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Thomas Edouard

Showing results (71-80 of 80) with videos related to

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Hormone Research in Paediatrics|December 1, 2025
EndoCompass Project: Research Roadmap for Growth DisordersEvelien F Gevers, Anita C Hokken-Koelega, Maithe Tauber, et al.
European Heart Journal|May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trialOlivier Milleron, Florence Arnoult, Jacques Ropers, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 29, 2006
[Recommendations for the medical management of aortic complications of Marfan's syndrome]Guillaume Jondeau, Martine Barthelet, Clarisse Baumann, et al.
Calcified Tissue International|September 24, 2024
Early-Onset Osteoporosis: Molecular Analysis in Large Cohort and Focus on the PLS3 GeneMaxence Mancini, Roland Chapurlat, Bertrand Isidor, et al.
European Journal of Endocrinology|December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric populationYasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
Science Translational Medicine|April 29, 2021
SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populationsRomain Paccoud, Céline Saint-Laurent, Enzo Piccolo, et al.
European Journal of Endocrinology|January 16, 2026
International guideline on genetic testing of children with short statureAndrew Dauber, Alexander A L Jorge, Ola Nilsson, et al.
European Journal of Human Genetics : EJHG|February 20, 2009
A large-scale mutation search reveals genetic heterogeneity in 3M syndromeCéline Huber, Anee-Lise Delezoide, Fabien Guimiot, et al.
The New England Journal of Medicine|June 29, 2026
Phase 3 Trial of Oral Infigratinib in Children with AchondroplasiaRavi Savarirayan, Julie Hoover-Fong, Melita Irving, et al.
American Journal of Human Genetics|May 19, 2021
Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulationAlban Ziegler, Rémi Duclaux-Loras, Céline Revenu, et al.
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Showing results (71-80 of 80) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 80 results.
Hormone Research in Paediatrics|December 1, 2025
EndoCompass Project: Research Roadmap for Growth DisordersEvelien F Gevers, Anita C Hokken-Koelega, Maithe Tauber, et al.
European Heart Journal|May 4, 2015
Marfan Sartan: a randomized, double-blind, placebo-controlled trialOlivier Milleron, Florence Arnoult, Jacques Ropers, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 29, 2006
[Recommendations for the medical management of aortic complications of Marfan's syndrome]Guillaume Jondeau, Martine Barthelet, Clarisse Baumann, et al.
Calcified Tissue International|September 24, 2024
Early-Onset Osteoporosis: Molecular Analysis in Large Cohort and Focus on the PLS3 GeneMaxence Mancini, Roland Chapurlat, Bertrand Isidor, et al.
European Journal of Endocrinology|December 28, 2020
Presenting features and molecular genetics of primary hyperparathyroidism in the paediatric populationYasmine El Allali, Coralie Hermetet, Justine Bacchetta, et al.
Science Translational Medicine|April 29, 2021
SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populationsRomain Paccoud, Céline Saint-Laurent, Enzo Piccolo, et al.
European Journal of Endocrinology|January 16, 2026
International guideline on genetic testing of children with short statureAndrew Dauber, Alexander A L Jorge, Ola Nilsson, et al.
European Journal of Human Genetics : EJHG|February 20, 2009
A large-scale mutation search reveals genetic heterogeneity in 3M syndromeCéline Huber, Anee-Lise Delezoide, Fabien Guimiot, et al.
The New England Journal of Medicine|June 29, 2026
Phase 3 Trial of Oral Infigratinib in Children with AchondroplasiaRavi Savarirayan, Julie Hoover-Fong, Melita Irving, et al.
American Journal of Human Genetics|May 19, 2021
Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulationAlban Ziegler, Rémi Duclaux-Loras, Céline Revenu, et al.
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