Correlation between weakness and axonal loss in patients with CMT1A

Annals of the New York Academy of Sciences

Volumn 883, Issue , 1999, Pages 490-492

  Krajewski, Karen ^a   Turansky, Cheryl ^a   Lewis, Richard ^a   Garbern, James ^a   Hinderer, Steven ^a   Kamholz, John ^a   Shy, Michael E ^a  

^a HENRY FORD HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; DISEASE COURSE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MIDDLE AGED; NERVE CONDUCTION; NERVE FIBER; PATHOLOGY; PATHOPHYSIOLOGY; PRESCHOOL CHILD;

ADOLESCENT; ADULT; AGED; AXONS; CHARCOT-MARIE-TOOTH DISEASE; CHILD; CHILD, PRESCHOOL; DISEASE PROGRESSION; HUMANS; MIDDLE AGED; NEURAL CONDUCTION;

EID: 0033554366     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb08618.x     Document Type: Article

References (2)

1. HARDING, A.E. 1995. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteins. Brain 18; 809-818.
2. HOOGENJIJK, J.E., et al. 1994. Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype. Muscle Nerve 17: 85-90.