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Thomas Edouard

Showing results (11-20 of 80) with videos related to

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Endocrine Reviews|June 21, 2018
The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK PathwayMylène Tajan, Romain Paccoud, Sophie Branka, et al.
Frontiers in Endocrinology|January 23, 2023
Editorial: Endocrine aspects of Noonan syndrome and related syndromesGiorgio Radetti, Thomas Edouard, Laura Mazzanti, et al.
European Journal of Medical Genetics|September 6, 2015
SHP2 sails from physiology to pathologyMylène Tajan, Audrey de Rocca Serra, Philippe Valet, et al.
Clinical Case Reports|December 12, 2017
Severe thyrotoxicosis in an infant revealing familial nonautoimmune hyperthyroidism with a novel (C672W) stimulating thyrotropin receptor germline mutationIsabelle Oliver-Petit, Frédérique Savagner, Solange Grunenwald, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 20, 2024
Survey on vitamin D supplementation in children in France: Evaluation of real-life practices following the new 2022 French recommendationsMarie Lou Pechabrier, Justine Bacchetta, Patrick Tounian, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2019
Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girlClaire Flot, Isabelle Oliver, Philippe Caron, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Muscle-bone characteristics in children with Prader-Willi syndromeThomas Edouard, Cheri Deal, Guy Van Vliet, et al.
Frontiers in Endocrinology|July 12, 2021
Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With DyshormonogenesisIsabelle Oliver-Petit, Thomas Edouard, Virginie Jacques, et al.
Children (Basel, Switzerland)|August 29, 2024
Orofacial Features, Oral Health-Related Quality of Life, and Exposure to Bullying in Osteogenesis Imperfecta: A Cross-Sectional StudyAlice Broutin, Jean-Pierre Salles, Valérie Porquet-Bordes, et al.
Annales D'Endocrinologie|January 16, 2025
Chapter 7: The different forms of primary hyperparathyroidism at different ages of life: Childhood, pregnancy, lactation, old ageMadleen Lemaitre, Clotilde Picart, Iva Gueorguieva, et al.
Pageof 8

Showing results (11-20 of 80) with videos related to

Sort By:
Pageof 8
Endocrine Reviews|June 21, 2018
The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK PathwayMylène Tajan, Romain Paccoud, Sophie Branka, et al.
Frontiers in Endocrinology|January 23, 2023
Editorial: Endocrine aspects of Noonan syndrome and related syndromesGiorgio Radetti, Thomas Edouard, Laura Mazzanti, et al.
European Journal of Medical Genetics|September 6, 2015
SHP2 sails from physiology to pathologyMylène Tajan, Audrey de Rocca Serra, Philippe Valet, et al.
Clinical Case Reports|December 12, 2017
Severe thyrotoxicosis in an infant revealing familial nonautoimmune hyperthyroidism with a novel (C672W) stimulating thyrotropin receptor germline mutationIsabelle Oliver-Petit, Frédérique Savagner, Solange Grunenwald, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 20, 2024
Survey on vitamin D supplementation in children in France: Evaluation of real-life practices following the new 2022 French recommendationsMarie Lou Pechabrier, Justine Bacchetta, Patrick Tounian, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2019
Acquired von Willebrand's syndrome caused by primary hypothyroidism in a 5-year-old girlClaire Flot, Isabelle Oliver, Philippe Caron, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Muscle-bone characteristics in children with Prader-Willi syndromeThomas Edouard, Cheri Deal, Guy Van Vliet, et al.
Frontiers in Endocrinology|July 12, 2021
Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With DyshormonogenesisIsabelle Oliver-Petit, Thomas Edouard, Virginie Jacques, et al.
Children (Basel, Switzerland)|August 29, 2024
Orofacial Features, Oral Health-Related Quality of Life, and Exposure to Bullying in Osteogenesis Imperfecta: A Cross-Sectional StudyAlice Broutin, Jean-Pierre Salles, Valérie Porquet-Bordes, et al.
Annales D'Endocrinologie|January 16, 2025
Chapter 7: The different forms of primary hyperparathyroidism at different ages of life: Childhood, pregnancy, lactation, old ageMadleen Lemaitre, Clotilde Picart, Iva Gueorguieva, et al.
Pageof 8