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European Journal of Pediatrics
|
September 21, 2011
Efficacy and safety of 2-year etidronate treatment in a child with generalized arterial calcification of infancy
Thomas Edouard, Gilles Chabot, Joaquim Miro, et al.
The American Journal of Cardiology
|
January 31, 2007
Effect of beta-blockade on ascending aortic dilatation in children with the Marfan syndrome
Magalie Ladouceur, Christophe Fermanian, Jean-Marc Lupoglazoff, et al.
Molecular and Cellular Endocrinology
|
October 1, 2011
Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19
Héctor M Targovnik, Thomas Edouard, Viviana Varela, et al.
European Journal of Endocrinology
|
March 3, 2026
Once-weekly Somapacitan in Children with Noonan Syndrome: Randomised Controlled Phase 3 Trial
Alexander A L Jorge, Assunta Albanese, Michael Højby, et al.
Endocrine Connections
|
March 4, 2022
Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status
Alexander A L Jorge, Thomas Edouard, Mohamad Maghnie, et al.
European Journal of Human Genetics : EJHG
|
September 23, 2025
Expanding the molecular spectrum of aggrecanopathies: exploring 24 patients with ACAN significant variants
Melek Trigui, Nathalie Pallares-Ruiz, David Geneviève, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 19, 2011
Low bone mass and high material bone density in two patients with Loeys-Dietz syndrome caused by transforming growth factor beta receptor 2 mutations
I Mouna Ben Amor, Thomas Edouard, Francis H Glorieux, et al.
Molecular and Cellular Biology
|
November 21, 2007
Signal strength dictates phosphoinositide 3-kinase contribution to Ras/extracellular signal-regulated kinase 1 and 2 activation via differential Gab1/Shp2 recruitment: consequences for resistance to epidermal growth factor receptor inhibition
Carla Sampaio, Marie Dance, Alexandra Montagner, et al.
Hormone Research in Paediatrics
|
January 26, 2025
Real-World Safety and Effectiveness of Vosoritide in Children with Achondroplasia: French Early Access Program
Valérie Cormier-Daire, Thomas Edouard, Bertrand Isidor, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 14, 2007
Identification of a novel mutation in the human growth hormone receptor gene (GHR) in a patient with Laron syndrome
Isabelle Gennero, Thomas Edouard, Mona Rashad, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 80) with videos related to
Sort By:
Page
of 8
European Journal of Pediatrics
|
September 21, 2011
Efficacy and safety of 2-year etidronate treatment in a child with generalized arterial calcification of infancy
Thomas Edouard, Gilles Chabot, Joaquim Miro, et al.
The American Journal of Cardiology
|
January 31, 2007
Effect of beta-blockade on ascending aortic dilatation in children with the Marfan syndrome
Magalie Ladouceur, Christophe Fermanian, Jean-Marc Lupoglazoff, et al.
Molecular and Cellular Endocrinology
|
October 1, 2011
Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19
Héctor M Targovnik, Thomas Edouard, Viviana Varela, et al.
European Journal of Endocrinology
|
March 3, 2026
Once-weekly Somapacitan in Children with Noonan Syndrome: Randomised Controlled Phase 3 Trial
Alexander A L Jorge, Assunta Albanese, Michael Højby, et al.
Endocrine Connections
|
March 4, 2022
Outcomes in growth hormone-treated Noonan syndrome children: impact of PTPN11 mutation status
Alexander A L Jorge, Thomas Edouard, Mohamad Maghnie, et al.
European Journal of Human Genetics : EJHG
|
September 23, 2025
Expanding the molecular spectrum of aggrecanopathies: exploring 24 patients with ACAN significant variants
Melek Trigui, Nathalie Pallares-Ruiz, David Geneviève, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 19, 2011
Low bone mass and high material bone density in two patients with Loeys-Dietz syndrome caused by transforming growth factor beta receptor 2 mutations
I Mouna Ben Amor, Thomas Edouard, Francis H Glorieux, et al.
Molecular and Cellular Biology
|
November 21, 2007
Signal strength dictates phosphoinositide 3-kinase contribution to Ras/extracellular signal-regulated kinase 1 and 2 activation via differential Gab1/Shp2 recruitment: consequences for resistance to epidermal growth factor receptor inhibition
Carla Sampaio, Marie Dance, Alexandra Montagner, et al.
Hormone Research in Paediatrics
|
January 26, 2025
Real-World Safety and Effectiveness of Vosoritide in Children with Achondroplasia: French Early Access Program
Valérie Cormier-Daire, Thomas Edouard, Bertrand Isidor, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
September 14, 2007
Identification of a novel mutation in the human growth hormone receptor gene (GHR) in a patient with Laron syndrome
Isabelle Gennero, Thomas Edouard, Mona Rashad, et al.
Page
of 8