Kolexia
Tardy Veronique
Biologie médicale
Hôpital Femme Mère Enfant
Bron, France
40 Activités
98 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
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Industries

Merck-Serono
2 collaboration(s)
Dernière en 2019
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Dernières activités

The experience of diagnosis announcement in rare endocrine diseases: A survey of the French FIRENDO network.
Annales d'endocrinologie   10 novembre 2023
Fertility and pregnancy outcomes in women with nonclassic 21-hydroxylase deficiency.
Clinical endocrinology   17 novembre 2022
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
Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe.
European journal of endocrinology   23 mars 2022
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
Optimized nested PCR enhances biological diagnosis and phylogenetic analysis of human parvovirus B19 infections.
Archives of virology   10 août 2019
Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in Gene.
Frontiers in endocrinology   05 septembre 2018
News about the genetics of congenital primary adrenal insufficiency.
Annales d'endocrinologie   13 avril 2018
Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India.
The Indian journal of medical research   21 mars 2018