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<!--
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UID=101195
|
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ConceptID=C0524851
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-->
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<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">Degenerative Disease of Nervous System, Unspecified</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>101195</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.">C0524851</a></dd><dt><span class="dotprefix"> •</span></dt><dd>Disease or Syndrome</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonyms:</td>
|
||
<td>Degenerative Condition, Neurologic; Degenerative Conditions, Neurologic; Degenerative Diseases, Nervous System; Degenerative Diseases, Neurologic; Degenerative Neurologic Disease; Degenerative Neurologic Diseases; Degenerative Neurologic Disorder; Degenerative Neurologic Disorders; Nervous System Degenerative Diseases; Neurodegenerative Disease; Neurodegenerative Diseases; Neurodegenerative Disorder; Neurodegenerative Disorders; Neurologic Degenerative Condition; Neurologic Degenerative Conditions; Neurologic Degenerative Disease; Neurologic Degenerative Diseases; Neurologic Disease, Degenerative; Neurologic Diseases, Degenerative; Neurologic Disorder, Degenerative; Neurologic Disorders, Degenerative</td></tr>
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<div class="portlet_content ln">Evidence of degenerative disease of the nervous system. [from <a title="NCI Thesaurus" href="http://ncit.nci.nih.gov" class="defSource" target="_blank">NCI</a>]</div>
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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">Degenerative Disease of Nervous System, Unspecified</span></li></ul></div></div></div></div></div><div id="tabMGEN"><div class="ds_tree"><ul><li><span class="TLline"><a href="/medgen/21047" ref="tree=MeSH" title="MedGen record for Pathological Conditions, Signs and Symptoms">Pathological Conditions, Signs and Symptoms</a></span><ul><li><span class="TLline"><a href="/medgen/18325" ref="tree=MeSH" title="MedGen record for Pathological process">Pathological process</a></span><ul><li><span class="TLline"><a href="/medgen/4347" ref="tree=MeSH" title="MedGen record for Disease">Disease</a></span><ul><li><span class="TLline"><a href="/medgen/232130" ref="tree=MeSH" title="MedGen record for Disorder by Site">Disorder by Site</a></span><ul><li><span class="TLline"><a href="/medgen/14336" ref="tree=MeSH" title="MedGen record for Disorder of nervous system">Disorder of nervous system</a></span><ul><li><span class="matched_ds">Degenerative Disease of Nervous System, Unspecified</span><ul><li><span class="TLline"><a href="/medgen/906070" ref="tree=MeSH" title="MedGen record for Chronic traumatic encephalopathy">Chronic traumatic encephalopathy</a></span></li><li><span class="TLline"><a href="/medgen/155945" ref="tree=MeSH" title="MedGen record for Heredodegenerative Disorders, Nervous System">Heredodegenerative Disorders, Nervous System</a></span><ul><li><span class="TLline"><a href="/medgen/78724" ref="tree=MeSH" title="MedGen record for Alexander disease">Alexander disease</a></span><ul><li><span class="TLline"><a href="/medgen/1820954" ref="tree=MeSH" title="MedGen record for Alexander disease type I">Alexander disease type I</a></span></li><li><span class="TLline"><a href="/medgen/1842714" ref="tree=MeSH" title="MedGen record for Alexander disease type II">Alexander disease type II</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10158" ref="tree=MeSH" title="MedGen record for Batten-Turner congenital myopathy">Batten-Turner congenital myopathy</a></span><ul><li><span class="TLline"><a href="/medgen/422446" ref="tree=MeSH" title="MedGen record for Congenital myotonia, autosomal dominant form">Congenital myotonia, autosomal dominant form</a></span></li><li><span class="TLline"><a href="/medgen/155852" ref="tree=MeSH" title="MedGen record for Congenital myotonia, autosomal recessive form">Congenital myotonia, autosomal recessive form</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/98277" ref="tree=MeSH" title="MedGen record for Chorea-acanthocytosis">Chorea-acanthocytosis</a></span></li><li><span class="TLline"><a href="/medgen/40363" ref="tree=MeSH" title="MedGen record for Cockayne syndrome">Cockayne syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/155488" ref="tree=MeSH" title="MedGen record 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class="TLline"><a href="/medgen/45207" ref="tree=MeSH" title="MedGen record for Hereditary optic atrophy">Hereditary optic atrophy</a></span><ul><li><span class="TLline"><a href="/medgen/137902" ref="tree=MeSH" title="MedGen record for Autosomal dominant optic atrophy classic form">Autosomal dominant optic atrophy classic form</a></span></li><li><span class="TLline"><a href="/medgen/1647918" ref="tree=MeSH" title="MedGen record for Dominant hereditary optic atrophy">Dominant hereditary optic atrophy</a></span></li><li><span class="TLline"><a href="/medgen/182973" ref="tree=MeSH" title="MedGen record for Leber optic atrophy">Leber optic atrophy</a></span></li><li><span class="TLline"><a href="/medgen/21923" ref="tree=MeSH" title="MedGen record for Wolfram syndrome">Wolfram syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/14355" ref="tree=MeSH" title="MedGen record for Hereditary sensory and autonomic neuropathy">Hereditary sensory and autonomic neuropathy</a></span><ul><li><span class="TLline"><a href="/medgen/1830087" ref="tree=MeSH" title="MedGen record for Congenital insensitivity to pain with hyperhidrosis">Congenital insensitivity to pain with hyperhidrosis</a></span></li><li><span