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Mathilde Doyard

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

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Indian Pediatrics|May 10, 2016
Ghosal Type Hematodiaphyseal DysplasiaAmrit Jeevan, Mathilde Doyard, Madhulika Kabra, et al.
Plos One|February 2, 2016
Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of HemochromatosissMathilde Doyard, Daniel Chappard, Patricia Leroyer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 18, 2020
Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis ImperfectaJohanne Dubail, Perrine Brunelle, Geneviève Baujat, et al.
Haematologica|March 18, 2024
Low-dose non-steroidal anti-inflammatory drugs: a promising approach for the treatment of symptomatic bone marrow failure in Ghosal hematodiaphyseal dysplasiaJonathan Bordat, Felipe Suarez, Valérie Cormier-Daire, et al.
Human Mutation|December 16, 2014
Mutations in SNRPB, encoding components of the core splicing machinery, cause cerebro-costo-mandibular syndromeSéverine Bacrot, Mathilde Doyard, Céline Huber, et al.
Journal of Medical Genetics|January 24, 2018
<i>FAM46A</i> mutations are responsible for autosomal recessive osteogenesis imperfectaMathilde Doyard, Séverine Bacrot, Céline Huber, et al.
Pageof 1

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

Sort By:
Pageof 1
Indian Pediatrics|May 10, 2016
Ghosal Type Hematodiaphyseal DysplasiaAmrit Jeevan, Mathilde Doyard, Madhulika Kabra, et al.
Plos One|February 2, 2016
Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of HemochromatosissMathilde Doyard, Daniel Chappard, Patricia Leroyer, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|March 18, 2020
Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis ImperfectaJohanne Dubail, Perrine Brunelle, Geneviève Baujat, et al.
Haematologica|March 18, 2024
Low-dose non-steroidal anti-inflammatory drugs: a promising approach for the treatment of symptomatic bone marrow failure in Ghosal hematodiaphyseal dysplasiaJonathan Bordat, Felipe Suarez, Valérie Cormier-Daire, et al.
Human Mutation|December 16, 2014
Mutations in SNRPB, encoding components of the core splicing machinery, cause cerebro-costo-mandibular syndromeSéverine Bacrot, Mathilde Doyard, Céline Huber, et al.
Journal of Medical Genetics|January 24, 2018
<i>FAM46A</i> mutations are responsible for autosomal recessive osteogenesis imperfectaMathilde Doyard, Séverine Bacrot, Céline Huber, et al.
Pageof 1