Véronique Tardy - Concepedia

Author

Véronique Tardy

Also Known As

Anamaria Stetco, L. Duranteau, Sophie Dahoun, V Tardy, V. Tardy, V??ronique Tardy, Veronique Tardy, Véronique Tardy, Véronique Tardy

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Inserm Assistance Publique – Hôpitaux de Paris Université Paris Cité Université Claude Bernard Lyon 1 Hôpital Debrousse

About

Véronique Tardy is an author at Inserm specializing in medicine, adrenal disease, and adrenal health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	274
2	Endocrinology	3	3	186
3	Obstetrics	2	2	174
4	Pathology	2	2	100
5	Clinical Genetics	2	2	231

Véronique Tardy

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Clinical and Molecular Characterization of a Cohort of 161 Unrelated Women with Nonclassical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency and 330 Family Members Maud Bidet, Christine Bellanné‐Chantelot, Marie-Béatrice Galand-Portier, The Journal of Clinical Endocrinology & Metabolism	2009	208
Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Maud Bidet, Christine Bellanné‐Chantelot, Marie-Béatrice Galand-Portier, The Journal of Clinical Endocrinology & Metabolism	2010	199
Phenotype-Genotype Correlation in 56 Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency Catherine Deneux‐Tharaux, Véronique Tardy, Anne Dib, The Journal of Clinical Endocrinology & Metabolism GeneticsGenetic EpidemiologyGynecologyClinical GeneticsAdrenal Gland	2001	143
Precocious Pubarche: Distinguishing Late-Onset Congenital Adrenal Hyperplasia from Premature Adrenarche Jean-Baptiste Armengaud, Marie‐Laure Charkaluk, Christine Trivin, The Journal of Clinical Endocrinology & Metabolism	2009	133
New Insight into the Molecular Basis of 3β-Hydroxysteroid Dehydrogenase Deficiency: Identification of Eight Mutations in the HSD3B2 Gene in Eleven Patients from Seven New Families and Comparison of the Functional Properties of Twenty-Five Mutant Enzymes1 Anne Marie Moisan, Marie‐Louise Ricketts, Véronique Tardy, The Journal of Clinical Endocrinology & Metabolism	1999	105
Follow-Up of 68 Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Relevance of Genotype for Management Graziella Pinto, Véronique Tardy, Christine Trivin, The Journal of Clinical Endocrinology & Metabolism	2003	102
Molecular Genetic Analysis of Tunisian Patients with a Classic Form of 21-Hydroxylase Deficiency: Identification of Four Novel Mutations and High Prevalence of Q318X Mutation Maher Kharrat, Véronique Tardy, Ridha Mrad, The Journal of Clinical Endocrinology & Metabolism Mendelian DisorderCongenital Adrenal HyperplasiaCyp21 Active GeneMedicineGenetics	2004	88
How a Patient Homozygous for a 30-kb Deletion of the C4-CYP 21 Genomic Region Can Have a Nonclassic Form of 21-Hydroxylase Deficiency Dagmar l’Allemand, Véronique Tardy, Annette Grüters, The Journal of Clinical Endocrinology & Metabolism	2000	76
Phenotype-Genotype Correlations of 13 Rare CYP21A2 Mutations Detected in 46 Patients Affected with 21-Hydroxylase Deficiency and in One Carrier Véronique Tardy, Rita Menassa, V. Sulmont, The Journal of Clinical Endocrinology & Metabolism	2010	71
Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia Paolo Cavarzere, Dinane Samara‐Boustani, Isabelle Flechtner, European Journal of Endocrinology	2009	38

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