Neuromuscular imaging in inherited muscle diseases

European Radiology

Volumn 20, Issue 10, 2010, Pages 2447-2460

  Wattjes, Mike P ^d   Kley, Rudolf A ^a   Fischer, Dirk ^b,c  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b UNIVERSITY HOSPITAL BASEL   (Switzerland)

^c UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^d NONE

Author keywords

Congenital myopathy; Inherited muscle diseases; Limb girdle muscular dystrophy; Muscle MRI; Muscular dystrophy; Myotonic dystrophy

Indexed keywords

ALPHA CRYSTALLIN; ALPHA SARCOGLYCAN; CALPAIN 3; CONTRAST MEDIUM; DESMIN; DYSFERLIN; FUKUTIN RELATED PROTEIN; SARCOGLYCAN;

ALGORITHM; ARTICLE; BECKER MUSCULAR DYSTROPHY; CALPAINOPATHY; CLINICAL FEATURE; CLINICAL PROTOCOL; COMPUTER ASSISTED TOMOGRAPHY; DIAGNOSTIC IMAGING; DISEASE SEVERITY; DUCHENNE MUSCULAR DYSTROPHY; DYSFERLINOPATHY; DYSTROPHY; GENE MUTATION; GENETIC DISORDER; HEREDITARY MUSCLE DISEASE; HUMAN; INTERMETHOD COMPARISON; LIMB GIRDLE MUSCULAR DYSTROPHY; METABOLIC MYELOPATHY; MUSCLE BIOPSY; MUSCLE DISEASE; MUSCULAR DYSTROPHY; MYOFIBRILLAR MYOPATHY; MYOPATHY; NEUROMUSCULAR DISEASE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN DEFICIENCY; RADIATION DOSE; SARCOGLYCAN DEFICIENCY; SEDATION; SENSITIVITY ANALYSIS; ULTRASOUND;

ADOLESCENT; ADULT; CALPAIN; DIAGNOSTIC IMAGING; FEMALE; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MEMBRANE PROTEINS; MUSCLE PROTEINS; MUSCLES; MUSCULAR DISEASES; MUSCULAR DYSTROPHIES, LIMB-GIRDLE; SARCOGLYCANS; TOMOGRAPHY, X-RAY COMPUTED;

EID: 77957860016     PISSN: 09387994     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00330-010-1799-2     Document Type: Article

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