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Isabelle Guilhem

Showing results (11-20 of 15) with videos related to

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European Journal of Endocrinology|December 25, 2014
Long-term results of the surgical management of insulinoma patients with MEN1: a Groupe d'étude des Tumeurs Endocrines (GTE) retrospective studyDelphine Vezzosi, Catherine Cardot-Bauters, Nicolas Bouscaren, et al.
Diabetologia|May 23, 2024
Heterogeneity of glycaemic phenotypes in type 1 diabetesGuy Fagherazzi, Gloria A Aguayo, Lu Zhang, et al.
Human Molecular Genetics|February 5, 2013
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort studyJulien Thevenon, Abderrahmane Bourredjem, Laurence Faivre, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 29, 2012
MAX mutations cause hereditary and sporadic pheochromocytoma and paragangliomaNelly Burnichon, Alberto Cascón, Francesca Schiavi, et al.
BMC Public Health|September 30, 2016
Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control studyF Balazard, S Le Fur, S Valtat, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
European Journal of Endocrinology|December 25, 2014
Long-term results of the surgical management of insulinoma patients with MEN1: a Groupe d'étude des Tumeurs Endocrines (GTE) retrospective studyDelphine Vezzosi, Catherine Cardot-Bauters, Nicolas Bouscaren, et al.
Diabetologia|May 23, 2024
Heterogeneity of glycaemic phenotypes in type 1 diabetesGuy Fagherazzi, Gloria A Aguayo, Lu Zhang, et al.
Human Molecular Genetics|February 5, 2013
Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort studyJulien Thevenon, Abderrahmane Bourredjem, Laurence Faivre, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|March 29, 2012
MAX mutations cause hereditary and sporadic pheochromocytoma and paragangliomaNelly Burnichon, Alberto Cascón, Francesca Schiavi, et al.
BMC Public Health|September 30, 2016
Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control studyF Balazard, S Le Fur, S Valtat, et al.
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