class="TLline"><a href="/medgen/41678" ref="tree=MeSH" title="MedGen record for Familial dysautonomia">Familial dysautonomia</a></span></li><li><span class="TLline"><a href="/medgen/930069" ref="tree=MeSH" title="MedGen record for X-linked hereditary sensory and autonomic neuropathy with hearing loss">X-linked hereditary sensory and autonomic neuropathy with hearing loss</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/5654" ref="tree=MeSH" title="MedGen record for Huntington disease">Huntington disease</a></span><ul><li><span class="TLline"><a href="/medgen/155518" ref="tree=MeSH" title="MedGen record for Juvenile Huntington disease">Juvenile Huntington disease</a></span></li><li><span class="TLline"><a href="/medgen/224821" ref="tree=MeSH" title="MedGen record for Westphal disease">Westphal disease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/333282" ref="tree=MeSH" title="MedGen record for Kennedy disease">Kennedy disease</a></span></li><li><span class="TLline"><a href="/medgen/155631" ref="tree=MeSH" title="MedGen record for Lafora disease">Lafora disease</a></span><ul><li><span class="TLline"><a href="/medgen/1844054" ref="tree=MeSH" title="MedGen record for Myoclonic epilepsy of Lafora 1">Myoclonic epilepsy of Lafora 1</a></span></li><li><span class="TLline"><a href="/medgen/340621" ref="tree=MeSH" title="MedGen record for Myoclonic epilepsy of Lafora 2">Myoclonic epilepsy of Lafora 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10239" ref="tree=MeSH" title="MedGen record for Myotonic dystrophy">Myotonic dystrophy</a></span><ul><li><span class="TLline"><a href="/medgen/98051" ref="tree=MeSH" title="MedGen record for Congenital myotonic dystrophy">Congenital myotonic dystrophy</a></span></li><li><span class="TLline"><a href="/medgen/44565" ref="tree=MeSH" title="MedGen record for Myotonic cataract">Myotonic cataract</a></span></li><li><span class="TLline"><a href="/medgen/419137" ref="tree=MeSH" title="MedGen record for Myotonic dystrophy type 2">Myotonic dystrophy type 2</a></span></li><li><span class="TLline"><a href="/medgen/886881" ref="tree=MeSH" title="MedGen record for Steinert myotonic dystrophy syndrome">Steinert myotonic dystrophy syndrome</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/58149" ref="tree=MeSH" title="MedGen record for Neurofibromatosis">Neurofibromatosis</a></span><ul><li><span class="TLline"><a href="/medgen/68621" ref="tree=MeSH" title="MedGen record for Aggravated Neurofibromatosis">Aggravated Neurofibromatosis</a></span></li><li><span class="TLline"><a href="/medgen/18013" ref="tree=MeSH" title="MedGen record for Neurofibromatosis, type 1">Neurofibromatosis, type 1</a></span></li><li><span class="TLline"><a href="/medgen/18014" ref="tree=MeSH" title="MedGen record for Neurofibromatosis, type 2">Neurofibromatosis, type 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10326" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis">Neuronal ceroid lipofuscinosis</a></span><ul><li><span class="TLline"><a href="/medgen/7230" ref="tree=MeSH" title="MedGen record for Adult neuronal ceroid lipofuscinosis">Adult neuronal ceroid lipofuscinosis</a></span></li><li><span class="TLline"><a href="/medgen/320287" ref="tree=MeSH" title="MedGen record for Ceroid lipofuscinosis, neuronal, 4 (Kufs type)">Ceroid lipofuscinosis, neuronal, 4 (Kufs type)</a></span></li><li><span class="TLline"><a href="/medgen/1790423" ref="tree=MeSH" title="MedGen record for Ceroid lipofuscinosis, neuronal, 6A">Ceroid lipofuscinosis, neuronal, 6A</a></span></li><li><span class="TLline"><a href="/medgen/351189" ref="tree=MeSH" title="MedGen record for Congenital neuronal ceroid lipofuscinosis">Congenital neuronal ceroid lipofuscinosis</a></span></li><li><span class="TLline"><a href="/medgen/75666" ref="tree=MeSH" title="MedGen record for Infantile neuronal ceroid lipofuscinosis">Infantile neuronal ceroid lipofuscinosis</a></span></li><li><span class="TLline"><a href="/medgen/978346" ref="tree=MeSH" title="MedGen record for Juvenile neuronal ceroid lipofuscinosis">Juvenile neuronal ceroid lipofuscinosis</a></span></li><li><span class="TLline"><a href="/medgen/9589" ref="tree=MeSH" title="MedGen record for Late-infantile neuronal ceroid lipofuscinosis">Late-infantile neuronal ceroid lipofuscinosis</a></span></li><li><span class="TLline"><a href="/medgen/340540" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 1">Neuronal ceroid lipofuscinosis 1</a></span></li><li><span class="TLline"><a href="/medgen/155549" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 3">Neuronal ceroid lipofuscinosis 3</a></span></li><li><span class="TLline"><a href="/medgen/376792" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 5">Neuronal ceroid lipofuscinosis 5</a></span></li><li><span class="TLline"><a href="/medgen/325457" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 7">Neuronal ceroid lipofuscinosis 7</a></span></li><li><span class="TLline"><a href="/medgen/332304" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 9">Neuronal ceroid lipofuscinosis 9</a></span></li><li><span class="TLline"><a href="/medgen/350481" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 10">Neuronal ceroid lipofuscinosis 10</a></span></li><li><span class="TLline"><a href="/medgen/355328" ref="tree=MeSH" title="MedGen record for Neuronal ceroid lipofuscinosis 8 northern epilepsy variant">Neuronal ceroid lipofuscinosis 8 northern epilepsy variant</a></span></li><li><span class="TLline"><a href="/medgen/924712" ref="tree=MeSH" title="MedGen record for Neuronal Ceroid Lipofuscinosis Type 4B">Neuronal Ceroid Lipofuscinosis Type 4B</a></span></li><li><span class="TLline"><a href="/medgen/830971" ref="tree=MeSH" title="MedGen record for Parkinsonism due to ATP13A2 deficiency">Parkinsonism