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Volumn 261, Issue 4, 2014, Pages 675-685

Evolution of Charcot-Marie-Tooth disease type 1A duplication: A 2-year clinico-electrophysiological and lower-limb muscle MRI longitudinal study

Author keywords

Charcot Marie Tooth disease type 1A; CMTNS; Electrophysiology; Functional disability scale; Hand held dynamometry; MRI; Muscle edema; Muscle fatty atrophy; PMP22 duplication

Indexed keywords

ADOLESCENT; ADULT; AREFLEXIA; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; DISABILITY; DYNAMOMETRY; EDEMA; ELECTROPHYSIOLOGY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LEG MUSCLE; LIMB WEAKNESS; LONGITUDINAL STUDY; MALE; MUSCLE ACTION POTENTIAL; MUSCLE STRENGTH; NERVE CONDUCTION; NEUROLOGIC EXAMINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; WALKING DIFFICULTY; DISEASE COURSE; ELECTRODIAGNOSIS; INNERVATION; LEG; MIDDLE AGED; MYOTATIC REFLEX; PATHOLOGY; PATHOPHYSIOLOGY; SKELETAL MUSCLE; WALKING; YOUNG ADULT;

EID: 84898850671     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-014-7248-4     Document Type: Article
Times cited : (11)

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