Literature DB >> 22239869

Use of skeletal muscle MRI in diagnosis and monitoring disease progression in Duchenne muscular dystrophy.

Erika L Finanger1, Barry Russman, Sean C Forbes, William D Rooney, Glenn A Walter, Krista Vandenborne.   

Abstract

Studies have shown promise in using various approaches of magnetic resonance imaging (MRI) and magnetic resonance spectroscopy to evaluate skeletal muscle involvement in Duchenne muscular dystrophy. However, these studies have mainly been performed using a cross-sectional design, and the correlation of these MRI changes with disease progression and disease severity has not been fully elucidated. Overall, skeletal muscle MRI is a powerful and sensitive technique in the evaluation of muscle disease, and its use as a biomarker for disease progression or therapeutic response in clinical trials deserves further study.
Copyright © 2012. Published by Elsevier Inc.

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Year:  2011        PMID: 22239869      PMCID: PMC3561672          DOI: 10.1016/j.pmr.2011.11.004

Source DB:  PubMed          Journal:  Phys Med Rehabil Clin N Am        ISSN: 1047-9651            Impact factor:   1.784


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  29 in total

1.  Patterns of decline in upper limb function of boys and men with DMD: an international survey.

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Authors:  Jordi Díaz-Manera; Jaume Llauger; Eduard Gallardo; Isabel Illa
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Authors:  William D Rooney; Yosef A Berlow; William T Triplett; Sean C Forbes; Rebecca J Willcocks; Dah-Jyuu Wang; Ishu Arpan; Harneet Arora; Claudia Senesac; Donovan J Lott; Gihan Tennekoon; Richard Finkel; Barry S Russman; Erika L Finanger; Saptarshi Chakraborty; Elliott O'Brien; Brendan Moloney; Alison Barnard; H Lee Sweeney; Michael J Daniels; Glenn A Walter; Krista Vandenborne
Journal:  Neurology       Date:  2020-03-17       Impact factor: 9.910

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Authors:  Skorn Ponrartana; Leigh Ramos-Platt; Tishya Anne Leong Wren; Houchun Harry Hu; Thomas Gardner Perkins; Jonathan Mawlin Chia; Vicente Gilsanz
Journal:  Pediatr Radiol       Date:  2014-09-23
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