due to ATP13A2 deficiency</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/6708" ref="tree=MeSH" title="MedGen record for Pigmentary pallidal degeneration">Pigmentary pallidal degeneration</a></span><ul><li><span class="TLline"><a href="/medgen/1800044" ref="tree=MeSH" title="MedGen record for Atypical pantothenate kinase-associated neurodegeneration">Atypical pantothenate kinase-associated neurodegeneration</a></span></li><li><span class="TLline"><a href="/medgen/1826057" ref="tree=MeSH" title="MedGen record for Classic pantothenate kinase-associated neurodegeneration">Classic pantothenate kinase-associated neurodegeneration</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/148615" ref="tree=MeSH" title="MedGen record for Spinal Muscular Atrophy of Childhood">Spinal Muscular Atrophy of Childhood</a></span></li><li><span class="TLline"><a href="/medgen/11554" ref="tree=MeSH" title="MedGen record for spinocerebellar disease">spinocerebellar disease</a></span><ul><li><span class="TLline"><a href="/medgen/2956" ref="tree=MeSH" title="MedGen record for Early onset cerebellar ataxia with myoclonus">Early onset cerebellar ataxia with myoclonus</a></span></li><li><span class="TLline"><a href="/medgen/5276" ref="tree=MeSH" title="MedGen record for Friedreich ataxia">Friedreich ataxia</a></span></li><li><span class="TLline"><a href="/medgen/10435" ref="tree=MeSH" title="MedGen record for Olivopontocerebellar atrophy">Olivopontocerebellar atrophy</a></span></li><li><span class="TLline"><a href="/medgen/39733" ref="tree=MeSH" title="MedGen record for Spinocerebellar atrophy">Spinocerebellar atrophy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/3941" ref="tree=MeSH" title="MedGen record for Torsion dystonia">Torsion dystonia</a></span><ul><li><span class="TLline"><a href="/medgen/98279" ref="tree=MeSH" title="MedGen record for Acquired idiopathic torsion dystonia">Acquired idiopathic torsion dystonia</a></span></li><li><span class="TLline"><a href="/medgen/95980" ref="tree=MeSH" title="MedGen record for Familial idiopathic torsion dystonia">Familial idiopathic torsion dystonia</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/21219" ref="tree=MeSH" title="MedGen record for Tourette syndrome">Tourette syndrome</a></span></li><li><span class="TLline"><a href="/medgen/22518" ref="tree=MeSH" title="MedGen record for Tuberous sclerosis syndrome">Tuberous sclerosis syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/325000" ref="tree=MeSH" title="MedGen record for Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis">Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis</a></span></li><li><span class="TLline"><a href="/medgen/344288" ref="tree=MeSH" title="MedGen record for Tuberous sclerosis 1">Tuberous sclerosis 1</a></span></li><li><span class="TLline"><a href="/medgen/348170" ref="tree=MeSH" title="MedGen record for Tuberous sclerosis 2">Tuberous sclerosis 2</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/155923" ref="tree=MeSH" title="MedGen record for Unverricht-Lundborg syndrome">Unverricht-Lundborg syndrome</a></span></li><li><span class="TLline"><a href="/medgen/42426" ref="tree=MeSH" title="MedGen record for Wilson disease">Wilson disease</a></span></li><li><span class="TLline"><a href="/medgen/211749" ref="tree=MeSH" title="MedGen record for X-linked intellectual disability">X-linked intellectual disability</a></span><ul><li><span class="TLline"><a href="/medgen/408200" ref="tree=MeSH" title="MedGen record for Classical Lissencephalies and Subcortical Band Heterotopias">Classical Lissencephalies and Subcortical Band Heterotopias</a></span></li><li><span class="TLline"><a href="/medgen/75556" ref="tree=MeSH" title="MedGen record for Coffin-Lowry syndrome">Coffin-Lowry syndrome</a></span></li><li><span class="TLline"><a href="/medgen/209235" ref="tree=MeSH" title="MedGen record for Danon disease">Danon disease</a></span></li><li><span class="TLline"><a href="/medgen/8912" ref="tree=MeSH" title="MedGen record for Fragile X syndrome">Fragile X syndrome</a></span></li><li><span class="TLline"><a href="/medgen/9721" ref="tree=MeSH" title="MedGen record for Lesch-Nyhan syndrome">Lesch-Nyhan syndrome</a></span></li><li><span class="TLline"><a href="/medgen/44030" ref="tree=MeSH" title="MedGen record for Menkes kinky-hair syndrome">Menkes kinky-hair syndrome</a></span></li><li><span class="TLline"><a href="/medgen/7734" ref="tree=MeSH" title="MedGen record for Mucopolysaccharidosis, MPS-II">Mucopolysaccharidosis, MPS-II</a></span></li><li><span class="TLline"><a href="/medgen/19610" ref="tree=MeSH" title="MedGen record for Pyruvate dehydrogenase complex deficiency">Pyruvate dehydrogenase complex deficiency</a></span></li><li><span class="TLline"><a href="/medgen/48441" ref="tree=MeSH" title="MedGen record for Rett syndrome">Rett syndrome</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/38785" ref="tree=MeSH" title="MedGen record for Motor neuron disease">Motor neuron disease</a></span><ul><li><span class="TLline"><a href="/medgen/274" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis">Amyotrophic lateral sclerosis</a></span><ul><li><span class="TLline"><a href="/medgen/462753" ref="tree=MeSH" title="MedGen record for Amyotrophic Lateral Sclerosis 14, With or Without Frontotemporal Dementia">Amyotrophic Lateral Sclerosis 14, With or Without Frontotemporal Dementia</a></span></li><li><span class="TLline"><a href="/medgen/400169" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 1">Amyotrophic lateral sclerosis type 1</a></span></li><li><span class="TLline"><a href="/medgen/339829" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 3">Amyotrophic lateral sclerosis type 3</a></span></li><li><span class="TLline"><a