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Hilary J Vernon

Showing results (1-10 of 63) with videos related to

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JAMA Pediatrics|June 16, 2015
Inborn Errors of Metabolism: Advances in Diagnosis and TherapyHilary J Vernon
American Journal of Medical Genetics. Part A|June 24, 2021
Milestones in treatments for inborn errors of metabolism: Reflections on Where chemistry and medicine meetHilary J Vernon, Irini Manoli
Handbook of Clinical Neurology|June 13, 2018
Mitochondrial ataxiasHilary J Vernon, Laurence A Bindoff
Future Cardiology|June 16, 2023
Temporal evolution of the heart failure phenotype in Barth syndrome and treatment with elamipretideHani N Sabbah, Carolyn Taylor, Hilary J Vernon
Molecular Genetics and Metabolism|April 23, 2014
Clinical laboratory studies in Barth SyndromeHilary J Vernon, Yana Sandlers, Rebecca McClellan, et al.
Molecular Genetics and Metabolism|August 7, 2023
FGF21 and GDF15 are elevated in Barth Syndrome and are correlated to important clinical measuresOlivia Liu, Bhargava Kumar Chinni, Cedric Manlhiot, et al.
American Journal of Medical Genetics. Part A|April 9, 2015
Mutations in FARS2 and non-fatal mitochondrial dysfunction in two siblingsHilary J Vernon, Rebecca McClellan, Denise A S Batista, et al.
Molecular Genetics and Metabolism Reports|June 10, 2020
<i>PARS2</i>-associated mitochondrial disease: A case report of a patient with prolonged survival and literature reviewMohammed A Almuqbil, Hilary J Vernon, Marcia Ferguson, et al.
European Heart Journal|July 24, 2025
Mitochondrial cardiomyopathies: pathogenesis, diagnosis, and treatmentChristoph Maack, Jan Dudek, Edoardo Bertero, et al.
Disease Models & Mechanisms|November 23, 2023
Inborn errors of amino acid metabolism - from underlying pathophysiology to therapeutic advancesShira G Ziegler, Jiyoung Kim, Jeffrey T Ehmsen, et al.
Pageof 7

Showing results (1-10 of 63) with videos related to

Sort By:
Pageof 7
JAMA Pediatrics|June 16, 2015
Inborn Errors of Metabolism: Advances in Diagnosis and TherapyHilary J Vernon
American Journal of Medical Genetics. Part A|June 24, 2021
Milestones in treatments for inborn errors of metabolism: Reflections on Where chemistry and medicine meetHilary J Vernon, Irini Manoli
Handbook of Clinical Neurology|June 13, 2018
Mitochondrial ataxiasHilary J Vernon, Laurence A Bindoff
Future Cardiology|June 16, 2023
Temporal evolution of the heart failure phenotype in Barth syndrome and treatment with elamipretideHani N Sabbah, Carolyn Taylor, Hilary J Vernon
Molecular Genetics and Metabolism|April 23, 2014
Clinical laboratory studies in Barth SyndromeHilary J Vernon, Yana Sandlers, Rebecca McClellan, et al.
Molecular Genetics and Metabolism|August 7, 2023
FGF21 and GDF15 are elevated in Barth Syndrome and are correlated to important clinical measuresOlivia Liu, Bhargava Kumar Chinni, Cedric Manlhiot, et al.
American Journal of Medical Genetics. Part A|April 9, 2015
Mutations in FARS2 and non-fatal mitochondrial dysfunction in two siblingsHilary J Vernon, Rebecca McClellan, Denise A S Batista, et al.
Molecular Genetics and Metabolism Reports|June 10, 2020
<i>PARS2</i>-associated mitochondrial disease: A case report of a patient with prolonged survival and literature reviewMohammed A Almuqbil, Hilary J Vernon, Marcia Ferguson, et al.
European Heart Journal|July 24, 2025
Mitochondrial cardiomyopathies: pathogenesis, diagnosis, and treatmentChristoph Maack, Jan Dudek, Edoardo Bertero, et al.
Disease Models & Mechanisms|November 23, 2023
Inborn errors of amino acid metabolism - from underlying pathophysiology to therapeutic advancesShira G Ziegler, Jiyoung Kim, Jeffrey T Ehmsen, et al.
Pageof 7