Publications by authors named "Mathilde Doyard"

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Low-dose non-steroidal anti-inflammatory drugs: a promising approach for the treatment of symptomatic bone marrow failure in Ghosal hematodiaphyseal dysplasia.
Jonathan Bordat, Felipe Suarez, Valérie Cormier-Daire, Regis Peffault De Latour, Jean Soulier, Mathilde Doyard

Haematologica· August 2024

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Homozygous Loss-of-Function Mutations in CCDC134 Are Responsible for a Severe Form of Osteogenesis Imperfecta.
Johanne Dubail, Perrine Brunelle, Geneviève Baujat, Céline Huber, Mathilde Doyard

J Bone Miner Res· August 2020

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mutations are responsible for autosomal recessive osteogenesis imperfecta.
Mathilde Doyard, Séverine Bacrot, Céline Huber, Maja Di Rocco, Alice Goldenberg

J Med Genet· April 2018

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Decreased Bone Formation Explains Osteoporosis in a Genetic Mouse Model of Hemochromatosiss.
Mathilde Doyard, Daniel Chappard, Patricia Leroyer, Marie-Paule Roth, Olivier Loréal

PLoS One· July 2016

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Ghosal Type Hematodiaphyseal Dysplasia.
Amrit Jeevan, Mathilde Doyard, Madhulika Kabra, Valerie Cormier Daire, Neerja Gupta

Indian Pediatr· April 2016

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Mutations in SNRPB, encoding components of the core splicing machinery, cause cerebro-costo-mandibular syndrome.
Séverine Bacrot, Mathilde Doyard, Céline Huber, Olivier Alibeu, Niklas Feldhahn

Hum Mutat· February 2015

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