Clinico-electrophysiological correlation of extensor digitorum brevis muscle atrophy in children with Charcot-Marie-Tooth disease 1A duplication

Neuromuscular Disorders

Volumn 10, Issue 6, 2000, Pages 419-424

  Berciano, José ^a   García, Antonio ^a   Calleja, Jesús ^a   Combarros, Onofre ^a  

^a HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

Author keywords

Axonal degeneration; Charcot Marie Tooth disease; Chromosome 17 duplication; Muscular atrophy; Nerve conduction velocity

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHROMOSOME 17; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; ELECTROPHYSIOLOGY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; INFANT; MUSCLE ACTION POTENTIAL; MUSCLE ATROPHY; NERVE CONDUCTION; NERVE FIBER DEGENERATION; PERONEUS NERVE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

ACTION POTENTIALS; ADOLESCENT; ADULT; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHILD, PRESCHOOL; DISEASE PROGRESSION; ELECTROPHYSIOLOGY; FEMALE; GENE DUPLICATION; HUMANS; INFANT; LONGITUDINAL STUDIES; MALE; MUSCLE, SKELETAL; MUSCULAR ATROPHY; NEURAL CONDUCTION; PERONEAL NERVE; PROSPECTIVE STUDIES;

EID: 0034255676     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(99)00114-5     Document Type: Article

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