X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode.
about
The genetics of Charcot-Marie-Tooth disease: current trends and future implications for diagnosis and managementGap junctions in inherited human disorders of the central nervous system.Recurrent Episodes of Stroke-Like Symptoms in a Patient with Charcot-Marie-Tooth Neuropathy X Type 1.Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease.Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case reportThe central nervous system phenotype of X-linked Charcot-Marie-Tooth disease: a transient disorder of children and young adults.A new mutation in GJC2 associated with subclinical leukodystrophy.Episodic neurological dysfunction in hereditary peripheral neuropathyStroke and Stroke-like Episodes in Muscle Disease.Loss of Coupling Distinguishes GJB1 Mutations Associated with CNS Manifestations of CMT1X from Those Without CNS Manifestations.GJB1-associated X-linked Charcot-Marie-Tooth disease, a disorder affecting the central and peripheral nervous systems.A Review of X-linked Charcot-Marie-Tooth Disease.Cerebral Manifestations of Mitochondrial Disorders.X-linked Charcot-Marie-Tooth type 1: stroke-like presentation of a novel GJB1 mutation.CNS involvement in CMTX1 caused by a novel connexin 32 mutation: a 6-year follow-up in neuroimaging and nerve conduction.Recurrent central nervous system white matter changes in charcot-Marie-tooth type X disease.
P2860
Q26777319-16EB20EC-FC0F-40BE-B6A5-947F9157A2D9Q26823332-EF5A5451-B78F-4E3A-8600-551A5E8EAAB1Q30388874-68FFB56B-8417-4725-811E-355576E29E33Q33646656-88568327-DEDF-4093-A6D2-92859B1C480AQ34038303-3A7EE8F2-795A-48DD-8BED-95A0AE14993DQ34582703-D102C292-D87F-43EA-903A-AC63904A78D1Q34994055-6BAF0E15-24A4-4C30-9E68-DD050C7F2A15Q35149122-9A203B8E-2509-4FCD-879F-2355C52384E5Q36041117-35CA32D2-69FE-40FA-8EFE-5BE805F62663Q37576096-CA1D3CD6-1F7F-43DA-9E44-A4D8031AD60BQ38265030-53F45F64-2ED6-4B7B-B3EF-3CC735F64257Q38589445-9F5955B3-DF66-4527-AC48-C31E8646F751Q47640125-C572CEB1-DCED-4159-9C4B-9C5F7D6034D7Q48765259-FC2DAB9A-63E9-4B10-B5DE-3DFC8E0AD082Q52138934-D8A2FE7D-F76D-46E0-8D93-F26CCF4F8491Q53084843-3B94B479-5739-4824-B664-4FBD443D4E9D
P2860
X-linked hereditary motor sensory neuropathy (type 1) presenting with a stroke-like episode.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
@zh
2010年學術文章
@zh-hant
name
X-linked hereditary motor sens ...... ng with a stroke-like episode.
@en
X-linked hereditary motor sensory neuropathy
@nl
type
label
X-linked hereditary motor sens ...... ng with a stroke-like episode.
@en
X-linked hereditary motor sensory neuropathy
@nl
prefLabel
X-linked hereditary motor sens ...... ng with a stroke-like episode.
@en
X-linked hereditary motor sensory neuropathy
@nl
P2093
P2860
P1476
X-linked hereditary motor sens ...... ng with a stroke-like episode.
@en
P2093
Anuruddha Padeniya
Carl Fratter
David Roberts
Geetha Anand
Marjo van der Knaap
Michele Hamilton-Ayers
Nitin Maheshwari
Sandeep Jayawant
P2860
P304
P356
10.1111/J.1469-8749.2010.03674.X
P577
2010-05-14T00:00:00Z