Sensory ataxia as the initial clinical symptom in X-linked recessive bulbospinal neuronopathy.

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Serval ID
serval:BIB_AA79580F2F21
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Production externe
Title
Sensory ataxia as the initial clinical symptom in X-linked recessive bulbospinal neuronopathy.
Journal
Journal of Neurology, Neurosurgery, and Psychiatry
Author(s)
Buecking A., Pfister R.
ISSN
0022-3050 (Print)
ISSN-L
0022-3050
Publication state
Published
Issued date
2000
Peer-reviewed
Oui
Volume
69
Number
2
Pages
277
Language
english
Notes
Publication types: Case Reports ; LetterPublication Status: ppublish
Keywords
Adult, Disease Progression, Electromyography, Gait Ataxia/etiology, Genes, Recessive, Humans, Male, Middle Aged, Muscular Atrophy, Spinal/diagnosis, Muscular Atrophy, Spinal/genetics, Receptors, Androgen/genetics, Trinucleotide Repeat Expansion/genetics, X Chromosome
Pubmed
10960290
Create date
12/07/2013 11:24
Last modification date
20/08/2019 16:14
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