Cervical spondylotic myelopathy and Kennedy syndrome mimicking amyotrophic lateral sclerosis [3]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 71, Issue 3, 2001, Pages 414-

  Fischer, D ^a   Wullner U ^a   Klockgether, T ^a   Schroder R ^a   Wilhelm, K ^a  

^a UNIVERSITY OF BONN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; CASE REPORT; CERVICAL SPONDYLOSIS; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; ELECTROMYOGRAPHY; GENETIC ANALYSIS; HUMAN; KENNEDY DISEASE; LETTER; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SPINAL CORD DISEASE; TENDON REFLEX; CERVICAL SPINE; DIAGNOSTIC ERROR; GENETICS; MIDDLE AGED; MUSCLE DISEASE; MUTATION; SPINAL MUSCULAR ATROPHY; SPONDYLOSIS;

AMYOTROPHIC LATERAL SCLEROSIS; CERVICAL VERTEBRAE; DIAGNOSIS, DIFFERENTIAL; DIAGNOSTIC ERRORS; ELECTROMYOGRAPHY; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MUSCULAR ATROPHY, SPINAL; MUSCULAR DISEASES; MUTATION; RECEPTORS, ANDROGEN; SPINAL OSTEOPHYTOSIS;

EID: 0034885164     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.71.3.414     Document Type: Letter

References (4)

1. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
2. Progressive proximal spinal and bulbar muscular atrophy of late onset: A sex-linked recessive trait
3. X-linked recessive bulbospinal neuronopathy: A clinicopathological study
4. Spinal and bulbar muscular atrophy: A trinucleotide-repeat expansion neurodegenerative disease