The natural history of Charcot-Marie-Tooth type 1A in adults: A 5-year follow-up study

Brain

Volumn 132, Issue 12, 2009, Pages 3252-3262

  Verhamme, Camiel ^a   Van Schaik, Ivo N ^a   Koelman, Johannes H T M ^a   De Haan, Rob J ^a   De Visser, Marianne ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

Axonal dysfunction; Charcot Marie Tooth Disease; Charcot Marie Tooth Disease type 1A; Hereditary motor and sensory neuropathies; Hereditary motor and sensory neuropathy type Ia; Natural history; Peripheral neuropathies

Indexed keywords

ADOLESCENT; ADULT; AGED; AGING; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; ELECTROMYOGRAM; FEMALE; FOLLOW UP; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MOTOR NERVE CONDUCTION; MUSCLE ACTION POTENTIAL; MUSCLE STRENGTH; MUSCLE WEAKNESS; NERVE CONDUCTION; PHYSICAL DISABILITY; PRIORITY JOURNAL; SCORING SYSTEM;

ACTION POTENTIALS; ADOLESCENT; ADULT; AGED; AXONS; CHARCOT-MARIE-TOOTH DISEASE; COHORT STUDIES; DISABILITY EVALUATION; DISEASE PROGRESSION; ELECTRODIAGNOSIS; ELECTROMYOGRAPHY; FEMALE; FOLLOW-UP STUDIES; HUMANS; MALE; MIDDLE AGED; MUSCLE STRENGTH; MUSCLE WEAKNESS; MUSCLE, SKELETAL; NEURAL CONDUCTION; PERIPHERAL NERVES; PREDICTIVE VALUE OF TESTS; SEVERITY OF ILLNESS INDEX; TIME FACTORS; YOUNG ADULT;

EID: 71049153213     PISSN: 00068950     EISSN: 14602156     Source Type: Journal    
DOI: 10.1093/brain/awp251     Document Type: Article

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