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Catherine Brunel-Guitton

Showing results (1-10 of 32) with videos related to

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The Canadian Journal of Cardiology|November 1, 2015
Mitochondrial Diseases and CardiomyopathiesCatherine Brunel-Guitton, Alina Levtova, Florin Sasarman
Journal of Inherited Metabolic Disease|September 11, 2010
Treatment of cobalamin C (cblC) deficiency during pregnancyCatherine Brunel-Guitton, Teresa Costa, Grant A Mitchell, et al.
Molecular Biology of the Cell|March 5, 2010
LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondriaFlorin Sasarman, Catherine Brunel-Guitton, Hana Antonicka, et al.
American Journal of Medical Genetics. Part A|August 11, 2020
Prenatal pleural effusions and chylothorax: An unusual presentation for CM-AVM syndrome due to RASA1Guylaine D'Amours, Catherine Brunel-Guitton, Marie-Ange Delrue, et al.
Journal of Inherited Metabolic Disease|December 23, 2015
Biosynthesis of glycosaminoglycans: associated disorders and biochemical testsFlorin Sasarman, Catalina Maftei, Philippe M Campeau, et al.
The Journal of Pediatrics|May 29, 2017
ReplyChiraz Ghaddhab, Charles Morin, Catherine Brunel-Guitton, et al.
The Journal of Pediatrics|March 13, 2017
Premature Ovarian Failure in French Canadian Leigh SyndromeChiraz Ghaddhab, Charles Morin, Catherine Brunel-Guitton, et al.
Hepatic Medicine : Evidence and Research|September 27, 2018
Acute pediatric hyperammonemia: current diagnosis and management strategiesNadia Savy, David Brossier, Catherine Brunel-Guitton, et al.
Journal of Inherited Metabolic Disease|October 11, 2014
Inborn errors of cytoplasmic triglyceride metabolismJiang Wei Wu, Hao Yang, Shu Pei Wang, et al.
Molecular Genetics and Metabolism|March 18, 2011
Late-onset nonketotic hyperglycinemia caused by a novel homozygous missense mutation in the GLDC geneCatherine Brunel-Guitton, Brett Casey, Marion Coulter-Mackie, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
The Canadian Journal of Cardiology|November 1, 2015
Mitochondrial Diseases and CardiomyopathiesCatherine Brunel-Guitton, Alina Levtova, Florin Sasarman
Journal of Inherited Metabolic Disease|September 11, 2010
Treatment of cobalamin C (cblC) deficiency during pregnancyCatherine Brunel-Guitton, Teresa Costa, Grant A Mitchell, et al.
Molecular Biology of the Cell|March 5, 2010
LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondriaFlorin Sasarman, Catherine Brunel-Guitton, Hana Antonicka, et al.
American Journal of Medical Genetics. Part A|August 11, 2020
Prenatal pleural effusions and chylothorax: An unusual presentation for CM-AVM syndrome due to RASA1Guylaine D'Amours, Catherine Brunel-Guitton, Marie-Ange Delrue, et al.
Journal of Inherited Metabolic Disease|December 23, 2015
Biosynthesis of glycosaminoglycans: associated disorders and biochemical testsFlorin Sasarman, Catalina Maftei, Philippe M Campeau, et al.
The Journal of Pediatrics|May 29, 2017
ReplyChiraz Ghaddhab, Charles Morin, Catherine Brunel-Guitton, et al.
The Journal of Pediatrics|March 13, 2017
Premature Ovarian Failure in French Canadian Leigh SyndromeChiraz Ghaddhab, Charles Morin, Catherine Brunel-Guitton, et al.
Hepatic Medicine : Evidence and Research|September 27, 2018
Acute pediatric hyperammonemia: current diagnosis and management strategiesNadia Savy, David Brossier, Catherine Brunel-Guitton, et al.
Journal of Inherited Metabolic Disease|October 11, 2014
Inborn errors of cytoplasmic triglyceride metabolismJiang Wei Wu, Hao Yang, Shu Pei Wang, et al.
Molecular Genetics and Metabolism|March 18, 2011
Late-onset nonketotic hyperglycinemia caused by a novel homozygous missense mutation in the GLDC geneCatherine Brunel-Guitton, Brett Casey, Marion Coulter-Mackie, et al.
Pageof 4