Muscle sonography in six patients with hereditary inclusion body myopathy

Skeletal Radiology

Volumn 37, Issue 1, 2008, Pages 43-48

  Adler, Ronald S ^a   Garolfalo, Giovanna ^b   Paget, Stephen ^a   Kagen, Lawrence ^a  

^a WEILL CORNELL MEDICAL COLLEGE   (United States)

^b Ospedale Residenza Sanitaria Riabilitativa   (Italy)

Author keywords

Genetic mutation; Inclusion body; Myopathy; Sonography; Target sign

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; DOPPLER ECHOGRAPHY; FEMALE; FOLLOW UP; GENE MUTATION; HAMSTRING; HEREDITARY INCLUSION BODY MYOPATHY; HOMOZYGOSITY; HUMAN; IRAN; JEW; MALE; MUSCLE; MUSCLE ATROPHY; MUSCLE BLOOD FLOW; MUSCLE BLOOD VESSEL; MYOPATHY; PRIORITY JOURNAL; QUADRICEPS FEMORIS MUSCLE; RECTUS FEMORIS MUSCLE;

ADULT; COHORT STUDIES; DISEASE PROGRESSION; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MIDDLE AGED; MUSCLE, SKELETAL; MUSCULAR ATROPHY; MYOSITIS, INCLUSION BODY; OBSERVER VARIATION; SEVERITY OF ILLNESS INDEX; ULTRASONOGRAPHY, DOPPLER;

EID: 36349012566     PISSN: 03642348     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00256-007-0367-6     Document Type: Article

References (10)

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