Espiard, Stéphanie
Inserm · Recherche translationnelle sur le diabète et les troubles métaboliques
7 papers on CoChatORCID 0000-0002-9584-4294
Most cited papers
- Verified
ARMC5 Mutations in Macronodular Adrenal Hyperplasia with Cushing's Syndrome
Assié, G., Libé, R., Espiard, S., Rizk-Rabin, M., Guimier, A., Luscap, W., Barreau, O., Lefèvre, L., Sibony, M., Guignat, L., et al. (2013) · New England Journal of Medicine
Adrenal and Paraganglionic TumorsAdrenal Hormones and Disorders
Cited by 395
- Verified
ARMC5 Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences
Espiard, S., Drougat, L., Libé, R., Assié, G., Perlemoine, K., Guignat, L., Barrande, G., Brucker-Davis, F., Doullay, F., Lopez, S., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism
Adrenal and Paraganglionic TumorsAdrenal Hormones and Disorders
Cited by 196
- Verified
Macronodular Adrenal Hyperplasia due to Mutations in an Armadillo Repeat Containing 5 (ARMC5) Gene: A Clinical and Genetic Investigation
Faucz, F. R., Zilbermint, M., Lodish, M. B., Szarek, E., Trivellin, G., Sinaii, N., Berthon, A., Libé, R., Assié, G., Espiard, S., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism
Adrenal and Paraganglionic TumorsAdrenal Hormones and Disorders
Cited by 166
- Verified
Ten-Year Outcome of Islet Alone or Islet After Kidney Transplantation in Type 1 Diabetes: A Prospective Parallel-Arm Cohort Study
Vantyghem, M.-C., Chetboun, M., Gmyr, V., Jannin, A., Espiard, S., Le Mapihan, K., Raverdy, V., Delalleau, N., Machuron, F., Hubert, T., et al. (2019) · Diabetes Care
Pancreatic function and diabetesDiabetes Management and Research
Cited by 105
- Verified
A Novel Mutation in THRA Gene Associated With an Atypical Phenotype of Resistance to Thyroid Hormone
Espiard, S., Savagner, F., Flamant, F., Vlaeminck-Guillem, V., Guyot, R., Munier, M., d'Herbomez, M., Bourguet, W., Pinto, G., Rose, C., et al. (2015) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsGenomics and Rare Diseases
Cited by 75
- Verified
Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome
Tabarin, A., Assié, G., Barat, P., Bonnet, F., Bonneville, J. F., Borson-Chazot, F., Bouligand, J., Boulin, A., Brue, T., Caron, P., et al. (2022) · Annales d Endocrinologie
Pituitary Gland Disorders and TreatmentsAdrenal Hormones and Disorders
Cited by 59
- Verified
TRα receptor mutations extend the spectrum of syndromes of reduced sensitivity to thyroid hormone
Vlaeminck-Guillem, V., Espiard, S., Flamant, F., & Wémeau, J.-L. (2015) · La Presse Médicale
Thyroid Disorders and TreatmentsGenomics and Rare Diseases
Cited by 17
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