Charcot-Marie-Tooth disease type 1A with central nervous system involvement in two generations [5]

Journal of Neurology

Volumn 251, Issue 4, 2004, Pages 484-485

  Panas, M ^a   Karadima, G ^a   Kalfakis, N ^a   Floroskufi, P ^a   Vassilopoulos, D ^a  

^a NATIONAL AND KAPODISTRIAN UNIVERSITY OF ATHENS   (Greece)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANGIOGRAPHY; CASE REPORT; CENTRAL NERVOUS SYSTEM; CLINICAL EXAMINATION; CLINICAL FEATURE; ELECTROPHYSIOLOGY; FEMALE; GAIT; HEREDITARY MOTOR SENSORY NEUROPATHY; HEREDITY; HUMAN; LETTER; MALE; MEDICAL RECORD; MOTOR NERVE CONDUCTION; MYELIN SHEATH; NUCLEAR MAGNETIC RESONANCE IMAGING; PHENOTYPIC VARIATION; PHYSICAL EXAMINATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROGENY; TRANSCRANIAL MAGNETIC STIMULATION;

ADULT; CENTRAL NERVOUS SYSTEM DISEASES; CHARCOT-MARIE-TOOTH DISEASE; FAMILY CHARACTERISTICS; FEMALE; HUMANS; MALE; MIDDLE AGED;

EID: 16544362807     PISSN: 03405354     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00415-004-0376-5     Document Type: Letter

References (11)

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