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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 mutation
M 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 Turkey
B 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 study
J Kirschner, D Schorling, D Hauschke, et al.
Neurology
|
July 21, 2006
GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis
S Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu, A Adami, et al.
Page
of 4
Search research articles
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Showing results (31-40 of 34) with videos related to
Sort By:
Page
of 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 mutation
M 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 Turkey
B 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 study
J Kirschner, D Schorling, D Hauschke, et al.
Neurology
|
July 21, 2006
GAMT deficiency: features, treatment, and outcome in an inborn error of creatine synthesis
S Mercimek-Mahmutoglu, S Stoeckler-Ipsiroglu, A Adami, et al.
Page
of 4