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Sara Seneca

Showing results (31-40 of 88) with videos related to

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Archives of Neurology|September 12, 2007
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathyAnn Meulemans, Boel De Paepe, Jan De Bleecker, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in <i>TK2</i> geneGeorge K Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, et al.
Mitochondrion|June 24, 2014
Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 geneFrançois-Guillaume Debray, Sara Seneca, Michel Gonce, et al.
Molecular Genetics and Metabolism|May 29, 2016
Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patientsJoseph P Dewulf, Catherine Barrea, Marie-Françoise Vincent, et al.
Journal of Assisted Reproduction and Genetics|November 29, 2018
Rare genetic variants potentially involved in ovarian hyperstimulation syndromeKatrien Stouffs, Sari Daelemans, Samuel Santos-Ribeiro, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 13, 2006
A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalisAnn Meulemans, Sara Seneca, Joel Smet, et al.
Electrophoresis|October 29, 2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNAJoél Smet, Sara Seneca, Boel De Paepe, et al.
Journal of Assisted Reproduction and Genetics|March 12, 2010
The reproductive outcome of female patients with myotonic dystrophy type 1 (DM1) undergoing PGD is not affected by the size of the expanded CTG repeat tractWillem Verpoest, Sara Seneca, Marjan De Rademaeker, et al.
Cells|February 15, 2022
Clinical Heterogeneity in <i>MT-ATP6</i> Pathogenic Variants: Same Genotype-Different OnsetSara Capiau, Joél Smet, Boel De Paepe, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathySara Seneca, Nathalie Goemans, Rudy Van Coster, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Archives of Neurology|September 12, 2007
Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathyAnn Meulemans, Boel De Paepe, Jan De Bleecker, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|September 9, 2020
Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in <i>TK2</i> geneGeorge K Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, et al.
Mitochondrion|June 24, 2014
Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 geneFrançois-Guillaume Debray, Sara Seneca, Michel Gonce, et al.
Molecular Genetics and Metabolism|May 29, 2016
Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patientsJoseph P Dewulf, Catherine Barrea, Marie-Françoise Vincent, et al.
Journal of Assisted Reproduction and Genetics|November 29, 2018
Rare genetic variants potentially involved in ovarian hyperstimulation syndromeKatrien Stouffs, Sari Daelemans, Samuel Santos-Ribeiro, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 13, 2006
A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalisAnn Meulemans, Sara Seneca, Joel Smet, et al.
Electrophoresis|October 29, 2009
Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNAJoél Smet, Sara Seneca, Boel De Paepe, et al.
Journal of Assisted Reproduction and Genetics|March 12, 2010
The reproductive outcome of female patients with myotonic dystrophy type 1 (DM1) undergoing PGD is not affected by the size of the expanded CTG repeat tractWillem Verpoest, Sara Seneca, Marjan De Rademaeker, et al.
Cells|February 15, 2022
Clinical Heterogeneity in <i>MT-ATP6</i> Pathogenic Variants: Same Genotype-Different OnsetSara Capiau, Joél Smet, Boel De Paepe, et al.
American Journal of Medical Genetics. Part A|August 2, 2005
A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathySara Seneca, Nathalie Goemans, Rudy Van Coster, et al.
Pageof 9