyperactivity disorder.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Baron DA,
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<span class="medgenPMjournal">J Am Osteopath Assoc</span>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Impaired%20executive%20functioning%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 (19)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/36476065">Impaired executive functioning mediates the association between aging and deterministic sequence learning.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Petok JR,
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Dang L,
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Hammel B</span><br />
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<span class="medgenPMjournal">Neuropsychol Dev Cogn B Aging Neuropsychol Cogn</span>
|
||
2024 Jan-Mar;31(2):323-339.
|
||
Epub 2022 Dec 7
|
||
doi: 10.1080/13825585.2022.2153789.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36476065" target="_blank">36476065</a><a href="/pmc/articles/PMC10244484" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34505554">The association between hyperactive behaviour and cognitive inhibition impairments in young children.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Burley DT,
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Anning KL,
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van Goozen SHM</span><br />
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<span class="medgenPMjournal">Child Neuropsychol</span>
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2022 Apr;28(3):302-317.
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Epub 2021 Sep 10
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<span class="bold">PMID: </span><a href="/pubmed/34505554" target="_blank">34505554</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/26580849">IMPAIRED EXECUTIVE FUNCTIONING IN PEDIATRIC TRICHOTILLOMANIA (HAIR PULLING DISORDER).</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Flessner CA,
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Brennan E,
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<span class="medgenPMjournal">Depress Anxiety</span>
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<div class="nl"><a target="_blank" href="/pubmed/25464067">Impaired executive functioning influences verbal memory in anorexia nervosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Oltra-Cucarella J,
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Rojo Moreno L,
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Arribas Sáiz P,
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Sanguesa García C,
|
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Latorre Paniagua P,
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Hidalgo Muñoz E,
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Rojo Bofill L</span><br />
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2015 Jan;16:47-53.
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Epub 2014 Nov 1
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doi: 10.1016/j.eatbeh.2014.10.013.
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<span class="bold">PMID: </span><a href="/pubmed/25464067" target="_blank">25464067</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/16957489">Verbal fluency predicts mortality in Alzheimer disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Cosentino S,
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Scarmeas N,
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Albert SM,
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Stern Y</span><br />
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<span class="medgenPMjournal">Cogn Behav Neurol</span>
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2006 Sep;19(3):123-9.
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doi: 10.1097/01.wnn.0000213912.87642.3d.
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<span class="bold">PMID: </span><a href="/pubmed/16957489" target="_blank">16957489</a><a href="/pmc/articles/PMC2441850" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Impaired%20executive%20functioning%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 (29)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36476065">Impaired executive functioning mediates the association between aging and deterministic sequence learning.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Petok JR,
|
||
Dang L,
|
||
Hammel B</span><br />
|
||
<span class="medgenPMjournal">Neuropsychol Dev Cogn B Aging Neuropsychol Cogn</span>
|
||
2024 Jan-Mar;31(2):323-339.
|
||
Epub 2022 Dec 7
|
||
doi: 10.1080/13825585.2022.2153789.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36476065" target="_blank">36476065</a><a href="/pmc/articles/PMC10244484" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34552015">Short- and Long-Term Complications of Bronchopulmonary Dysplasia.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Homan TD,
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||
Nayak RP</span><br />
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<span class="medgenPMjournal">Respir Care</span>
|
||
2021 Oct;66(10):1618-1629.
|
||
doi: 10.4187/respcare.08401.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34552015" target="_blank">34552015</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25576650">Acquiring visual information for locomotion by older adults: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Uiga L,
|
||
Cheng KC,
|
||
Wilson MR,
|
||
Masters RS,
|
||
Capio CM</span><br />
|
||
<span class="medgenPMjournal">Ageing Res Rev</span>
|
||
2015 Mar;20:24-34.
|
||
Epub 2015 Jan 7
|
||
doi: 10.1016/j.arr.2014.12.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25576650" target="_blank">25576650</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25464067">Impaired executive functioning influences verbal memory in anorexia nervosa.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Oltra-Cucarella J,
|
||
Rojo Moreno L,
|
||
Arribas Sáiz P,
|
||
Sanguesa García C,
|
||
Latorre Paniagua P,
|
||
Hidalgo Muñoz E,
|
||
Rojo Bofill L</span><br />
|
||
<span class="medgenPMjournal">Eat Behav</span>
|
||
2015 Jan;16:47-53.
|
||
Epub 2014 Nov 1
|
||
doi: 10.1016/j.eatbeh.2014.10.013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25464067" target="_blank">25464067</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22310036">The role of executive function in posttraumatic stress disorder: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Polak AR,
|
||
Witteveen AB,
|
||
Reitsma JB,
|
||
Olff M</span><br />
|
||
<span class="medgenPMjournal">J Affect Disord</span>
|
||
2012 Dec 1;141(1):11-21.
|
||
Epub 2012 Feb 5
|
||
doi: 10.1016/j.jad.2012.01.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22310036" target="_blank">22310036</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Impaired%20executive%20functioning%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 (67)</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/33092494">Impairments in Executive Functioning in Patients with Comorbid Substance Use and Personality Disorders: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Moraleda-Barreno E,
|
||
Cáceres Pachón MDP,
|
||
Lozano ÓM,
|
||
Pérez Moreno PJ,
|
||
Lorca Marín JA,
|
||
Fernández-Calderón F,
|
||
Díaz Batanero C,
|
||
Gómez-Bujedo J</span><br />
|
||
<span class="medgenPMjournal">J Dual Diagn</span>
|
||
2021 Jan-Mar;17(1):64-79.
|
||
Epub 2020 Oct 22
|
||
doi: 10.1080/15504263.2020.1829769.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33092494" target="_blank">33092494</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25576650">Acquiring visual information for locomotion by older adults: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Uiga L,
|
||
Cheng KC,
|
||
Wilson MR,
|
||
Masters RS,
|
||
Capio CM</span><br />
|
||
<span class="medgenPMjournal">Ageing Res Rev</span>
|
||
2015 Mar;20:24-34.
|
||
Epub 2015 Jan 7
|
||
doi: 10.1016/j.arr.2014.12.005.
|
||
<span class="bold">PMID: </span><a href="/pubmed/25576650" target="_blank">25576650</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/22310036">The role of executive function in posttraumatic stress disorder: a systematic review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Polak AR,
|
||
Witteveen AB,
|
||
Reitsma JB,
|
||
Olff M</span><br />
|
||
<span class="medgenPMjournal">J Affect Disord</span>
|
||
2012 Dec 1;141(1):11-21.
|
||
Epub 2012 Feb 5
|
||
doi: 10.1016/j.jad.2012.01.001.
|
||
<span class="bold">PMID: </span><a href="/pubmed/22310036" target="_blank">22310036</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Impaired%20executive%20functioning%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 (3)</a></div></div>
|
||
</div>
|
||
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|
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|
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<h2 class="offscreen_noflow">Supplemental Content</h2>
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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=Impaired%20executive%20functioning" 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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