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Estradiol levels in men with congenital hypogonadotropic hypogonadism and the effects of different modalities of hormonal treatment.
Trabado S, Maione L, Salenave S, Baron S, Galland F, Bry-Gauillard H, Guiochon-Mantel A, Chanson P, Pitteloud N, Sinisi AA, Brailly-Tabard S, Young J. Trabado S, et al. Among authors: baron s. Fertil Steril. 2011 Jun;95(7):2324-9, 2329.e1-3. doi: 10.1016/j.fertnstert.2011.03.091. Epub 2011 May 4. Fertil Steril. 2011. PMID: 21536274 Free article.
SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome.
Hanchate NK, Giacobini P, Lhuillier P, Parkash J, Espy C, Fouveaut C, Leroy C, Baron S, Campagne C, Vanacker C, Collier F, Cruaud C, Meyer V, García-Piñero A, Dewailly D, Cortet-Rudelli C, Gersak K, Metz C, Chabrier G, Pugeat M, Young J, Hardelin JP, Prevot V, Dodé C. Hanchate NK, et al. Among authors: baron s. PLoS Genet. 2012 Aug;8(8):e1002896. doi: 10.1371/journal.pgen.1002896. Epub 2012 Aug 23. PLoS Genet. 2012. PMID: 22927827 Free PMC article.
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
Vargas-Poussou R, Mansour-Hendili L, Baron S, Bertocchio JP, Travers C, Simian C, Treard C, Baudouin V, Beltran S, Broux F, Camard O, Cloarec S, Cormier C, Debussche X, Dubosclard E, Eid C, Haymann JP, Kiando SR, Kuhn JM, Lefort G, Linglart A, Lucas-Pouliquen B, Macher MA, Maruani G, Ouzounian S, Polak M, Requeda E, Robier D, Silve C, Souberbielle JC, Tack I, Vezzosi D, Jeunemaitre X, Houillier P. Vargas-Poussou R, et al. Among authors: baron s. J Clin Endocrinol Metab. 2016 May;101(5):2185-95. doi: 10.1210/jc.2015-3442. Epub 2016 Mar 10. J Clin Endocrinol Metab. 2016. PMID: 26963950
Pro-FHH: A Risk Equation to Facilitate the Diagnosis of Parathyroid-Related Hypercalcemia.
Bertocchio JP, Tafflet M, Koumakis E, Maruani G, Vargas-Poussou R, Silve C, Nissen PH, Baron S, Prot-Bertoye C, Courbebaisse M, Souberbielle JC, Rejnmark L, Cormier C, Houillier P. Bertocchio JP, et al. Among authors: baron s. J Clin Endocrinol Metab. 2018 Jul 1;103(7):2534-2542. doi: 10.1210/jc.2017-02773. J Clin Endocrinol Metab. 2018. PMID: 29727008
Deciphering the Role of Vasopressin in Primary Aldosteronism.
Nogueira-Silva L, Blanchard A, Curis E, Lorthioir A, Zhygalina V, Bergerot D, Baron S, Amar L, Bobrie G, Plouin PF, Ménard J, Azizi M. Nogueira-Silva L, et al. Among authors: baron s. J Clin Endocrinol Metab. 2015 Sep;100(9):3297-303. doi: 10.1210/JC.2015-2007. Epub 2015 Jul 10. J Clin Endocrinol Metab. 2015. PMID: 26161452
Signification of distal urinary acidification defects in hypocitraturic patients.
Forni Ogna V, Blanchard A, Vargas-Poussou R, Ogna A, Baron S, Bertocchio JP, Prot-Bertoye C, Nevoux J, Dubourg J, Maruani G, Mendes M, Garcia-Castaño A, Treard C, Lepottier N, Houillier P, Courbebaisse M. Forni Ogna V, et al. Among authors: baron s. PLoS One. 2017 May 19;12(5):e0177329. doi: 10.1371/journal.pone.0177329. eCollection 2017. PLoS One. 2017. PMID: 28542241 Free PMC article.
Resistance to Insulin in Patients with Gitelman Syndrome and a Subtle Intermediate Phenotype in Heterozygous Carriers: A Cross-Sectional Study.
Blanchard A, Vallet M, Dubourg L, Hureaux M, Allard J, Haymann JP, de la Faille R, Arnoux A, Dinut A, Bergerot D, Becker PH, Courand PY, Baron S, Houillier P, Tack I, Devuyst O, Jeunemaitre X, Azizi M, Vargas-Poussou R. Blanchard A, et al. Among authors: baron s. J Am Soc Nephrol. 2019 Aug;30(8):1534-1545. doi: 10.1681/ASN.2019010031. Epub 2019 Jul 8. J Am Soc Nephrol. 2019. PMID: 31285285 Free PMC article.
Differences in the spectrum of steroidogenic enzyme inhibition between Osilodrostat and Metyrapone in ACTH-dependent Cushing syndrome patients.
Bonnet-Serrano F, Poirier J, Vaczlavik A, Laguillier-Morizot C, Blanchet B, Baron S, Guignat L, Bessiene L, Bricaire L, Groussin L, Assié G, Guibourdenche J, Bertherat J. Bonnet-Serrano F, et al. Among authors: baron s. Eur J Endocrinol. 2022 Jul 4;187(2):315-322. doi: 10.1530/EJE-22-0208. Print 2022 Aug 1. Eur J Endocrinol. 2022. PMID: 35699971
Indomethacin, amiloride, or eplerenone for treating hypokalemia in Gitelman syndrome.
Blanchard A, Vargas-Poussou R, Vallet M, Caumont-Prim A, Allard J, Desport E, Dubourg L, Monge M, Bergerot D, Baron S, Essig M, Bridoux F, Tack I, Azizi M. Blanchard A, et al. Among authors: baron s. J Am Soc Nephrol. 2015 Feb;26(2):468-75. doi: 10.1681/ASN.2014030293. Epub 2014 Jul 10. J Am Soc Nephrol. 2015. PMID: 25012174 Free PMC article. Clinical Trial.
1,212 results