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François M Petit

Showing results (1-10 of 21) with videos related to

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Biochemical Society Transactions|November 18, 2014
Moonlighting proteins in sperm-egg interactionsFrançois M Petit, Catherine Serres, Jana Auer
Current Opinion in Oncology|March 26, 2023
Targeting Harvey rat sarcoma viral oncogene homolog in head and neck cancer: how to move forward?Hédi Ben Yahia, François M Petit, Esma Saada-Bouzid
Neuromuscular Disorders : NMD|October 1, 2013
PNPLA2 mutation: a paediatric case with early onset but indolent courseLaurine Perrin, Léonard Féasson, Alain Furby, et al.
Journal of Inherited Metabolic Disease|November 25, 2010
Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type IbAlix Mollet Boudjemline, Arnaud Isapof, Jean-Bernard Witas, et al.
Journal of the Neurological Sciences|February 28, 2012
Juvenile-onset permanent weakness in muscle phosphofructokinase deficiencyEdoardo Malfatti, Nazha Birouk, Norma B Romero, et al.
Journal of Andrology|February 17, 2005
Could sperm aneuploidy rate determination be used as a predictive test before intracytoplasmic sperm injection?François M Petit, Nelly Frydman, Moncef Benkhalifa, et al.
European Journal of Human Genetics : EJHG|December 9, 2004
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndromeFrançois M Petit, Vincent Gajdos, Frédéric Parisot, et al.
Molecular Genetics and Metabolism|January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic studyPascal Laforêt, Tanya Stojkovic, Guillaume Bassez, et al.
Journal of the Neurological Sciences|April 2, 2021
A novel PHKA1 mutation associating myopathy and cognitive impairment: Expanding the spectrum of phosphorylase kinase b (PhK) deficiencyMichela Bisciglia, Roseline Froissart, Anne Laure Bedat-Millet, et al.
Molecular Cytogenetics|February 12, 2015
Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent diseaseNarjes Armanet, Corinne Metay, Sophie Brisset, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Biochemical Society Transactions|November 18, 2014
Moonlighting proteins in sperm-egg interactionsFrançois M Petit, Catherine Serres, Jana Auer
Current Opinion in Oncology|March 26, 2023
Targeting Harvey rat sarcoma viral oncogene homolog in head and neck cancer: how to move forward?Hédi Ben Yahia, François M Petit, Esma Saada-Bouzid
Neuromuscular Disorders : NMD|October 1, 2013
PNPLA2 mutation: a paediatric case with early onset but indolent courseLaurine Perrin, Léonard Féasson, Alain Furby, et al.
Journal of Inherited Metabolic Disease|November 25, 2010
Klüver Bucy syndrome following hypoglycaemic coma in a patient with glycogen storage disease type IbAlix Mollet Boudjemline, Arnaud Isapof, Jean-Bernard Witas, et al.
Journal of the Neurological Sciences|February 28, 2012
Juvenile-onset permanent weakness in muscle phosphofructokinase deficiencyEdoardo Malfatti, Nazha Birouk, Norma B Romero, et al.
Journal of Andrology|February 17, 2005
Could sperm aneuploidy rate determination be used as a predictive test before intracytoplasmic sperm injection?François M Petit, Nelly Frydman, Moncef Benkhalifa, et al.
European Journal of Human Genetics : EJHG|December 9, 2004
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndromeFrançois M Petit, Vincent Gajdos, Frédéric Parisot, et al.
Molecular Genetics and Metabolism|January 22, 2013
Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic studyPascal Laforêt, Tanya Stojkovic, Guillaume Bassez, et al.
Journal of the Neurological Sciences|April 2, 2021
A novel PHKA1 mutation associating myopathy and cognitive impairment: Expanding the spectrum of phosphorylase kinase b (PhK) deficiencyMichela Bisciglia, Roseline Froissart, Anne Laure Bedat-Millet, et al.
Molecular Cytogenetics|February 12, 2015
Double Xp11.22 deletion including SHROOM4 and CLCN5 associated with severe psychomotor retardation and Dent diseaseNarjes Armanet, Corinne Metay, Sophie Brisset, et al.
Pageof 3