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Catarina M Quinzii

Showing results (1-10 of 65) with videos related to

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Developmental Disabilities Research Reviews|September 7, 2010
Coenzyme Q and mitochondrial diseaseCatarina M Quinzii, Michio Hirano
Journal of Translational Genetics and Genomics|January 11, 2021
Redefining infantile-onset multisystem phenotypes of coenzyme Q<sub>10</sub>-deficiency in the next-generation sequencing eraAndres Berardo, Catarina M Quinzii
Biofactors (Oxford, England)|October 13, 2011
Primary and secondary CoQ(10) deficiencies in humansCatarina M Quinzii, Michio Hirano
JAMA Neurology|July 2, 2016
Coenzyme Q10 as a Peripheral Biomarker for Multiple System AtrophySheng-Han Kuo, Catarina M Quinzii
Journal of Advanced Research|December 15, 2020
Abnormalities of hydrogen sulfide and glutathione pathways in mitochondrial dysfunctionCatarina M Quinzii, Luis C Lopez
The New England Journal of Medicine|July 3, 2014
Mutant COQ2 in multiple-system atrophyCatarina M Quinzii, Michio Hirano, Salvatore DiMauro
Biochimica Et Biophysica Acta|January 26, 2012
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disordersMichio Hirano, Caterina Garone, Catarina M Quinzii
Neurochemical Research|November 10, 2006
Human coenzyme Q10 deficiencyCatarina M Quinzii, Salvatore DiMauro, Michio Hirano
The Journal of Clinical Investigation|March 3, 2007
Mutations in coenzyme Q10 biosynthetic genesSalvatore DiMauro, Catarina M Quinzii, Michio Hirano
Journal of Neurological Disorders & Stroke|August 16, 2014
Cerebellar Ataxia and <i>CoQ10</i> DeficiencyCatarina M Quinzii, Michio Hirano, Ali Naini
Pageof 7

Showing results (1-10 of 65) with videos related to

Sort By:
Pageof 7
Developmental Disabilities Research Reviews|September 7, 2010
Coenzyme Q and mitochondrial diseaseCatarina M Quinzii, Michio Hirano
Journal of Translational Genetics and Genomics|January 11, 2021
Redefining infantile-onset multisystem phenotypes of coenzyme Q<sub>10</sub>-deficiency in the next-generation sequencing eraAndres Berardo, Catarina M Quinzii
Biofactors (Oxford, England)|October 13, 2011
Primary and secondary CoQ(10) deficiencies in humansCatarina M Quinzii, Michio Hirano
JAMA Neurology|July 2, 2016
Coenzyme Q10 as a Peripheral Biomarker for Multiple System AtrophySheng-Han Kuo, Catarina M Quinzii
Journal of Advanced Research|December 15, 2020
Abnormalities of hydrogen sulfide and glutathione pathways in mitochondrial dysfunctionCatarina M Quinzii, Luis C Lopez
The New England Journal of Medicine|July 3, 2014
Mutant COQ2 in multiple-system atrophyCatarina M Quinzii, Michio Hirano, Salvatore DiMauro
Biochimica Et Biophysica Acta|January 26, 2012
CoQ(10) deficiencies and MNGIE: two treatable mitochondrial disordersMichio Hirano, Caterina Garone, Catarina M Quinzii
Neurochemical Research|November 10, 2006
Human coenzyme Q10 deficiencyCatarina M Quinzii, Salvatore DiMauro, Michio Hirano
The Journal of Clinical Investigation|March 3, 2007
Mutations in coenzyme Q10 biosynthetic genesSalvatore DiMauro, Catarina M Quinzii, Michio Hirano
Journal of Neurological Disorders & Stroke|August 16, 2014
Cerebellar Ataxia and <i>CoQ10</i> DeficiencyCatarina M Quinzii, Michio Hirano, Ali Naini
Pageof 7