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Yves Robitaille

Showing results (21-30 of 28) with videos related to

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Pediatric Research|June 17, 2008
Prenatal head growth and white matter injury in hypoplastic left heart syndromeRobert B Hinton, Gregor Andelfinger, Priya Sekar, et al.
Canadian Journal of Diabetes|April 14, 2023
Cardiovascular Risk Factors and Adherence to Cardiovascular Protection Practice Guidelines in Adults With Type 1 Diabetes: A BETTER Registry Cross-sectional AnalysisHoussein Madar, Marie-Laure Lalanne-Mistrih, Maha Lebbar, et al.
The American Journal of Pathology|May 22, 2003
hTERT gene amplification and increased mRNA expression in central nervous system embryonal tumorsXing Fan, Yunyue Wang, John Kratz, et al.
Journal of Medical Genetics|January 27, 2011
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiencyFrançois-Guillaume Debray, Charles Morin, Annie Janvier, et al.
Plos One|July 18, 2013
A liver-specific defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia and a distinct hepatic Acyl-CoA patternNicolas Gauthier, Jiang Wei Wu, Shu Pei Wang, et al.
The Journal of Clinical Endocrinology and Metabolism|October 30, 2008
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 geneEmilie Maquet, Sabine Costagliola, Jasmine Parma, et al.
Medicine|January 19, 2017
Atorvastatin-induced necrotizing autoimmune myositis: An emerging dominant entity in patients with autoimmune myositis presenting with a pure polymyositis phenotypeYves Troyanov, Océane Landon-Cardinal, Marvin J Fritzler, et al.
American Journal of Human Genetics|January 26, 2010
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophiesVéronique Bolduc, Gareth Marlow, Kym M Boycott, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Pediatric Research|June 17, 2008
Prenatal head growth and white matter injury in hypoplastic left heart syndromeRobert B Hinton, Gregor Andelfinger, Priya Sekar, et al.
Canadian Journal of Diabetes|April 14, 2023
Cardiovascular Risk Factors and Adherence to Cardiovascular Protection Practice Guidelines in Adults With Type 1 Diabetes: A BETTER Registry Cross-sectional AnalysisHoussein Madar, Marie-Laure Lalanne-Mistrih, Maha Lebbar, et al.
The American Journal of Pathology|May 22, 2003
hTERT gene amplification and increased mRNA expression in central nervous system embryonal tumorsXing Fan, Yunyue Wang, John Kratz, et al.
Journal of Medical Genetics|January 27, 2011
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiencyFrançois-Guillaume Debray, Charles Morin, Annie Janvier, et al.
Plos One|July 18, 2013
A liver-specific defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia and a distinct hepatic Acyl-CoA patternNicolas Gauthier, Jiang Wei Wu, Shu Pei Wang, et al.
The Journal of Clinical Endocrinology and Metabolism|October 30, 2008
Lethal respiratory failure and mild primary hypothyroidism in a term girl with a de novo heterozygous mutation in the TITF1/NKX2.1 geneEmilie Maquet, Sabine Costagliola, Jasmine Parma, et al.
Medicine|January 19, 2017
Atorvastatin-induced necrotizing autoimmune myositis: An emerging dominant entity in patients with autoimmune myositis presenting with a pure polymyositis phenotypeYves Troyanov, Océane Landon-Cardinal, Marvin J Fritzler, et al.
American Journal of Human Genetics|January 26, 2010
Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophiesVéronique Bolduc, Gareth Marlow, Kym M Boycott, et al.
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