Flück C - Search Results

1

SNP array profiling of childhood adrenocortical tumors reveals distinct pathways of tumorigenesis and highlights candidate driver genes.

Letouzé E, Rosati R, Komechen H, Doghman M, Marisa L, Flück C, de Krijger RR, van Noesel MM, Mas JC, Pianovski MA, Zambetti GP, Figueiredo BC, Lalli E. Letouzé E, et al. Among authors: fluck c. J Clin Endocrinol Metab. 2012 Jul;97(7):E1284-93. doi: 10.1210/jc.2012-1184. Epub 2012 Apr 26. J Clin Endocrinol Metab. 2012. PMID: 22539591

2

A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of Swiss ancestry with congenital lipoid adrenal hyperplasia.

Flück CE, Maret A, Mallet D, Portrat-Doyen S, Achermann JC, Leheup B, Theintz GE, Mullis PE, Morel Y. Flück CE, et al. J Clin Endocrinol Metab. 2005 Sep;90(9):5304-8. doi: 10.1210/jc.2005-0874. Epub 2005 Jun 28. J Clin Endocrinol Metab. 2005. PMID: 15985476 Free article.

3

Risk of Meningioma in European Patients Treated With Growth Hormone in Childhood: Results From the SAGhE Cohort.

Swerdlow AJ, Cooke R, Beckers D, Butler G, Carel JC, Cianfarani S, Clayton P, Coste J, Deodati A, Ecosse E, Hokken-Koelega ACS, Khan AJ, Kiess W, Kuehni CE, Flück CE, Pfaffle R, Sävendahl L, Sommer G, Thomas M, Tidblad A, Tollerfield S, Zandwijken GRJ. Swerdlow AJ, et al. Among authors: fluck ce. J Clin Endocrinol Metab. 2019 Mar 1;104(3):658-664. doi: 10.1210/jc.2018-01133. J Clin Endocrinol Metab. 2019. PMID: 30137467 Free PMC article.

4

Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and stature.

Petkovic V, Besson A, Thevis M, Lochmatter D, Eblé A, Flück CE, Mullis PE. Petkovic V, et al. J Clin Endocrinol Metab. 2007 Aug;92(8):2893-901. doi: 10.1210/jc.2006-2238. Epub 2007 May 22. J Clin Endocrinol Metab. 2007. PMID: 17519310

5

Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiency.

Räz B, Janner M, Petkovic V, Lochmatter D, Eblé A, Dattani MT, Hindmarsh PC, Flück CE, Mullis PE. Räz B, et al. Among authors: fluck ce. J Clin Endocrinol Metab. 2008 Mar;93(3):974-80. doi: 10.1210/jc.2007-1382. Epub 2007 Nov 20. J Clin Endocrinol Metab. 2008. PMID: 18029459 Free article.

6

Normal hepatic glycogen storage after fasting and feeding in children and adolescents with type 1 diabetes.

Flück CE, Slotboom J, Nuoffer JM, Kreis R, Boesch C, Mullis PE. Flück CE, et al. Pediatr Diabetes. 2003 Jun;4(2):70-6. doi: 10.1034/j.1399-5448.2003.00015.x. Pediatr Diabetes. 2003. PMID: 14655262

7

Short stature caused by a biologically inactive mutant growth hormone (GH-C53S).

Besson A, Salemi S, Deladoëy J, Vuissoz JM, Eblé A, Bidlingmaier M, Bürgi S, Honegger U, Flück C, Mullis PE. Besson A, et al. Among authors: fluck c. J Clin Endocrinol Metab. 2005 May;90(5):2493-9. doi: 10.1210/jc.2004-1838. Epub 2005 Feb 15. J Clin Endocrinol Metab. 2005. PMID: 15713716

8

Genetic testing for glucokinase mutations in clinically selected patients with MODY: a worthwhile investment.

Schnyder S, Mullis PE, Ellard S, Hattersley AT, Flück CE. Schnyder S, et al. Swiss Med Wkly. 2005 Jun 11;135(23-24):352-6. doi: 10.4414/smw.2005.11030. Swiss Med Wkly. 2005. PMID: 16059790 Free article.

9

Clinical and biochemical description of a novel CYP21A2 gene mutation 962_963insA using a new 3D model for the P450c21 protein.

Janner M, Pandey AV, Mullis PE, Flück CE. Janner M, et al. Eur J Endocrinol. 2006 Jul;155(1):143-51. doi: 10.1530/eje.1.02172. Eur J Endocrinol. 2006. PMID: 16793961

10

Leydig-cell tumour in children: variable clinical presentation, diagnostic features, follow-up and genetic analysis of four cases.

Petkovic V, Salemi S, Vassella E, Karamitopoulou-Diamantis E, Meinhardt UJ, Flück CE, Mullis PE. Petkovic V, et al. Horm Res. 2007;67(2):89-95. doi: 10.1159/000096356. Epub 2006 Oct 17. Horm Res. 2007. PMID: 17047343

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