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Ali Naini

Showing results (21-30 of 52) with videos related to

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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|April 25, 2003
A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosisMichelangelo Mancuso, Massimiliano Filosto, Ali Naini, et al.
Journal of Child Neurology|October 5, 2012
Diabetic Ketoacidosis in an Adult Patient With Spinal Muscular Atrophy Type II: Further Evidence of Extraneural Pathology Due to Survival Motor Neuron 1 Mutation?Nicole Holuba Lamarca, Lauren Golden, Rita Marie John, et al.
Journal of Child Neurology|September 22, 2016
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement DisorderCaterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, 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.
Mitochondrion|August 27, 2005
Mitochondrial neurogastrointestinal encephalomyopathy and thymidine metabolism: results and hypothesesRamon Marti, Antonella Spinazzola, Ichizo Nishino, 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.
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Plos One|August 7, 2010
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effectsLuis C López, Catarina M Quinzii, Estela Area, et al.
American Journal of Human Genetics|December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsLuis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosisSara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
Pageof 6

Showing results (21-30 of 52) with videos related to

Sort By:
Pageof 6
Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|April 25, 2003
A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosisMichelangelo Mancuso, Massimiliano Filosto, Ali Naini, et al.
Journal of Child Neurology|October 5, 2012
Diabetic Ketoacidosis in an Adult Patient With Spinal Muscular Atrophy Type II: Further Evidence of Extraneural Pathology Due to Survival Motor Neuron 1 Mutation?Nicole Holuba Lamarca, Lauren Golden, Rita Marie John, et al.
Journal of Child Neurology|September 22, 2016
A Novel SUCLA2 Mutation Presenting as a Complex Childhood Movement DisorderCaterina Garone, Juliana Gurgel-Giannetti, Simone Sanna-Cherchi, 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.
Mitochondrion|August 27, 2005
Mitochondrial neurogastrointestinal encephalomyopathy and thymidine metabolism: results and hypothesesRamon Marti, Antonella Spinazzola, Ichizo Nishino, 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.
Archives of Neurology|September 12, 2012
MPV17 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsCaterina Garone, Juan Carlos Rubio, Sarah E Calvo, et al.
Plos One|August 7, 2010
Treatment of CoQ(10) deficient fibroblasts with ubiquinone, CoQ analogs, and vitamin C: time- and compound-dependent effectsLuis C López, Catarina M Quinzii, Estela Area, et al.
American Journal of Human Genetics|December 23, 2006
Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutationsLuis Carlos López, Markus Schuelke, Catarina M Quinzii, et al.
American Journal of Medical Genetics. Part A|September 17, 2004
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosisSara Shanske, Jacklyn Pancrudo, Petra Kaufmann, et al.
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