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S Seneca

Showing results (41-50 of 60) with videos related to

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Journal of Clinical Pathology|February 3, 2009
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defectsB De Paepe, J Smet, M Lammens, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.
Genes & Diseases|October 6, 2025
Transcriptional profiling reveals glucose-dependent regulation of <i>COL13A1</i> mRNA in Pompe patients: Prospect for a novel disease mechanismS Uyttebroeck, D V Ngoc, R Osei, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex IIRudy Van Coster, S Seneca, J Smet, et al.
Molecular and Cellular Endocrinology|September 29, 2001
PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndromeK Sermon, S Seneca, M De Rycke, et al.
Clinical Therapeutics|September 26, 2025
Building Equitable Partnerships Between Industry Sponsors and Indigenous Communities to Enhance Engagement in Clinical TrialsLancer Stephens, Nicole Redvers, Maile Taualii, et al.
Neurology|March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyriaA C Jansen, A Oostra, B Desprechins, et al.
European Journal of Neurology|October 25, 2007
Infantile presentation of the mitochondrial A8344G mutationE Scalais, C Nuttin, S Seneca, et al.
Human Mutation|January 1, 1996
Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.
Human Reproduction (Oxford, England)|April 15, 2008
Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosisW Verpoest, M De Rademaeker, K Sermon, et al.
Pageof 6

Showing results (41-50 of 60) with videos related to

Sort By:
Pageof 6
Journal of Clinical Pathology|February 3, 2009
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defectsB De Paepe, J Smet, M Lammens, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit XL De Meirleir, W Lissens, C Benelli, et al.
Genes & Diseases|October 6, 2025
Transcriptional profiling reveals glucose-dependent regulation of <i>COL13A1</i> mRNA in Pompe patients: Prospect for a novel disease mechanismS Uyttebroeck, D V Ngoc, R Osei, et al.
American Journal of Medical Genetics. Part A|June 10, 2003
Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex IIRudy Van Coster, S Seneca, J Smet, et al.
Molecular and Cellular Endocrinology|September 29, 2001
PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndromeK Sermon, S Seneca, M De Rycke, et al.
Clinical Therapeutics|September 26, 2025
Building Equitable Partnerships Between Industry Sponsors and Indigenous Communities to Enhance Engagement in Clinical TrialsLancer Stephens, Nicole Redvers, Maile Taualii, et al.
Neurology|March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyriaA C Jansen, A Oostra, B Desprechins, et al.
European Journal of Neurology|October 25, 2007
Infantile presentation of the mitochondrial A8344G mutationE Scalais, C Nuttin, S Seneca, et al.
Human Mutation|January 1, 1996
Mutation analysis of the pyruvate dehydrogenase E1 alpha gene in eight patients with a pyruvate dehydrogenase complex deficiencyW Lissens, L De Meirleir, S Seneca, et al.
Human Reproduction (Oxford, England)|April 15, 2008
Real and expected delivery rates of patients with myotonic dystrophy undergoing intracytoplasmic sperm injection and preimplantation genetic diagnosisW Verpoest, M De Rademaeker, K Sermon, et al.
Pageof 6