Biason-Lauber A - Search Results

1

Estrogens: Two nuclear receptors, multiple possibilities.

Biason-Lauber A, Lang-Muritano M. Biason-Lauber A, et al. Mol Cell Endocrinol. 2022 Aug 20;554:111710. doi: 10.1016/j.mce.2022.111710. Epub 2022 Jul 2. Mol Cell Endocrinol. 2022. PMID: 35787463 Free article. Review.

2

Early-Onset Complete Ovarian Failure and Lack of Puberty in a Woman With Mutated Estrogen Receptor β (ESR2).

Lang-Muritano M, Sproll P, Wyss S, Kolly A, Hürlimann R, Konrad D, Biason-Lauber A. Lang-Muritano M, et al. Among authors: biason lauber a. J Clin Endocrinol Metab. 2018 Oct 1;103(10):3748-3756. doi: 10.1210/jc.2018-00769. J Clin Endocrinol Metab. 2018. PMID: 30113650

3

Aromatase deficiency owing to a functional variant in the placenta promoter and a novel missense mutation in the CYP19A1 gene.

Hauri-Hohl A, Meyer-Böni M, Lang-Muritano M, Hauri-Hohl M, Schoenle EJ, Biason-Lauber A. Hauri-Hohl A, et al. Clin Endocrinol (Oxf). 2011 Jul;75(1):39-43. doi: 10.1111/j.1365-2265.2011.04012.x. Clin Endocrinol (Oxf). 2011. PMID: 21521281

4

P450c17 deficiency: clinical and molecular characterization of six patients.

Rosa S, Duff C, Meyer M, Lang-Muritano M, Balercia G, Boscaro M, Topaloglu AK, Mioni R, Fallo F, Zuliani L, Mantero F, Schoenle EJ, Biason-Lauber A. Rosa S, et al. J Clin Endocrinol Metab. 2007 Mar;92(3):1000-7. doi: 10.1210/jc.2006-1486. Epub 2006 Dec 27. J Clin Endocrinol Metab. 2007. PMID: 17192295

5

Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 gene.

Biason-Lauber A, Lang-Muritano M, Vaccaro T, Schoenle EJ. Biason-Lauber A, et al. Diabetes. 2002 Jul;51(7):2301-5. doi: 10.2337/diabetes.51.7.2301. Diabetes. 2002. PMID: 12086964

6

A novel mutation in the anti-müllerian hormone gene as cause of persistent müllerian duct syndrome.

Lang-Muritano M, Biason-Lauber A, Gitzelmann C, Belville C, Picard Y, Schoenle EJ. Lang-Muritano M, et al. Eur J Pediatr. 2001 Nov;160(11):652-4. doi: 10.1007/s004310100840. Eur J Pediatr. 2001. PMID: 11760020

7

Clinical, genetic and functional characteristics of three novel CYP17A1 mutations causing combined 17alpha-hydroxylase/17,20-lyase deficiency.

Rosa S, Steigert M, Lang-Muritano M, l'Allemand D, Schoenle EJ, Biason-Lauber A. Rosa S, et al. Horm Res Paediatr. 2010;73(3):198-204. doi: 10.1159/000284362. Epub 2010 Mar 3. Horm Res Paediatr. 2010. PMID: 20197673 Free article.

8

Epidemiology of type I diabetes mellitus in Switzerland: steep rise in incidence in under 5 year old children in the past decade.

Schoenle EJ, Lang-Muritano M, Gschwend S, Laimbacher J, Mullis PE, Torresani T, Biason-Lauber A, Molinari L. Schoenle EJ, et al. Diabetologia. 2001 Mar;44(3):286-9. doi: 10.1007/s001250051615. Diabetologia. 2001. PMID: 11317657

9

Association of childhood type 1 diabetes mellitus with a variant of PAX4: possible link to beta cell regenerative capacity.

Biason-Lauber A, Boehm B, Lang-Muritano M, Gauthier BR, Brun T, Wollheim CB, Schoenle EJ. Biason-Lauber A, et al. Diabetologia. 2005 May;48(5):900-5. doi: 10.1007/s00125-005-1723-5. Epub 2005 Apr 15. Diabetologia. 2005. PMID: 15834548 Free article.

10

A novel mutation inducing partial androgen-insensitivity syndrome with phenotypic diversity.

Gobet R, Lang-Muritano M, Stallmach T, Biason-Lauber A. Gobet R, et al. BJU Int. 2003 Dec;92 Suppl 3:e34-e35. doi: 10.1111/j.1464-410x.2003.04030.x. BJU Int. 2003. PMID: 19125473 No abstract available.

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