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Hand Surgery & Rehabilitation
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July 25, 2023
Radiolunate arthrodesis and scaphoidectomy combined to Sauvé-Kapandji procedure as treatment of wrist osteoarthritis: Clinical and radiological results
Rémy Pichard, Marc Juvenspan, Patrick Houvet, et al.
The Journal of Pediatrics
|
October 13, 2009
Cardiomyopathies in propionic aciduria are reversible after liver transplantation
Stéphane Romano, Vassili Valayannopoulos, Guy Touati, et al.
European Journal of Pediatrics
|
October 4, 2007
What's new in metabolic and genetic hypoglycaemias: diagnosis and management
Vassili Valayannopoulos, Stéphane Romano, Karine Mention, et al.
Human Mutation
|
March 24, 2009
Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency
Sophie 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 encephalopathy
Magalie Barth, Chris Ottolenghi, Laurence Hubert, et al.
Human Mutation
|
September 25, 2009
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Hand Surgery & Rehabilitation
|
July 25, 2023
Radiolunate arthrodesis and scaphoidectomy combined to Sauvé-Kapandji procedure as treatment of wrist osteoarthritis: Clinical and radiological results
Rémy Pichard, Marc Juvenspan, Patrick Houvet, et al.
The Journal of Pediatrics
|
October 13, 2009
Cardiomyopathies in propionic aciduria are reversible after liver transplantation
Stéphane Romano, Vassili Valayannopoulos, Guy Touati, et al.
European Journal of Pediatrics
|
October 4, 2007
What's new in metabolic and genetic hypoglycaemias: diagnosis and management
Vassili Valayannopoulos, Stéphane Romano, Karine Mention, et al.
Human Mutation
|
March 24, 2009
Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency
Sophie 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 encephalopathy
Magalie Barth, Chris Ottolenghi, Laurence Hubert, et al.
Human Mutation
|
September 25, 2009
CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation
Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, et al.
Page
of 1