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Human Molecular Genetics
|
October 14, 2010
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensation
Beatriz Dorado, Estela Area, Hasan O Akman, et al.
Archives of Neurology
|
March 11, 2009
Muscle phosphoglycerate mutase deficiency revisited
Ali Naini, Antonio Toscano, Olimpia Musumeci, et al.
Neuromuscular Disorders : NMD
|
January 23, 2009
Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerations
Ronen Spiegel, Estela Area Gomez, Hasan O Akman, et al.
Journal of Child Neurology
|
August 24, 2007
Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA
Jacklyn Pancrudo, Sara Shanske, Eduardo Bonilla, et al.
Journal of Child Neurology
|
November 29, 2013
Long survival in patients with leigh syndrome and the m.10191T>C mutation in MT-ND3 : a case report and review of the literature
Rebecca J Levy, Purificación Gutierrez Ríos, Hasan O Akman, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Muscle phosphorylase b kinase deficiency revisited
Andoni Echaniz-Laguna, Hasan O Akman, Michel Mohr, et al.
Journal of Child Neurology
|
April 26, 2012
Mutation in an mtDNA protein-coding gene: prenatal diagnosis aided by fetal muscle biopsy
Sara Shanske, Ali Naini, Ramen H Chmait, et al.
Blood
|
November 2, 2002
Cellular response to hypoxia involves signaling via Smad proteins
Hong Zhang, Hasan O Akman, Eric L P Smith, et al.
Genomics
|
March 25, 2008
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis
Molly E McCue, Stephanie J Valberg, Michael B Miller, et al.
The Annals of Thoracic Surgery
|
October 26, 2005
Effects of resveratrol in storage solution on adhesion molecule expression and nitric oxide synthesis in vein grafts
Sadi Kaplan, Jeffrey A Morgan, Gianluigi Bisleri, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 31) with videos related to
Sort By:
Page
of 4
Human Molecular Genetics
|
October 14, 2010
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensation
Beatriz Dorado, Estela Area, Hasan O Akman, et al.
Archives of Neurology
|
March 11, 2009
Muscle phosphoglycerate mutase deficiency revisited
Ali Naini, Antonio Toscano, Olimpia Musumeci, et al.
Neuromuscular Disorders : NMD
|
January 23, 2009
Myopathic form of phosphoglycerate kinase (PGK) deficiency: a new case and pathogenic considerations
Ronen Spiegel, Estela Area Gomez, Hasan O Akman, et al.
Journal of Child Neurology
|
August 24, 2007
Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA
Jacklyn Pancrudo, Sara Shanske, Eduardo Bonilla, et al.
Journal of Child Neurology
|
November 29, 2013
Long survival in patients with leigh syndrome and the m.10191T>C mutation in MT-ND3 : a case report and review of the literature
Rebecca J Levy, Purificación Gutierrez Ríos, Hasan O Akman, et al.
Neuromuscular Disorders : NMD
|
January 19, 2010
Muscle phosphorylase b kinase deficiency revisited
Andoni Echaniz-Laguna, Hasan O Akman, Michel Mohr, et al.
Journal of Child Neurology
|
April 26, 2012
Mutation in an mtDNA protein-coding gene: prenatal diagnosis aided by fetal muscle biopsy
Sara Shanske, Ali Naini, Ramen H Chmait, et al.
Blood
|
November 2, 2002
Cellular response to hypoxia involves signaling via Smad proteins
Hong Zhang, Hasan O Akman, Eric L P Smith, et al.
Genomics
|
March 25, 2008
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis
Molly E McCue, Stephanie J Valberg, Michael B Miller, et al.
The Annals of Thoracic Surgery
|
October 26, 2005
Effects of resveratrol in storage solution on adhesion molecule expression and nitric oxide synthesis in vein grafts
Sadi Kaplan, Jeffrey A Morgan, Gianluigi Bisleri, et al.
Page
of 4