Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular Dystrophy

Author:

Burch Peter M.1,Pogoryelova Oksana2,Goldstein Richard1,Bennett Donald3,Guglieri Michela2,Straub Volker2,Bushby Kate2,Lochmüller Hanns2,Morris Carl3

Affiliation:

1. Worldwide Research & Development, Pfizer Inc., Groton, CT, USA

2. John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK

3. Worldwide Research & Development, Pfizer Inc., Cambridge, MA, USA

Publisher

IOS Press

Subject

Neurology (clinical),Neurology

Reference40 articles.

1. The muscular dystrophies;Flanigan;Seminars in Neurology,2012

2. Evidence-based path to newborn screening for Duchenne muscular dystrophy;Mendell;Annals of Neurology,2012

3. Challenges in Duchenne muscular dystrophy;Davies;Neuromuscular disorders: NMD,1997

4. Limb-girdle muscular dystrophies–from genetics to molecular pathology;Laval;Neuropathology and Applied Neurobiology,2004

5. Treatment of dysferlinopathy with deflazacort: A double-blind, placebo-controlled clinical trial;Walter;Orphanet Journal of Rare Diseases,2013

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