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Georgirene D Vladutiu

Showing results (1-10 of 32) with videos related to

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Current Opinion in Rheumatology|October 24, 2008
Genetic predisposition to statin myopathyGeorgirene D Vladutiu
Muscle & Nerve|May 8, 2002
Laboratory diagnosis of metabolic myopathiesGeorgirene D Vladutiu
Muscle & Nerve|June 29, 2004
Association of medically unexplained fatigue with ACE insertion/deletion polymorphism in Gulf War veteransGeorgirene D Vladutiu, Benjamin H Natelson
Anesthesia and Analgesia|September 19, 2009
Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutationKirk J Hogan, Georgirene D Vladutiu
Molecular Genetics and Metabolism|June 28, 2005
A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle diseasePaul J Isackson, Mark Tarnopolsky, Georgirene D Vladutiu
Molecular Genetics and Metabolism|September 26, 2006
Identification of 16 new disease-causing mutations in the CPT2 gene resulting in carnitine palmitoyltransferase II deficiencyPaul J Isackson, Michael J Bennett, Georgirene D Vladutiu
Molecular Genetics and Metabolism|July 26, 2005
Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 genePaul J Isackson, Heather Bujnicki, Cary O Harding, et al.
Journal of Neuromuscular Diseases|March 9, 2017
Histopathologic and Biochemical Evidence for Mitochondrial Disease Among 279 Patients with Severe Statin MyopathyTieying Hou, Yilan Li, Weiwei Chen, et al.
Muscle & Nerve|November 22, 2012
Novel mutations in the gene encoding very long-chain acyl-CoA dehydrogenase identified in patients with partial carnitine palmitoyltransferase II deficiencyPaul J Isackson, Kristin A Sutton, Karl Y Hostetler, et al.
AJNR. American Journal of Neuroradiology|August 11, 2005
Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defectsFernando Scaglia, Lee-Jun C Wong, Georgirene D Vladutiu, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Current Opinion in Rheumatology|October 24, 2008
Genetic predisposition to statin myopathyGeorgirene D Vladutiu
Muscle & Nerve|May 8, 2002
Laboratory diagnosis of metabolic myopathiesGeorgirene D Vladutiu
Muscle & Nerve|June 29, 2004
Association of medically unexplained fatigue with ACE insertion/deletion polymorphism in Gulf War veteransGeorgirene D Vladutiu, Benjamin H Natelson
Anesthesia and Analgesia|September 19, 2009
Malignant hyperthermia-like syndrome and carnitine palmitoyltransferase II deficiency with heterozygous R503C mutationKirk J Hogan, Georgirene D Vladutiu
Molecular Genetics and Metabolism|June 28, 2005
A novel mutation in the PYGM gene in a family with pseudo-dominant transmission of McArdle diseasePaul J Isackson, Mark Tarnopolsky, Georgirene D Vladutiu
Molecular Genetics and Metabolism|September 26, 2006
Identification of 16 new disease-causing mutations in the CPT2 gene resulting in carnitine palmitoyltransferase II deficiencyPaul J Isackson, Michael J Bennett, Georgirene D Vladutiu
Molecular Genetics and Metabolism|July 26, 2005
Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 genePaul J Isackson, Heather Bujnicki, Cary O Harding, et al.
Journal of Neuromuscular Diseases|March 9, 2017
Histopathologic and Biochemical Evidence for Mitochondrial Disease Among 279 Patients with Severe Statin MyopathyTieying Hou, Yilan Li, Weiwei Chen, et al.
Muscle & Nerve|November 22, 2012
Novel mutations in the gene encoding very long-chain acyl-CoA dehydrogenase identified in patients with partial carnitine palmitoyltransferase II deficiencyPaul J Isackson, Kristin A Sutton, Karl Y Hostetler, et al.
AJNR. American Journal of Neuroradiology|August 11, 2005
Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defectsFernando Scaglia, Lee-Jun C Wong, Georgirene D Vladutiu, et al.
Pageof 4