Very late onset X-linked recessive bulbospinal neuronopathy: mild clinical features and a mild increase in the size of tandem CAG repeat in androgen receptor gene.

Lignende værker

• Central motor and sensory conduction in X-linked recessive bulbospinal neuronopathy.
  af: Kachi, T, et al.
  Udgivet: (1992)
• X-linked recessive bulbospinal neuronopathy: a report of ten cases.
  af: Harding, A E, et al.
  Udgivet: (1982)
• Sensory ataxia as the initial clinical symptom in X-linked recessive bulbospinal neuronopathy
  af: BUECKING, A., et al.
  Udgivet: (2000)
• Sandhoff disease mimicking adult-onset bulbospinal neuronopathy.
  af: Thomas, P K, et al.
  Udgivet: (1989)
• Tissue-Specific Somatic Mosaicism in Spinal and Bulbar Muscular Atrophy Is Dependent on CAG-Repeat Length and Androgen Receptor–Gene Expression Level
  af: Tanaka, Fumiaki, et al.
  Udgivet: (1999)