href="/medgen/355983" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 4">Amyotrophic lateral sclerosis type 4</a></span></li><li><span class="TLline"><a href="/medgen/419901" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 6">Amyotrophic lateral sclerosis type 6</a></span></li><li><span class="TLline"><a href="/medgen/334136" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 7">Amyotrophic lateral sclerosis type 7</a></span></li><li><span class="TLline"><a href="/medgen/325237" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 8">Amyotrophic lateral sclerosis type 8</a></span></li><li><span class="TLline"><a href="/medgen/395629" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 9">Amyotrophic lateral sclerosis type 9</a></span></li><li><span class="TLline"><a href="/medgen/383137" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 10">Amyotrophic lateral sclerosis type 10</a></span></li><li><span class="TLline"><a href="/medgen/393399" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 11">Amyotrophic lateral sclerosis type 11</a></span></li><li><span class="TLline"><a href="/medgen/813851" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 21">Amyotrophic lateral sclerosis type 21</a></span></li><li><span class="TLline"><a href="/medgen/1645924" ref="tree=MeSH" title="MedGen record for Amyotrophic lateral sclerosis type 23">Amyotrophic lateral sclerosis type 23</a></span></li><li><span class="TLline"><a href="/medgen/923704" ref="tree=MeSH" title="MedGen record for Juvenile amyotrophic lateral sclerosis">Juvenile amyotrophic lateral sclerosis</a></span></li><li><span class="TLline"><a href="/medgen/214634" ref="tree=MeSH" title="MedGen record for Progressive muscular atrophy">Progressive muscular atrophy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/57591" ref="tree=MeSH" title="MedGen record for Primary lateral sclerosis">Primary lateral sclerosis</a></span></li><li><span class="TLline"><a href="/medgen/18290" ref="tree=MeSH" title="MedGen record for Progressive bulbar palsy">Progressive bulbar palsy</a></span><ul><li><span class="TLline"><a href="/medgen/163239" ref="tree=MeSH" title="MedGen record for Brown-Vialetto-van Laere syndrome 1">Brown-Vialetto-van Laere syndrome 1</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/906831" ref="tree=MeSH" title="MedGen record for Progressive spinal muscular atrophy">Progressive spinal muscular atrophy</a></span></li><li><span class="TLline"><a href="/medgen/7755" ref="tree=MeSH" title="MedGen record for Spinal muscular atrophy">Spinal muscular atrophy</a></span><ul><li><span class="TLline"><a href="/medgen/870465" ref="tree=MeSH" title="MedGen record for Acute infantile spinal muscular atrophy">Acute infantile spinal muscular atrophy</a></span></li><li><span class="TLline"><a href="/medgen/101816" ref="tree=MeSH" title="MedGen record for Kugelberg-Welander disease">Kugelberg-Welander disease</a></span></li><li><span class="TLline"><a href="/medgen/21913" ref="tree=MeSH" title="MedGen record for Proximal Hereditary Motor Neuropathy Type I">Proximal Hereditary Motor Neuropathy Type I</a></span></li><li><span class="TLline"><a href="/medgen/870510" ref="tree=MeSH" title="MedGen record for Proximal spinal muscular atrophy">Proximal spinal muscular atrophy</a></span></li><li><span class="TLline"><a href="/medgen/355801" ref="tree=MeSH" title="MedGen record for Spinal muscular atrophy, segmental">Spinal muscular atrophy, segmental</a></span></li><li><span class="TLline"><a href="/medgen/95975" ref="tree=MeSH" title="MedGen record for Spinal muscular atrophy, type II">Spinal muscular atrophy, type II</a></span></li><li><span class="TLline"><a href="/medgen/325364" ref="tree=MeSH" title="MedGen record for Spinal muscular atrophy, type IV">Spinal muscular atrophy, type IV</a></span></li><li><span class="TLline"><a href="/medgen/1845578" ref="tree=MeSH" title="MedGen record for Werdnig-Hoffmann disease">Werdnig-Hoffmann disease</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/155656" ref="tree=MeSH" title="MedGen record for Paraneoplastic neurologic syndrome">Paraneoplastic neurologic syndrome</a></span><ul><li><span class="TLline"><a href="/medgen/458943" ref="tree=MeSH" title="MedGen record for Anti-NMDA receptor encephalitis">Anti-NMDA receptor encephalitis</a></span></li><li><span class="TLline"><a href="/medgen/729915" ref="tree=MeSH" title="MedGen record for Cancer-associated retinopathy">Cancer-associated retinopathy</a></span></li><li><span class="TLline"><a href="/medgen/6005" ref="tree=MeSH" title="MedGen record for Eaton-Lambert syndrome">Eaton-Lambert syndrome</a></span></li><li><span class="TLline"><a href="/medgen/137895" ref="tree=MeSH" title="MedGen record for Limbic encephalitis">Limbic encephalitis</a></span></li><li><span class="TLline"><a href="/medgen/7764" ref="tree=MeSH" title="MedGen record for Myasthenia gravis">Myasthenia gravis</a></span><ul><li><span class="TLline"><a href="/medgen/1843050" ref="tree=MeSH" title="MedGen record for Adult-onset myasthenia gravis">Adult-onset myasthenia gravis</a></span></li><li><span class="TLline"><a href="/medgen/1842990" ref="tree=MeSH" title="MedGen record for Juvenile myasthenia gravis">Juvenile myasthenia gravis</a></span></li><li><span class="TLline"><a href="/medgen/102360" ref="tree=MeSH" title="MedGen record for Neonatal myasthenia gravis">Neonatal myasthenia gravis</a></span></li><li><span class="TLline"><a href="/medgen/96918" ref="tree=MeSH" title="MedGen record for Transient neonatal myasthenia gravis">Transient neonatal myasthenia gravis</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/97955" ref="tree=MeSH" title="MedGen record for Opsoclonus-myoclonus syndrome">Opsoclonus-myoclonus syndrome</a></span></li><li><span class="TLline"><a