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Hasan O Akman

Showing results (1-10 of 31) with videos related to

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Human Molecular Genetics|October 14, 2010
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensationBeatriz Dorado, Estela Area, Hasan O Akman, et al.
Archives of Neurology|March 11, 2009
Muscle phosphoglycerate mutase deficiency revisitedAli 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 considerationsRonen 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 DNAJacklyn 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 literatureRebecca J Levy, Purificación Gutierrez Ríos, Hasan O Akman, et al.
Neuromuscular Disorders : NMD|January 19, 2010
Muscle phosphorylase b kinase deficiency revisitedAndoni 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 biopsySara Shanske, Ali Naini, Ramen H Chmait, et al.
Blood|November 2, 2002
Cellular response to hypoxia involves signaling via Smad proteinsHong Zhang, Hasan O Akman, Eric L P Smith, et al.
Genomics|March 25, 2008
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosisMolly 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 graftsSadi Kaplan, Jeffrey A Morgan, Gianluigi Bisleri, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|October 14, 2010
Onset and organ specificity of Tk2 deficiency depends on Tk1 down-regulation and transcriptional compensationBeatriz Dorado, Estela Area, Hasan O Akman, et al.
Archives of Neurology|March 11, 2009
Muscle phosphoglycerate mutase deficiency revisitedAli 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 considerationsRonen 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 DNAJacklyn 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 literatureRebecca J Levy, Purificación Gutierrez Ríos, Hasan O Akman, et al.
Neuromuscular Disorders : NMD|January 19, 2010
Muscle phosphorylase b kinase deficiency revisitedAndoni 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 biopsySara Shanske, Ali Naini, Ramen H Chmait, et al.
Blood|November 2, 2002
Cellular response to hypoxia involves signaling via Smad proteinsHong Zhang, Hasan O Akman, Eric L P Smith, et al.
Genomics|March 25, 2008
Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosisMolly 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 graftsSadi Kaplan, Jeffrey A Morgan, Gianluigi Bisleri, et al.
Pageof 4