Mullis PE - Search Results

1

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: mullis pe. 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

2

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: mullis pe. 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.

3

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: mullis pe. J Endocrinol. 2000 May;165(2):313-20. doi: 10.1677/joe.0.1650313. J Endocrinol. 2000. PMID: 10810295

4

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: mullis pe. Horm Res Paediatr. 2010;73(2):140-7. doi: 10.1159/000277660. Epub 2010 Feb 9. Horm Res Paediatr. 2010. PMID: 20190552 Free article.

5

Prevalence of human GH-1 gene alterations in patients with isolated growth hormone deficiency.

Wagner JK, Eblé A, Hindmarsh PC, Mullis PE. Wagner JK, et al. Among authors: mullis pe. Pediatr Res. 1998 Jan;43(1):105-10. doi: 10.1203/00006450-199801000-00016. Pediatr Res. 1998. PMID: 9432120

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. Among authors: mullis pe. Diabetologia. 1999 Sep;42(9):1067-70. doi: 10.1007/s001250051272. Diabetologia. 1999. PMID: 10447517 Free article.

7

Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiency.

Petkovic V, Lochmatter D, Turton J, Clayton PE, Trainer PJ, Dattani MT, Eblé A, Robinson IC, Flück CE, Mullis PE. Petkovic V, et al. Among authors: mullis pe. J Clin Endocrinol Metab. 2007 Nov;92(11):4427-35. doi: 10.1210/jc.2007-0857. Epub 2007 Aug 28. J Clin Endocrinol Metab. 2007. PMID: 17726075

8

Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and action.

Petkovic V, Godi M, Pandey AV, Lochmatter D, Buchanan CR, Dattani MT, Eblé A, Flück CE, Mullis PE. Petkovic V, et al. Among authors: mullis pe. J Clin Endocrinol Metab. 2010 Feb;95(2):731-9. doi: 10.1210/jc.2009-1247. Epub 2009 Dec 1. J Clin Endocrinol Metab. 2010. PMID: 19952226

9

Use of combined liothyronine and thyroxine therapy for consumptive hypothyroidism associated with hepatic haemangiomas in infancy.

Peters C, Langham S, Mullis PE, Dattani MT. Peters C, et al. Among authors: mullis pe. Horm Res Paediatr. 2010;74(2):149-52. doi: 10.1159/000281884. Epub 2010 Jun 3. Horm Res Paediatr. 2010. PMID: 20516650 Free article.

10

BamHI RFLP for the GHRHR locus.

Cao Y, Wagner JK, Eblé A, Hindmarsh P, Mullis PE. Cao Y, et al. Among authors: mullis pe. Hum Mol Genet. 1994 Apr;3(4):682. doi: 10.1093/hmg/3.4.682. Hum Mol Genet. 1994. PMID: 7915169 No abstract available.

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