href="/medgen/98273" ref="tree=MeSH" title="MedGen record for Paraneoplastic cerebellar degeneration">Paraneoplastic cerebellar degeneration</a></span></li><li><span class="TLline"><a href="/medgen/1842767" ref="tree=MeSH" title="MedGen record for Paraneoplastic isolated brainstem encephalitis">Paraneoplastic isolated brainstem encephalitis</a></span></li><li><span class="TLline"><a href="/medgen/124380" ref="tree=MeSH" title="MedGen record for Paraneoplastic polyneuropathy">Paraneoplastic polyneuropathy</a></span><ul><li><span class="TLline"><a href="/medgen/233843" ref="tree=MeSH" title="MedGen record for Paraneoplastic Subacute Sensory Neuronopathy">Paraneoplastic Subacute Sensory Neuronopathy</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/1842406" ref="tree=MeSH" title="MedGen record for Paraneoplastic sensory ganglionopathy">Paraneoplastic sensory ganglionopathy</a></span></li><li><span class="TLline"><a href="/medgen/6488" ref="tree=MeSH" title="MedGen record for Transverse myelitis">Transverse myelitis</a></span><ul><li><span class="TLline"><a href="/medgen/45063" ref="tree=MeSH" title="MedGen record for Neuromyelitis optica">Neuromyelitis optica</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/36363" ref="tree=MeSH" title="MedGen record for Post poliomyelitis syndrome">Post poliomyelitis syndrome</a></span></li><li><span class="TLline"><a href="/medgen/56445" ref="tree=MeSH" title="MedGen record for Prion disease">Prion disease</a></span><ul><li><span class="TLline"><a href="/medgen/38817" ref="tree=MeSH" title="MedGen record for Bovine Spongiform Encephalopathy">Bovine Spongiform Encephalopathy</a></span></li><li><span class="TLline"><a href="/medgen/7179" ref="tree=MeSH" title="MedGen record for Creutzfeldt-Jakob disease">Creutzfeldt-Jakob disease</a></span><ul><li><span class="TLline"><a href="/medgen/1826177" ref="tree=MeSH" title="MedGen record for Acquired Creutzfeldt-Jakob disease">Acquired Creutzfeldt-Jakob disease</a></span></li><li><span class="TLline"><a href="/medgen/155837" ref="tree=MeSH" title="MedGen record for Inherited Creutzfeldt-Jakob disease">Inherited Creutzfeldt-Jakob disease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/104768" ref="tree=MeSH" title="MedGen record for Fatal familial insomnia">Fatal familial insomnia</a></span></li><li><span class="TLline"><a href="/medgen/9653" ref="tree=MeSH" title="MedGen record for Kuru">Kuru</a></span></li><li><span class="TLline"><a href="/medgen/19903" ref="tree=MeSH" title="MedGen record for Scrapie">Scrapie</a></span></li><li><span class="TLline"><a href="/medgen/138163" ref="tree=MeSH" title="MedGen record for Variant Creutzfeldt-Jakob disease">Variant Creutzfeldt-Jakob disease</a></span></li><li><span class="TLline"><a href="/medgen/211688" ref="tree=MeSH" title="MedGen record for Wasting Disease, Chronic">Wasting Disease, Chronic</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/113144" ref="tree=MeSH" title="MedGen record for Subacute combined degeneration of spinal cord">Subacute combined degeneration of spinal cord</a></span></li><li><span class="TLline"><a href="/medgen/1682194" ref="tree=MeSH" title="MedGen record for Synucleinopathy">Synucleinopathy</a></span><ul><li><span class="TLline"><a href="/medgen/199874" ref="tree=MeSH" title="MedGen record for Lewy body dementia">Lewy body dementia</a></span></li><li><span class="TLline"><a href="/medgen/98276" ref="tree=MeSH" title="MedGen record for Multiple system atrophy">Multiple system atrophy</a></span><ul><li><span class="TLline"><a href="/medgen/1843304" ref="tree=MeSH" title="MedGen record for Multiple system atrophy, cerebellar type">Multiple system atrophy, cerebellar type</a></span></li><li><span class="TLline"><a href="/medgen/1842393" ref="tree=MeSH" title="MedGen record for Multiple system atrophy, parkinsonian type">Multiple system atrophy, parkinsonian type</a></span></li><li><span class="TLline"><a href="/medgen/20740" ref="tree=MeSH" title="MedGen record for Shy Drager Syndrome">Shy Drager Syndrome</a></span></li><li><span class="TLline"><a href="/medgen/124366" ref="tree=MeSH" title="MedGen record for Striatonigral degeneration">Striatonigral degeneration</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/10590" ref="tree=MeSH" title="MedGen record for Parkinson disease">Parkinson disease</a></span><ul><li><span class="TLline"><a href="/medgen/357008" ref="tree=MeSH" title="MedGen record for Autosomal dominant Parkinson disease 1">Autosomal dominant Parkinson disease 1</a></span></li><li><span class="TLline"><a href="/medgen/381361" ref="tree=MeSH" title="MedGen record for Autosomal dominant Parkinson disease 4">Autosomal dominant Parkinson disease 4</a></span></li><li><span class="TLline"><a href="/medgen/339628" ref="tree=MeSH" title="MedGen record for Autosomal dominant Parkinson disease 8">Autosomal dominant Parkinson disease 8</a></span></li><li><span class="TLline"><a href="/medgen/342982" ref="tree=MeSH" title="MedGen record for Autosomal recessive early-onset Parkinson disease 6">Autosomal recessive early-onset Parkinson disease 6</a></span></li><li><span class="TLline"><a href="/medgen/344049" ref="tree=MeSH" title="MedGen record for Autosomal recessive early-onset Parkinson disease 7">Autosomal recessive early-onset Parkinson disease 7</a></span></li><li><span class="TLline"><a href="/medgen/401500" ref="tree=MeSH" title="MedGen record for Autosomal recessive juvenile Parkinson disease 2">Autosomal recessive juvenile Parkinson disease 2</a></span></li><li><span class="TLline"><a href="/medgen/414488" ref="tree=MeSH" title="MedGen record for Autosomal recessive Parkinson disease 14">Autosomal recessive Parkinson disease 14</a></span></li><li><span class="TLline"><a href="/medgen/66768" ref="tree=MeSH" title="MedGen