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Sara Shanske

Showing results (11-20 of 45) with videos related to

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Journal of the Neurological Sciences|March 12, 2005
Hypocitrullinemia in patients with MELAS: an insight into the "MELAS paradox"Ali Naini, Petra Kaufmann, Sara Shanske, et al.
Archives of Neurology|October 22, 2003
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genesMichelangelo Mancuso, Massimiliano Filosto, Seiichi Tsujino, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 30, 2005
Achalasia as the harbinger of a novel mitochondrial disorder in childhoodGisela Chelimsky, Sara Shanske, Michio Hirano, et al.
Muscle & Nerve|December 2, 2005
Benign course of glycogen storage disease type IIb in two brothers: nature or nurture?Alfred E Slonim, Linda Bulone, Jennifer Minikes, 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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2008
Mitochondrial dysfunction in mut methylmalonic acidemiaRandy J Chandler, Patricia M Zerfas, Sara Shanske, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Mitochondrial myopathy associated with a novel mutation in mtDNAJacklyn Pancrudo, Sara Shanske, Jorida Coku, 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.
Journal of the Neurological Sciences|December 22, 2009
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) geneJorida Coku, Sara Shanske, Mahsa Mehrazin, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
A 14-year-old male with asymptomatic proteinuria and hearing lossSamih H Nasr, Howard Corey, Sara Shanske, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Journal of the Neurological Sciences|March 12, 2005
Hypocitrullinemia in patients with MELAS: an insight into the "MELAS paradox"Ali Naini, Petra Kaufmann, Sara Shanske, et al.
Archives of Neurology|October 22, 2003
Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genesMichelangelo Mancuso, Massimiliano Filosto, Seiichi Tsujino, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 30, 2005
Achalasia as the harbinger of a novel mitochondrial disorder in childhoodGisela Chelimsky, Sara Shanske, Michio Hirano, et al.
Muscle & Nerve|December 2, 2005
Benign course of glycogen storage disease type IIb in two brothers: nature or nurture?Alfred E Slonim, Linda Bulone, Jennifer Minikes, 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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 18, 2008
Mitochondrial dysfunction in mut methylmalonic acidemiaRandy J Chandler, Patricia M Zerfas, Sara Shanske, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Mitochondrial myopathy associated with a novel mutation in mtDNAJacklyn Pancrudo, Sara Shanske, Jorida Coku, 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.
Journal of the Neurological Sciences|December 22, 2009
Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA(Leu(CUN)) geneJorida Coku, Sara Shanske, Mahsa Mehrazin, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
A 14-year-old male with asymptomatic proteinuria and hearing lossSamih H Nasr, Howard Corey, Sara Shanske, et al.
Pageof 5