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

Journal of Neurology Neurosurgery and Psychiatry

Volumn 69, Issue 2, 2000, Pages 277-

  Buecking, A ^a   Pfister, R ^a  

^a Zentralklinikum Augsburg ^*  (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

ADULT; ATAXIA; CLINICAL ARTICLE; CLINICAL FEATURE; HUMAN; LETTER; MALE; NERVE POTENTIAL; NEUROPATHY; ONSET AGE; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT; X CHROMOSOME LINKAGE;

ADULT; DISEASE PROGRESSION; ELECTROMYOGRAPHY; GAIT ATAXIA; GENES, RECESSIVE; HUMANS; MALE; MIDDLE AGED; MUSCULAR ATROPHY, SPINAL; RECEPTORS, ANDROGEN; TRINUCLEOTIDE REPEAT EXPANSION; X CHROMOSOME;

EID: 0033911038     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.69.2.277     Document Type: Letter

References (5)