record for Juvenile paralysis agitans of Hunt">Juvenile paralysis agitans of Hunt</a></span></li><li><span class="TLline"><a href="/medgen/338281" ref="tree=MeSH" title="MedGen record for Kufor-Rakeb syndrome">Kufor-Rakeb syndrome</a></span></li><li><span class="TLline"><a href="/medgen/409973" ref="tree=MeSH" title="MedGen record for Parkinson disease 6">Parkinson disease 6</a></span></li><li><span class="TLline"><a href="/medgen/339741" ref="tree=MeSH" title="MedGen record for Parkinson disease 10">Parkinson disease 10</a></span></li><li><span class="TLline"><a href="/medgen/896658" ref="tree=MeSH" title="MedGen record for Parkinson disease 11, autosomal dominant, susceptibility to">Parkinson disease 11, autosomal dominant, susceptibility to</a></span></li><li><span class="TLline"><a href="/medgen/337173" ref="tree=MeSH" title="MedGen record for Parkinson disease 12">Parkinson disease 12</a></span></li><li><span class="TLline"><a href="/medgen/343992" ref="tree=MeSH" title="MedGen record for Parkinson disease 13, autosomal dominant, susceptibility to">Parkinson disease 13, autosomal dominant, susceptibility to</a></span></li><li><span class="TLline"><a href="/medgen/442620" ref="tree=MeSH" title="MedGen record for Parkinson disease 16">Parkinson disease 16</a></span></li><li><span class="TLline"><a href="/medgen/481763" ref="tree=MeSH" title="MedGen record for Parkinson disease 17">Parkinson disease 17</a></span></li><li><span class="TLline"><a href="/medgen/355499" ref="tree=MeSH" title="MedGen record for Parkinson disease 3, autosomal dominant">Parkinson disease 3, autosomal dominant</a></span></li><li><span class="TLline"><a href="/medgen/462249" ref="tree=MeSH" title="MedGen record for Parkinson disease 5, autosomal dominant, susceptibility to">Parkinson disease 5, autosomal dominant, susceptibility to</a></span></li><li><span class="TLline"><a href="/medgen/463618" ref="tree=MeSH" title="MedGen record for Parkinson disease, late-onset">Parkinson disease, late-onset</a></span></li><li><span class="TLline"><a href="/medgen/333199" ref="tree=MeSH" title="MedGen record for Parkinson disease, mitochondrial">Parkinson disease, mitochondrial</a></span></li><li><span class="TLline"><a href="/medgen/337969" ref="tree=MeSH" title="MedGen record for Parkinsonian-pyramidal syndrome">Parkinsonian-pyramidal syndrome</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/181880" ref="tree=MeSH" title="MedGen record for Tauopathy">Tauopathy</a></span><ul><li><span class="TLline"><a href="/medgen/1853" ref="tree=MeSH" title="MedGen record for Alzheimer disease">Alzheimer disease</a></span><ul><li><span class="TLline"><a href="/medgen/400197" ref="tree=MeSH" title="MedGen record for Alzheimer disease 2">Alzheimer disease 2</a></span></li><li><span class="TLline"><a href="/medgen/334304" ref="tree=MeSH" title="MedGen record for Alzheimer disease 3">Alzheimer disease 3</a></span></li><li><span class="TLline"><a href="/medgen/376072" ref="tree=MeSH" title="MedGen record for Alzheimer disease 4">Alzheimer disease 4</a></span></li><li><span class="TLline"><a href="/medgen/381362" ref="tree=MeSH" title="MedGen record for Alzheimer disease 6">Alzheimer disease 6</a></span></li><li><span class="TLline"><a href="/medgen/342907" ref="tree=MeSH" title="MedGen record for Alzheimer disease 7">Alzheimer disease 7</a></span></li><li><span class="TLline"><a href="/medgen/375956" ref="tree=MeSH" title="MedGen record for Alzheimer disease 8">Alzheimer disease 8</a></span></li><li><span class="TLline"><a href="/medgen/924255" ref="tree=MeSH" title="MedGen record for Alzheimer disease 9">Alzheimer disease 9</a></span></li><li><span class="TLline"><a href="/medgen/351228" ref="tree=MeSH" title="MedGen record for Alzheimer disease 10">Alzheimer disease 10</a></span></li><li><span class="TLline"><a href="/medgen/377886" ref="tree=MeSH" title="MedGen record for Alzheimer disease 11">Alzheimer disease 11</a></span></li><li><span class="TLline"><a href="/medgen/410013" ref="tree=MeSH" title="MedGen record for Alzheimer disease 12">Alzheimer disease 12</a></span></li><li><span class="TLline"><a href="/medgen/370835" ref="tree=MeSH" title="MedGen record for Alzheimer disease 13">Alzheimer disease 13</a></span></li><li><span class="TLline"><a href="/medgen/369666" ref="tree=MeSH" title="MedGen record for Alzheimer disease 14">Alzheimer disease 14</a></span></li><li><span class="TLline"><a href="/medgen/394384" ref="tree=MeSH" title="MedGen record for Alzheimer disease 16">Alzheimer disease 16</a></span></li><li><span class="TLline"><a href="/medgen/767366" ref="tree=MeSH" title="MedGen record for Alzheimer disease 17">Alzheimer disease 17</a></span></li><li><span class="TLline"><a href="/medgen/346983" ref="tree=MeSH" title="MedGen record for Alzheimer disease without neurofibrillary tangles">Alzheimer disease without neurofibrillary tangles</a></span></li><li><span class="TLline"><a href="/medgen/448010" ref="tree=MeSH" title="MedGen record for Early-onset autosomal dominant Alzheimer disease">Early-onset autosomal dominant Alzheimer disease</a></span></li></ul></li><li><span class="TLline"><a href="/medgen/95979" ref="tree=MeSH" title="MedGen record for Corticobasal degeneration disorder">Corticobasal degeneration disorder</a></span></li><li><span class="TLline"><a href="/medgen/403960" ref="tree=MeSH" title="MedGen record for Diffuse Neurofibrillary Tangles with Calcification">Diffuse Neurofibrillary Tangles with Calcification</a></span></li><li><span class="TLline"><a href="/medgen/21026" ref="tree=MeSH" title="MedGen record for Progressive supranuclear palsy">Progressive supranuclear palsy</a></span><ul><li><span class="TLline"><a href="/medgen/1779597" ref="tree=MeSH" title="MedGen record for Atypical progressive