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E Wilichowski

Showing results (31-40 of 34) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutationM Deschauer, P F Chinnery, A M Schaefer, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycan gene mutations in TurkeyB Balci, E Wilichowski, G Haliloğlu, et al.
Neuromuscular Disorders : NMD|December 5, 2013
Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot studyJ Kirschner, D Schorling, D Hauschke, et al.
Neurology|July 21, 2006
GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesisS Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu, A Adami, et al.
Pageof 4

Showing results (31-40 of 34) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 34 results.
Journal of Neurology, Neurosurgery, and Psychiatry|July 20, 2004
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutationM Deschauer, P F Chinnery, A M Schaefer, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|June 9, 2005
Beta-sarcoglycan gene mutations in TurkeyB Balci, E Wilichowski, G Haliloğlu, et al.
Neuromuscular Disorders : NMD|December 5, 2013
Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot studyJ Kirschner, D Schorling, D Hauschke, et al.
Neurology|July 21, 2006
GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesisS Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu, A Adami, et al.
Pageof 4