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Volumn 23, Issue 3, 2012, Pages 495-563

Clinical approach to the diagnostic evaluation of hereditary and acquired neuromuscular diseases

Author keywords

Diagnostic evaluation; History; Motor neuron disease; Myopathy; Neuromuscular disease; Neuromuscular junction; Neuropathy; Physical examination

Indexed keywords

ACQUIRED NEUROMUSCULAR DISEASE; ANAMNESIS; ANTERIOR HORN CELL DISEASE; CLINICAL FEATURE; DIAGNOSTIC TEST; EARLY DIAGNOSIS; ELECTROMYOGRAM; FAMILY HISTORY; FUNCTIONAL ASSESSMENT; GENETIC DISORDER; HEALTH CARE COST; HEREDITARY NEUROMUSCULAR DISEASE; HISTOPATHOLOGY; HUMAN; LABORATORY TEST; MOLECULAR GENETICS; MOTOR NEURON DISEASE; MUSCLE BIOPSY; MUSCLE DISEASE; MUSCULOSKELETAL SYSTEM; NERVE BIOPSY; NERVE CONDUCTION; NEUROLOGIC EXAMINATION; NEUROMUSCULAR DISEASE; NEUROMUSCULAR JUNCTION DISORDER; PERIPHERAL NEUROPATHY; PHYSICAL EXAMINATION; PRIORITY JOURNAL; REVIEW; SECONDARY PREVENTION; SENSITIVITY AND SPECIFICITY;

EID: 84865560619     PISSN: 10479651     EISSN: 15581381     Source Type: Journal    
DOI: 10.1016/j.pmr.2012.06.011     Document Type: Review
Times cited : (85)

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