Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis

Muscle and Nerve

Volumn 23, Issue 10, 2000, Pages 1472-1487

  Lewis, Richard A ^a   Sumner, Austin J ^b   Shy, Michael E ^a  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b LOUISIANA STATE UNIV MEDICAL CENTER   (United States)

Author keywords

Charcot Marie Tooth disease; Dejerine Sottas disease; Electrodiagnosis; Hereditary neuropathy with liability to pressure palsies; Inherited neuropathies; Pelizaeus Merzbacher disease

Indexed keywords

MYELIN;

DEMYELINATING NEUROPATHY; ELECTRODIAGNOSIS; ELECTROPHYSIOLOGY; GENE MUTATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; NERVE CONDUCTION; PELIZAEUS MERZBACHER DISEASE; PRIORITY JOURNAL; REVIEW;

EID: 0033809078     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-4598(200010)23:10<1472::aid-mus3>3.0.co;2-%23     Document Type: Review

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