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Pharmacology & Therapeutics
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May 18, 2023
Targeting mitochondrial function in macrophages: A novel treatment strategy for atherosclerotic cardiovascular disease?
Pierre-Hadrien Becker, Patrice Thérond, Pauline Gaignard
BMJ Case Reports
|
June 14, 2018
Primary carnitine deficiency in a 57-year-old patient with recurrent exertional rhabdomyolysis
Andoni Echaniz-Laguna, Valérie Biancalana, Pauline Gaignard, et al.
Frontiers in Aging Neuroscience
|
December 23, 2017
Role of Sex Hormones on Brain Mitochondrial Function, with Special Reference to Aging and Neurodegenerative Diseases
Pauline Gaignard, Philippe Liere, Patrice Thérond, et al.
Molecular Genetics and Metabolism
|
August 3, 2014
Liver transcript analysis reveals aberrant splicing due to silent and intronic variations in the ABCB11 gene
Anne Davit-Spraul, Christophe Oliveira, Emmanuel Gonzales, et al.
Journal of Human Genetics
|
March 10, 2017
UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia
Pauline Gaignard, Didier Eyer, Elise Lebigot, et al.
Cellular and Molecular Neurobiology
|
October 11, 2018
Steroids in Stroke with Special Reference to Progesterone
Rachida Guennoun, Xiaoyan Zhu, Magalie Fréchou, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 4, 2020
Brain White Matter Lesions and Presumed Crohn's Disease: Did You Consider MNGIE?
Louis Cousyn, Vanessa Boehm, Natalia Shor, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
December 15, 2015
Progesterone reduces brain mitochondrial dysfunction after transient focal ischemia in male and female mice
Pauline Gaignard, Magalie Fréchou, Michael Schumacher, et al.
Gene
|
October 11, 2012
Characterization of seven novel mutations on the HEXB gene in French Sandhoff patients
Pauline Gaignard, Jérôme Fagart, Natalia Niemir, et al.
European Journal of Medical Genetics
|
November 29, 2023
New description of an MRPS2 homozygous patient: Further features to help expend the phenotype
Thalia Papadopoulos, Pauline Gaignard, Manuel Schiff, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 49) with videos related to
Sort By:
Page
of 5
Pharmacology & Therapeutics
|
May 18, 2023
Targeting mitochondrial function in macrophages: A novel treatment strategy for atherosclerotic cardiovascular disease?
Pierre-Hadrien Becker, Patrice Thérond, Pauline Gaignard
BMJ Case Reports
|
June 14, 2018
Primary carnitine deficiency in a 57-year-old patient with recurrent exertional rhabdomyolysis
Andoni Echaniz-Laguna, Valérie Biancalana, Pauline Gaignard, et al.
Frontiers in Aging Neuroscience
|
December 23, 2017
Role of Sex Hormones on Brain Mitochondrial Function, with Special Reference to Aging and Neurodegenerative Diseases
Pauline Gaignard, Philippe Liere, Patrice Thérond, et al.
Molecular Genetics and Metabolism
|
August 3, 2014
Liver transcript analysis reveals aberrant splicing due to silent and intronic variations in the ABCB11 gene
Anne Davit-Spraul, Christophe Oliveira, Emmanuel Gonzales, et al.
Journal of Human Genetics
|
March 10, 2017
UQCRC2 mutation in a patient with mitochondrial complex III deficiency causing recurrent liver failure, lactic acidosis and hypoglycemia
Pauline Gaignard, Didier Eyer, Elise Lebigot, et al.
Cellular and Molecular Neurobiology
|
October 11, 2018
Steroids in Stroke with Special Reference to Progesterone
Rachida Guennoun, Xiaoyan Zhu, Magalie Fréchou, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 4, 2020
Brain White Matter Lesions and Presumed Crohn's Disease: Did You Consider MNGIE?
Louis Cousyn, Vanessa Boehm, Natalia Shor, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism
|
December 15, 2015
Progesterone reduces brain mitochondrial dysfunction after transient focal ischemia in male and female mice
Pauline Gaignard, Magalie Fréchou, Michael Schumacher, et al.
Gene
|
October 11, 2012
Characterization of seven novel mutations on the HEXB gene in French Sandhoff patients
Pauline Gaignard, Jérôme Fagart, Natalia Niemir, et al.
European Journal of Medical Genetics
|
November 29, 2023
New description of an MRPS2 homozygous patient: Further features to help expend the phenotype
Thalia Papadopoulos, Pauline Gaignard, Manuel Schiff, et al.
Page
of 5