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Stéphane Romano

Showing results (1-10 of 6) with videos related to

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Hand Surgery & Rehabilitation|July 25, 2023
Radiolunate arthrodesis and scaphoidectomy combined to Sauvé-Kapandji procedure as treatment of wrist osteoarthritis: Clinical and radiological resultsRémy Pichard, Marc Juvenspan, Patrick Houvet, et al.
The Journal of Pediatrics|October 13, 2009
Cardiomyopathies in propionic aciduria are reversible after liver transplantationStéphane Romano, Vassili Valayannopoulos, Guy Touati, et al.
European Journal of Pediatrics|October 4, 2007
What's new in metabolic and genetic hypoglycaemias: diagnosis and managementVassili Valayannopoulos, Stéphane Romano, Karine Mention, et al.
Human Mutation|March 24, 2009
Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiencySophie Monnot, Valérie Serre, Bernadette Chadefaux-Vekemans, et al.
Journal of Inherited Metabolic Disease|October 28, 2010
Multiple sources of metabolic disturbance in ETHE1-related ethylmalonic encephalopathyMagalie Barth, Chris Ottolenghi, Laurence Hubert, et al.
Human Mutation|September 25, 2009
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlationSoumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Hand Surgery & Rehabilitation|July 25, 2023
Radiolunate arthrodesis and scaphoidectomy combined to Sauvé-Kapandji procedure as treatment of wrist osteoarthritis: Clinical and radiological resultsRémy Pichard, Marc Juvenspan, Patrick Houvet, et al.
The Journal of Pediatrics|October 13, 2009
Cardiomyopathies in propionic aciduria are reversible after liver transplantationStéphane Romano, Vassili Valayannopoulos, Guy Touati, et al.
European Journal of Pediatrics|October 4, 2007
What's new in metabolic and genetic hypoglycaemias: diagnosis and managementVassili Valayannopoulos, Stéphane Romano, Karine Mention, et al.
Human Mutation|March 24, 2009
Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiencySophie Monnot, Valérie Serre, Bernadette Chadefaux-Vekemans, et al.
Journal of Inherited Metabolic Disease|October 28, 2010
Multiple sources of metabolic disturbance in ETHE1-related ethylmalonic encephalopathyMagalie Barth, Chris Ottolenghi, Laurence Hubert, et al.
Human Mutation|September 25, 2009
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlationSoumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, et al.
Pageof 1