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Number of items: 9.

Lang-Muritano, Mariarosaria; Sproll, Patrick; Wyss, Sascha; Kolly, Anne; Hürlimann, Renate; Konrad, Daniel; Biason-Lauber, Anna (2018). Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2). Journal of Clinical Endocrinology & Metabolism, 103(10):3748-3756.

Gerster, Karine; Katschnig, Claudia; Wyss, Sascha; Kolly, A; Sproll, P; Biason-Lauber, Anna; Konrad, Daniel (2017). A novel DAX-1 (NR0B1) mutation in a boy with X-linked adrenal hypoplasia congenita. Journal of Pediatric Endocrinology & Metabolism, 12(30):1321-1325.

Gerster, Karine; Biason-Lauber, Anna; Schoenle, Eugen J (2017). Clinical follow-up of the first SF-1 insufficient female patient. Annales d'endocrinologie, 78(3):156-161.

Ghisleni, Carmen; Bollmann, Steffen; Biason-Lauber, Anna; Poil, Simon-Shlomo; Brandeis, Daniel; Martin, Ernst; Michels, Lars; Hersberger, Martin; Suckling, John; Klaver, Peter; O'Gorman, Ruth L (2015). Effects of Steroid Hormones on Sex Differences in Cerebral Perfusion. PLoS ONE, 10(9):e0135827.

Eid, Wassim; Opitz, Lennart; Biason-Lauber, Anna (2015). Genome-wide identification of CBX2 targets: insights in the human sex development network. Molecular Endocrinology, 29(2):247-257.

Biason-Lauber, Anna; Böni-Schnetzler, Marianne; Hubbard, Basil P; Bouzakri, Karim; Brunner, Andrea; Cavelti-Weder, Claudia; Keller, Cornelia; Meyer-Böni, Monika; Meier, Daniel T; Brorsson, Caroline; Timper, Katharina; Leibowitz, Gil; Patrignani, Andrea; Bruggmann, Remy; Boily, Gino; Zulewski, Henryk; Geier, Andreas; Cermak, Jennifer M; Elliott, Peter; Ellis, James L; Westphal, Christoph; Knobel, Urs; Eloranta, Jyrki J; Kerr-Conte, Julie; Pattou, François; Konrad, Daniel; Matter, Christian M; Fontana, Adriano; Rogler, Gerhard; Schlapbach, Ralph; Regairaz, Camille; Carballido, José M; Glaser, Benjamin; McBurney, Michael W; Pociot, Flemming; Sinclair, David A; Donath, Marc Y (2013). Identification of a SIRT1 mutation in a family with type 1 Diabetes. Cell Metabolism, 17(3):448-455.

Torresani, T; Biason-Lauber, Anna (2007). Erratum: Congenital adrenal hyperplasia: diagnostic advances. Journal of Inherited Metabolic Disease, 30(5):832.

Torresani, T; Biason-Lauber, Anna (2007). Congenital adrenal hyperplasia: diagnostic advances. Journal of Inherited Metabolic Disease, 30(4):563-575.

Biason-Lauber, Anna; De Filippo, G; Konrad, D; Scarano, G; Nazzaro, A; Schoenle, EJ (2007). WNT4 deficiency—a clinical phenotype distinct from the classic Mayer–Rokitansky–Kuster–Hauser syndrome: a case report. Human Reproduction, 22(1):224-229.

This list was generated on Sat Jun 15 23:12:06 2019 CEST.