EMG and nerve conduction studies in children with congenital muscular dystrophy

Muscle and Nerve

Volumn 29, Issue 2, 2004, Pages 292-299

  Quijano Roy, Susana ^a,b   Renault, Francis ^a   Romero, Norma ^c   Guicheney, Pascale ^c   Fardeau, Michel ^c   Estournet, Brigitte ^b  

^a ARMAND TROUSSEAU HOSPITAL   (France)

^b RAYMOND POINCARÉ HOSPITAL   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

Author keywords

Electrodiagnosis; Floppy infant syndrome; Myopathy; Neuropathy; Repetitive discharges

Indexed keywords

FUKUTIN RELATED PROTEIN; GENE PRODUCT; MEROSIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; COL6A2 GENE; DENERVATION; ELECTRIC CONDUCTIVITY; ELECTRODIAGNOSIS; ELECTROMYOGRAM; FEMALE; GENE; GENE MUTATION; HUMAN; HUMAN TISSUE; INFANT; INFANTILE HYPOTONIA; LAMA2 GENE; MALE; MOTOR NERVE CONDUCTION; MUSCULAR DYSTROPHY; MYOPATHY; NERVE CONDUCTION; NEUROPATHY; NEWBORN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SENSORY NERVE; SENSORY NERVE CONDUCTION;

CHILD; ELECTRIC STIMULATION; ELECTROMYOGRAPHY; FEMALE; HUMANS; MALE; MUSCULAR DYSTROPHIES; MUTATION; NEURAL CONDUCTION; RETROSPECTIVE STUDIES;

EID: 0842347675     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.10544     Document Type: Article

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