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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 defects
B De Paepe, J Smet, M Lammens, et al.
Journal of Inherited Metabolic Disease
|
March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit X
L 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 mechanism
S 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 II
Rudy 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 syndrome
K 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 Trials
Lancer Stephens, Nicole Redvers, Maile Taualii, et al.
Neurology
|
March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria
A C Jansen, A Oostra, B Desprechins, et al.
European Journal of Neurology
|
October 25, 2007
Infantile presentation of the mitochondrial A8344G mutation
E 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 deficiency
W 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 diagnosis
W Verpoest, M De Rademaeker, K Sermon, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 60) with videos related to
Sort By:
Page
of 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 defects
B De Paepe, J Smet, M Lammens, et al.
Journal of Inherited Metabolic Disease
|
March 21, 1998
Pyruvate dehydrogenase complex deficiency and absence of subunit X
L 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 mechanism
S 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 II
Rudy 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 syndrome
K 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 Trials
Lancer Stephens, Nicole Redvers, Maile Taualii, et al.
Neurology
|
March 16, 2011
TUBA1A mutations: from isolated lissencephaly to familial polymicrogyria
A C Jansen, A Oostra, B Desprechins, et al.
European Journal of Neurology
|
October 25, 2007
Infantile presentation of the mitochondrial A8344G mutation
E 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 deficiency
W 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 diagnosis
W Verpoest, M De Rademaeker, K Sermon, et al.
Page
of 6