Literature DB >> 6410854

CT of primary muscle diseases.

M Jiddane, J L Gastaut, J F Pellissier, J Pouget, G Serratrice, G Salamon.   

Abstract

Seventy-five patients with a variety of muscular dystrophies were studied using computed tomography (CT). At least 11 slices were taken in each patient, from the forearm to the lower leg. Sufficient information was obtained to provide some CT characteristics of several dystrophies, including Duchenne muscular dystrophy, facioscapulohumeral syndrome, limb-girdle muscle myopathies, and myopathic dystrophies. CT promises to be of increasing value in these areas in the future.

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Year:  1983        PMID: 6410854      PMCID: PMC8334900     

Source DB:  PubMed          Journal:  AJNR Am J Neuroradiol        ISSN: 0195-6108            Impact factor:   3.825


  3 in total

1.  Whole-body MR screening of muscles in the evaluation of neuromuscular diseases.

Authors:  O Ozsarlak; P M Parizel; A M De Schepper; P De Jonghe; J J Martin
Journal:  Eur Radiol       Date:  2004-03-09       Impact factor: 5.315

2.  CT muscle scanning in the evaluation of patients with spinal muscular atrophy (SMA).

Authors:  P Sambrook; D Rickards; W J Cumming
Journal:  Neuroradiology       Date:  1988       Impact factor: 2.804

3.  Magnetic resonance imaging of children with Duchenne muscular dystrophy.

Authors:  A Schreiber; W L Smith; V Ionasescu; H Zellweger; E A Franken; V Dunn; J Ehrhardt
Journal:  Pediatr Radiol       Date:  1987
  3 in total

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