Charcot-Marie-Tooth disease – muscle biopsy findings in relation to neurophysiology

This publication has 16 references indexed in Scilit:

• Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
  Human Molecular Genetics, 1993
• Localization of a Gene (CMT2A) for Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 to Chromosome 1p and Evidence of Genetic Heterogeneity
  Genomics, 1993
• Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region
  Human Genetics, 1991
• Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
  Neuromuscular Disorders, 1991
• Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17
  Experimental Neurology, 1989
• PERONEAL MUSCULAR ATROPHY (PMA) AND RELATED DISORDERS
  Brain, 1977
• LONGITUDINAL FIBRE SPLITTING IN NEUROGENIC MUSCULAR DISORDERS—ITS RELATION TO THE PATHOGENESIS OF ‘MYOPATHIC’ CHANGE
  Brain, 1976
• "Myopathic" Changes in Chronically Denervated Muscle
  Archives of Neurology, 1967
• Rapid examination of muscle tissue
  Neurology, 1963
• PATHOLOGICAL CHANGES IN MUSCLE BIOPSIES FROM PATIENTS WITH PERONEAL MUSCULAR ATROPHY
  Brain, 1960