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E Wraige

Showing results (11-20 of 16) with videos related to

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The Cochrane Database of Systematic Reviews|January 27, 2007
Surgery for scoliosis in Duchenne muscular dystrophyD K L Cheuk, V Wong, E Wraige, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Interfamilial phenotypic heterogeneity in SMARD1S Joseph, S A Robb, S Mohammed, et al.
Clinical and Experimental Dermatology|October 1, 2013
Homozygous variegate porphyria presenting with developmental and language delay in childhoodV A E Pinder, S T Holden, C Deshpande, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomyH S Heng, M Lim, M Absoud, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
Neuromuscular Disorders : NMD|May 1, 2013
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysisN Dlamini, N C Voermans, S Lillis, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
The Cochrane Database of Systematic Reviews|January 27, 2007
Surgery for scoliosis in Duchenne muscular dystrophyD K L Cheuk, V Wong, E Wraige, et al.
Neuromuscular Disorders : NMD|January 23, 2009
Interfamilial phenotypic heterogeneity in SMARD1S Joseph, S A Robb, S Mohammed, et al.
Clinical and Experimental Dermatology|October 1, 2013
Homozygous variegate porphyria presenting with developmental and language delay in childhoodV A E Pinder, S T Holden, C Deshpande, et al.
Neuromuscular Disorders : NMD|November 19, 2013
Outcome of children with acetylcholine receptor (AChR) antibody positive juvenile myasthenia gravis following thymectomyH S Heng, M Lim, M Absoud, et al.
Journal of Neurology|February 22, 2019
The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutationsG J Knuiman, B Küsters, L Eshuis, et al.
Neuromuscular Disorders : NMD|May 1, 2013
Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysisN Dlamini, N C Voermans, S Lillis, et al.
Pageof 2