Flück C - Search Results

1

Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C).

Flück C, Deladoey J, Rutishauser K, Eblé A, Marti U, Wu W, Mullis PE. Flück C, et al. J Clin Endocrinol Metab. 1998 Oct;83(10):3727-34. doi: 10.1210/jcem.83.10.5172. J Clin Endocrinol Metab. 1998. PMID: 9768691

2

"Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.

Deladoëy J, Flück C, Büyükgebiz A, Kuhlmann BV, Eblé A, Hindmarsh PC, Wu W, Mullis PE. Deladoëy J, et al. Among authors: fluck c. J Clin Endocrinol Metab. 1999 May;84(5):1645-50. doi: 10.1210/jcem.84.5.5681. J Clin Endocrinol Metab. 1999. PMID: 10323394

3

Aromatase deficiency caused by a novel P450arom gene mutation: impact of absent estrogen production on serum gonadotropin concentration in a boy.

Deladoëy J, Flück C, Bex M, Yoshimura N, Harada N, Mullis PE. Deladoëy J, et al. Among authors: fluck c. J Clin Endocrinol Metab. 1999 Nov;84(11):4050-4. doi: 10.1210/jcem.84.11.6135. J Clin Endocrinol Metab. 1999. PMID: 10566648

4

Regulation of human GH receptor gene transcription by 20 and 22 kDa GH in a human hepatoma cell line.

Nuoffer JM, Flück C, Deladoëy J, Eblé A, Dattani MT, Mullis PE. Nuoffer JM, et al. Among authors: fluck c. J Endocrinol. 2000 May;165(2):313-20. doi: 10.1677/joe.0.1650313. J Endocrinol. 2000. PMID: 10810295

5

Autosomal dominant neurohypophyseal diabetes insipidus in a Swiss family, caused by a novel mutation (C59Delta/A60W) in the neurophysin moiety of prepro-vasopressin-neurophysin II (AVP-NP II).

Flück CE, Deladoëy J, Nayak S, Zeller O, Kopp P, Mullis PE. Flück CE, et al. Eur J Endocrinol. 2001 Oct;145(4):439-44. doi: 10.1530/eje.0.1450439. Eur J Endocrinol. 2001. PMID: 11581002

6

Insulin increases serum leptin concentrations in children and adolescents with newly diagnosed type I diabetes mellitus with and without ketoacidosis.

Flück CE, Kuhlmann BV, Mullis PE. Flück CE, et al. Diabetologia. 1999 Sep;42(9):1067-70. doi: 10.1007/s001250051272. Diabetologia. 1999. PMID: 10447517 Free article.

7

Insulin-like growth factor-I treatment in primary growth hormone insensitivity: effect of recombinant human IGF-I (rhIGF-I) and rhIGF-I/rhIGF-binding protein-3 complex.

Tonella P, Flück CE, Mullis PE. Tonella P, et al. Among authors: fluck ce. Horm Res Paediatr. 2010;73(2):140-7. doi: 10.1159/000277660. Epub 2010 Feb 9. Horm Res Paediatr. 2010. PMID: 20190552 Free article.

8

Ten novel mutations in the NR5A1 gene cause disordered sex development in 46,XY and ovarian insufficiency in 46,XX individuals.

Camats N, Pandey AV, Fernández-Cancio M, Andaluz P, Janner M, Torán N, Moreno F, Bereket A, Akcay T, García-García E, Muñoz MT, Gracia R, Nistal M, Castaño L, Mullis PE, Carrascosa A, Audí L, Flück CE. Camats N, et al. Among authors: fluck ce. J Clin Endocrinol Metab. 2012 Jul;97(7):E1294-306. doi: 10.1210/jc.2011-3169. Epub 2012 May 1. J Clin Endocrinol Metab. 2012. PMID: 22549935 Free article.

9

Do centimetres matter? Self-reported versus estimated height measurements in parents.

Gozzi T, Flück C, L'allemand D, Dattani MT, Hindmarsh PC, Mullis PE. Gozzi T, et al. Among authors: fluck c. Acta Paediatr. 2010 Apr;99(4):569-74. doi: 10.1111/j.1651-2227.2009.01654.x. Epub 2009 Dec 24. Acta Paediatr. 2010. PMID: 20050829

10

[Metabolic control in children and adolescents with diabetes mellitus type I in Berne: a cross-sectional study].

Flück CE, Kuhlmann BV, Mullis PE. Flück CE, et al. Schweiz Med Wochenschr. 1999 Nov 6;129(44):1650-5. Schweiz Med Wochenschr. 1999. PMID: 10588023 German.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

210 results

Search Page

Filters