Literature DB >> 1747144

Serial magnetic resonance imaging in juvenile dermatomyositis.

D R Keim1, R J Hernandez, D B Sullivan.   

Abstract

Magnetic resonance imaging (MRI) was used to follow the course of juvenile dermatomyositis from the onset of disease through resolution of a primary relapse. The signal intensity of the T2-weighted image of involved muscles was elevated during periods of disease activity, and returned to approximately normal levels with effective suppression of disease activity. T1-weighted images of involved muscles remained approximately normal despite disease activity.

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Year:  1991        PMID: 1747144     DOI: 10.1002/art.1780341217

Source DB:  PubMed          Journal:  Arthritis Rheum        ISSN: 0004-3591


  5 in total

Review 1.  Imaging of muscle disorders in children.

Authors:  Karl Johnson; Penny J C Davis; J Katharine Foster; Janet E McDonagh; Clive A J Ryder; Taunton R Southwood
Journal:  Pediatr Radiol       Date:  2006-06-15

2.  Serial magnetic resonance imaging in juvenile dermatomyositis--delayed normalization.

Authors:  H I Huppertz; W A Kaiser
Journal:  Rheumatol Int       Date:  1994       Impact factor: 2.631

3.  Muscle MRI at the time of questionable disease flares in Juvenile Dermatomyositis (JDM).

Authors:  Rabheh Abdul-Aziz; Chack-Yung Yu; Brent Adler; Sharon Bout-Tabaku; Katherine E Lintner; Melissa Moore-Clingenpeel; Charles H Spencer
Journal:  Pediatr Rheumatol Online J       Date:  2017-04-12       Impact factor: 3.054

4.  Fashionably Late: A Case of Delayed Cutaneous Manifestations in Juvenile Dermatomyositis.

Authors:  Maya Antoine; Patrick T Reeves; Luis Rohena; Olcay Jones; Brian Faux
Journal:  J Clin Med Res       Date:  2018-10-09

Review 5.  MRI and muscle imaging for idiopathic inflammatory myopathies.

Authors:  Samuel Malartre; Damien Bachasson; Guillaume Mercy; Elissone Sarkis; Céline Anquetil; Olivier Benveniste; Yves Allenbach
Journal:  Brain Pathol       Date:  2021-05       Impact factor: 6.508

  5 in total

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