supranuclear palsy syndrome">Atypical progressive supranuclear palsy syndrome</a></span></li><li><span class="TLline"><a href="/medgen/1640811" ref="tree=MeSH" title="MedGen record for Supranuclear palsy, progressive, 1">Supranuclear palsy, progressive, 1</a></span></li><li><span class="TLline"><a href="/medgen/324446" ref="tree=MeSH" title="MedGen record for Supranuclear palsy, progressive, 2">Supranuclear palsy, progressive, 2</a></span></li><li><span class="TLline"><a href="/medgen/370922" ref="tree=MeSH" title="MedGen record for Supranuclear palsy, progressive, 3">Supranuclear palsy, progressive, 3</a></span></li></ul></li></ul></li><li><span class="TLline"><a href="/medgen/439336" ref="tree=MeSH" title="MedGen record for TDP-43 proteinopathy">TDP-43 proteinopathy</a></span><ul><li><span class="TLline"><a href="/medgen/148228" ref="tree=MeSH" title="MedGen record for Degenerations, Frontotemporal Lobar">Degenerations, Frontotemporal Lobar</a></span><ul><li><span class="TLline"><a href="/medgen/83266" ref="tree=MeSH" title="MedGen record for Frontotemporal dementia">Frontotemporal dementia</a></span></li><li><span class="TLline"><a href="/medgen/148373" ref="tree=MeSH" title="MedGen record for Primary progressive non fluent aphasia">Primary progressive non fluent aphasia</a></span></li></ul></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_105">
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<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>
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<div class="nl"><a target="_blank" href="/pubmed/34963139">Physical Therapist Management of Parkinson Disease: A Clinical Practice Guideline From the American Physical Therapy Association.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Osborne JA,
|
||
Botkin R,
|
||
Colon-Semenza C,
|
||
DeAngelis TR,
|
||
Gallardo OG,
|
||
Kosakowski H,
|
||
Martello J,
|
||
Pradhan S,
|
||
Rafferty M,
|
||
Readinger JL,
|
||
Whitt AL,
|
||
Ellis TD</span><br />
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||
<span class="medgenPMjournal">Phys Ther</span>
|
||
2022 Apr 1;102(4)
|
||
doi: 10.1093/ptj/pzab302.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34963139" target="_blank">34963139</a><a href="/pmc/articles/PMC9046970" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/34399110">Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Northrup H,
|
||
Aronow ME,
|
||
Bebin EM,
|
||
Bissler J,
|
||
Darling TN,
|
||
de Vries PJ,
|
||
Frost MD,
|
||
Fuchs Z,
|
||
Gosnell ES,
|
||
Gupta N,
|
||
Jansen AC,
|
||
Jóźwiak S,
|
||
Kingswood JC,
|
||
Knilans TK,
|
||
McCormack FX,
|
||
Pounders A,
|
||
Roberds SL,
|
||
Rodriguez-Buritica DF,
|
||
Roth J,
|
||
Sampson JR,
|
||
Sparagana S,
|
||
Thiele EA,
|
||
Weiner HL,
|
||
Wheless JW,
|
||
Towbin AJ,
|
||
Krueger DA;
|
||
International Tuberous Sclerosis Complex Consensus Group</span><br />
|
||
<span class="medgenPMjournal">Pediatr Neurol</span>
|
||
2021 Oct;123:50-66.
|
||
Epub 2021 Jul 24
|
||
doi: 10.1016/j.pediatrneurol.2021.07.011.
|
||
<span class="bold">PMID: </span><a href="/pubmed/34399110" target="_blank">34399110</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/26474316">MDS clinical diagnostic criteria for Parkinson's disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Postuma RB,
|
||
Berg D,
|
||
Stern M,
|
||
Poewe W,
|
||
Olanow CW,
|
||
Oertel W,
|
||
Obeso J,
|
||
Marek K,
|
||
Litvan I,
|
||
Lang AE,
|
||
Halliday G,
|
||
Goetz CG,
|
||
Gasser T,
|
||
Dubois B,
|
||
Chan P,
|
||
Bloem BR,
|
||
Adler CH,
|
||
Deuschl G</span><br />
|
||
<span class="medgenPMjournal">Mov Disord</span>
|
||
2015 Oct;30(12):1591-601.
|
||
doi: 10.1002/mds.26424.
|
||
<span class="bold">PMID: </span><a href="/pubmed/26474316" target="_blank">26474316</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(degenerative%20disease%20of%20nervous%20system%2C%20unspecified)%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 (15577)</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/36361643">Neurodegenerative Diseases: From Molecular Basis to Therapy.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Agnello L,
|
||
Ciaccio M</span><br />
|
||
<span class="medgenPMjournal">Int J Mol Sci</span>
|
||
2022 Oct 25;23(21)
|
||
doi: 10.3390/ijms232112854.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36361643" target="_blank">36361643</a><a href="/pmc/articles/PMC9654859" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/33302541">Comprehensive Review on Alzheimer's Disease: Causes and Treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Breijyeh Z,
|
||
Karaman R</span><br />
|
||
<span class="medgenPMjournal">Molecules</span>
|
||
2020 Dec 8;25(24)
|
||
doi: 10.3390/molecules25245789.
|
||
<span class="bold">PMID: </span><a href="/pubmed/33302541" target="_blank">33302541</a><a href="/pmc/articles/PMC7764106" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/31501588">Ageing as a risk factor for neurodegenerative disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Hou Y,
|
||
Dan X,
|
||
Babbar M,
|
||
Wei Y,
|
||
Hasselbalch SG,
|
||
Croteau DL,
|
||
Bohr VA</span><br />
|
||
<span class="medgenPMjournal">Nat Rev Neurol</span>
|
||
2019 Oct;15(10):565-581.
|
||
Epub 2019 Sep 9
|
||
doi: 10.1038/s41582-019-0244-7.
|
||
<span class="bold">PMID: </span><a href="/pubmed/31501588" target="_blank">31501588</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/30261683">Ageing, Cellular Senescence and Neurodegenerative Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Kritsilis M,
|
||
V Rizou S,
|
||
Koutsoudaki PN,
|
||
Evangelou K,
|
||
Gorgoulis VG,
|
||
Papadopoulos D</span><br />
|
||
<span class="medgenPMjournal">Int J Mol Sci</span>
|
||
2018 Sep 27;19(10)
|
||
doi: 10.3390/ijms19102937.
