Comparison of CMT1A and CMT2: Similarities and differences

Journal of Neurology

Volumn 253, Issue 12, 2006, Pages 1572-1580

  Bienfait, Henriette M E ^a   Verhamme, Camiel ^a   Van Schaik, Ivo N ^a,b   Koelman, Johannes H T M ^a   De Visser, Bram W Ongerboer ^a   De Haan, Rob J ^a   Baas, Frank ^a   Van Engelen, Baziel G M ^c   De Visser, Marianne ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

^b Onze Lieve Vrouwe Gasthuis ^*  (Netherlands)

^c RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Charcot Marie Tooth disease; Demyelination; Hereditary neuropathy; Nerve conduction study

Indexed keywords

ADULT; AGED; AREFLEXIA; ARTICLE; AXONAL INJURY; CHARCOT MARIE TOOTH DISEASE 1A; CHARCOT MARIE TOOTH DISEASE 2; CHILD; COMPARATIVE STUDY; DEMYELINATION; ELECTRODIAGNOSIS; ELECTROPHYSIOLOGY; FEMALE; FOOT MALFORMATION; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MAJOR CLINICAL STUDY; MALE; MEDIAN NERVE; MOLECULAR GENETICS; MOTOR NERVE CONDUCTION; MUSCLE ACTION POTENTIAL; MUSCLE WEAKNESS; PHENOTYPE; POST HOC ANALYSIS; PRIORITY JOURNAL; SENSORY NERVE CONDUCTION; SYSTEMATIC REVIEW;

ACTION POTENTIALS; ADOLESCENT; ADULT; AGE OF ONSET; AGED; CHARCOT-MARIE-TOOTH DISEASE; CHILD; FEMALE; HUMANS; MALE; MEDIAN NERVE; MIDDLE AGED; NEURAL CONDUCTION; STATISTICS, NONPARAMETRIC;

EID: 33846303532     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-006-0260-6     Document Type: Article

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