Kolexia
Morel Yves
Médecine générale
Hôpital Femme Mère Enfant
Bron, France
66 Activités
0 Followers

Scientifique
Digital
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Expertise
Sujets de recherche
{{person.topmesh1.name}} Hyperplasie congénitale des surrénales Troubles du développement sexuel Hyperplasie Insuffisance surrénale Dysgénésie gonadique 46, XY Virilisme Troubles du développement sexuel de sujets 46, XX Hypoaldostéronisme Hypospadias

Industries

Merck-Serono
1 collaboration(s)
Dernière en 2018
Sandoz
1 collaboration(s)
Dernière en 2018
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Dernières activités

Loss of LGR4/GPR48 causes severe neonatal salt wasting due to disrupted WNT signaling altering adrenal zonation.
The Journal of clinical investigation   15 février 2023
Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria.
Frontiers in endocrinology   10 juin 2022
Clinical, biochemical, and biomolecular aspects of congenital adrenal hyperplasia in a group of Cameroonian children and adolescents.
Journal of pediatric endocrinology & metabolism : JPEM   02 mai 2022
Preoperative Topical Estrogen Treatment vs Placebo in 244 Children With Midshaft and Posterior Hypospadias.
The Journal of clinical endocrinology and metabolism   03 février 2021
Observational study of disorders of sex development in Yaounde, Cameroon.
Journal of pediatric endocrinology & metabolism : JPEM   07 décembre 2020
Exposure to Glucocorticoids in the First Part of Fetal Life is Associated with Insulin Secretory Defect in Adult Humans.
The Journal of clinical endocrinology and metabolism   06 novembre 2020
Hypopituitarism in Patients with Blepharophimosis and FOXL2 Mutations.
Hormone research in paediatrics   26 mai 2020
Letter to the Editor: "Characterization of the CYP11A1 Nonsynonymous Variant p.E314K in Children Presenting With Adrenal Insufficiency".
The Journal of clinical endocrinology and metabolism   17 février 2020
Disorder of sex development with germ cell tumors: Which is uncovered first?
Pediatric blood & cancer   04 février 2020
In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.
Reproductive biomedicine online   10 octobre 2019