|
||
<span class="bold">PMID: </span><a href="/pubmed/30261683" target="_blank">30261683</a><a href="/pmc/articles/PMC6213570" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/17051205">Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Lin MT,
|
||
Beal MF</span><br />
|
||
<span class="medgenPMjournal">Nature</span>
|
||
2006 Oct 19;443(7113):787-95.
|
||
doi: 10.1038/nature05292.
|
||
<span class="bold">PMID: </span><a href="/pubmed/17051205" target="_blank">17051205</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Degenerative%20Disease%20of%20Nervous%20System%2C%20Unspecified%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 (110117)</a></div><h3 class="subhead">Diagnosis</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/37269450">An Update on Apraxia of Speech.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Utianski RL,
|
||
Josephs KA</span><br />
|
||
<span class="medgenPMjournal">Curr Neurol Neurosci Rep</span>
|
||
2023 Jul;23(7):353-359.
|
||
Epub 2023 Jun 3
|
||
doi: 10.1007/s11910-023-01275-1.
|
||
<span class="bold">PMID: </span><a href="/pubmed/37269450" target="_blank">37269450</a><a href="/pmc/articles/PMC10629164" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/35596580">Epilepsy in neurodegenerative diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Neri S,
|
||
Mastroianni G,
|
||
Gardella E,
|
||
Aguglia U,
|
||
Rubboli G</span><br />
|
||
<span class="medgenPMjournal">Epileptic Disord</span>
|
||
2022 Apr 1;24(2):249-273.
|
||
doi: 10.1684/epd.2021.1406.
|
||
<span class="bold">PMID: </span><a href="/pubmed/35596580" target="_blank">35596580</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29904888">Olfactory Dysfunction in Neurodegenerative Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Marin C,
|
||
Vilas D,
|
||
Langdon C,
|
||
Alobid I,
|
||
López-Chacón M,
|
||
Haehner A,
|
||
Hummel T,
|
||
Mullol J</span><br />
|
||
<span class="medgenPMjournal">Curr Allergy Asthma Rep</span>
|
||
2018 Jun 15;18(8):42.
|
||
doi: 10.1007/s11882-018-0796-4.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29904888" target="_blank">29904888</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28716886">Clinical Neurology and Epidemiology of the Major Neurodegenerative Diseases.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Erkkinen MG,
|
||
Kim MO,
|
||
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<div class="nl"><a target="_blank" href="/pubmed/30760888">Tryptophan metabolism as a common therapeutic target in cancer, neurodegeneration and beyond.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/28552366">Amyotrophic lateral sclerosis.</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Degenerative%20Disease%20of%20Nervous%20System%2C%20Unspecified%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 (52089)</a></div><h3 class="subhead">Clinical prediction guides</h3>
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<div class="nl"><a target="_blank" href="/pubmed/28062563">Pathology of Neurodegenerative Diseases.</a></div>
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Degenerative%20Disease%20of%20Nervous%20System%2C%20Unspecified%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 (90408)</a></div></div>
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|
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<div class="portlet mgSection" id="ID_104">
|
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<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>
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<div class="portlet_content ln">
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<div class="nl"><a target="_blank" href="/pubmed/35445419">The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Wenning GK,
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Stankovic I,
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Vignatelli L,
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Fanciulli A,
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Calandra-Buonaura G,
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Seppi K,
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Palma JA,
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Meissner WG,
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Krismer F,
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Berg D,
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Cortelli P,
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Freeman R,
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Halliday G,
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Höglinger G,
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Lang A,
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Ling H,
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Litvan I,
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Low P,
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Miki Y,
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Panicker J,
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Pellecchia MT,
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Quinn N,
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Sakakibara R,
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Stamelou M,
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Tolosa E,
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Tsuji S,
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Warner T,
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Epub 2022 Apr 21
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<span class="bold">PMID: </span><a href="/pubmed/35445419" target="_blank">35445419</a><a href="/pmc/articles/PMC9321158" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34456336">The Amyloid-β Pathway in Alzheimer's Disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Hampel H,
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Hardy J,
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Blennow K,
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Chen C,
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Perry G,
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Kim SH,
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Villemagne VL,
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Aisen P,
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Vendruscolo M,
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Iwatsubo T,
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Masters CL,
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Cho M,
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Lannfelt L,
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Cummings JL,
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Vergallo A</span><br />
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<span class="medgenPMjournal">Mol Psychiatry</span>
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2021 Oct;26(10):5481-5503.
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Epub 2021 Aug 30
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<div class="nl"><a target="_blank" href="/pubmed/33372386">Quality of life in Parkinson's disease: A systematic review and meta-analysis of comparative studies.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Zhao N,
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Yang Y,
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Zhang L,
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Zhang Q,
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Balbuena L,
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Ungvari GS,
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Zang YF,
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Xiang YT</span><br />
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<span class="medgenPMjournal">CNS Neurosci Ther</span>
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2021 Mar;27(3):270-279.
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Epub 2020 Dec 28
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<span class="bold">PMID: </span><a href="/pubmed/33372386" target="_blank">33372386</a><a href="/pmc/articles/PMC7871788" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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|
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<div class="nl"><a target="_blank" href="/pubmed/31684843">Effect of nutrition on neurodegenerative diseases. A systematic review.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Bianchi VE,
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Herrera PF,
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Laura R</span><br />
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2021 Oct;24(10):810-834.
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Epub 2019 Nov 4
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<span class="bold">PMID: </span><a href="/pubmed/31684843" target="_blank">31684843</a></div>
|
||
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||
<div class="nl"><a target="_blank" href="/pubmed/31209456">The Mediterranean, Dietary Approaches to Stop Hypertension (DASH), and Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Diets Are Associated with Less Cognitive Decline and a Lower Risk of Alzheimer's Disease-A Review.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">van den Brink AC,
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Brouwer-Brolsma EM,
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Berendsen AAM,
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van de Rest O</span><br />
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<span class="bold">PMID: </span><a href="/pubmed/31209456" target="_blank">31209456</a><a href="/pmc/articles/PMC6855954" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22Degenerative%20Disease%20of%20Nervous%20System%2C%20Unspecified%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 (4680)</a></div></div>
|
||
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|
||
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