A clinical approach to muscle diseases

Seminars in Neurology

Volumn 28, Issue 2, 2008, Pages 228-240

  Jackson, Carlayne E ^a,b  

^a UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER AT SAN ANTONIO   (United States)

^b University of Texas Health Science Center   (United States)

Author keywords

Cardiomyopathy; Creatine kinase; Myalgia; Myoglobinuria; Myopathy; Myotonia

Indexed keywords

CREATINE KINASE;

BLOOD SAMPLING; CLINICAL EVALUATION; CREATINE KINASE BLOOD LEVEL; DIFFERENTIAL DIAGNOSIS; ELECTROPHYSIOLOGY; FAMILY HISTORY; HEART DISEASE; HEREDITARY SPINAL MUSCULAR ATROPHY; HUMAN; LABORATORY TEST; MOLECULAR GENETICS; MUSCLE BIOPSY; MUSCLE CONTRACTURE; MUSCLE DISEASE; MYOGLOBINURIA; MYOPATHY; MYOTONIA; PHENOTYPE; PRIORITY JOURNAL; PTOSIS; RESPIRATORY FAILURE; REVIEW; SYMPTOMATOLOGY;

CREATINE KINASE; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MUSCLE WEAKNESS; MUSCLE, SKELETAL; MUSCULAR DISEASES; MYOPATHIES, STRUCTURAL, CONGENITAL; NEUROLOGIC EXAMINATION;

EID: 41149110780     PISSN: 02718235     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1062266     Document Type: Review

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