Mullis PE - Search Results

1

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. Among authors: mullis pe. Horm Res. 2007;67(2):89-95. doi: 10.1159/000096356. Epub 2006 Oct 17. Horm Res. 2007. PMID: 17047343

2

The aromatase cytochrome P-450 and its clinical impact.

Meinhardt U, Mullis PE. Meinhardt U, et al. Among authors: mullis pe. Horm Res. 2002;57(5-6):145-52. doi: 10.1159/000058374. Horm Res. 2002. PMID: 12053085 Review.

3

Autosomal-dominant isolated growth hormone deficiency (IGHD type II) with normal GH-1 gene.

Fintini D, Salvatori R, Salemi S, Otten B, Ubertini G, Cambiaso P, Mullis PE. Fintini D, et al. Among authors: mullis pe. Horm Res. 2006;65(2):76-82. doi: 10.1159/000091033. Epub 2006 Jan 18. Horm Res. 2006. PMID: 16424673

4

Impact of del32-71-GH (exon 3 skipped GH) on intracellular GH distribution, secretion and cell viability: a quantitative confocal microscopy analysis.

Salemi S, Yousefi S, Eblé A, Deladoëy J, Mullis PE. Salemi S, et al. Among authors: mullis pe. Horm Res. 2006;65(3):132-41. doi: 10.1159/000091607. Epub 2006 Feb 17. Horm Res. 2006. PMID: 16491012

5

A novel GH-1 gene mutation (GH-P59L) causes partial GH deficiency type II combined with bioinactive GH syndrome.

Petkovic V, Eblé A, Pandey AV, Betta M, Mella P, Flück CE, Buzi F, Mullis PE. Petkovic V, et al. Among authors: mullis pe. Growth Horm IGF Res. 2011 Jun;21(3):160-6. doi: 10.1016/j.ghir.2011.04.002. Epub 2011 May 4. Growth Horm IGF Res. 2011. PMID: 21546299

6

Impact of estrogen replacement throughout childhood on growth, pituitary-gonadal axis and bone in a 46,XX patient with CYP19A1 deficiency.

Janner M, Flück CE, Mullis PE. Janner M, et al. Among authors: mullis pe. Horm Res Paediatr. 2012;78(4):261-8. doi: 10.1159/000341585. Epub 2012 Sep 6. Horm Res Paediatr. 2012. PMID: 22964562 Free article.

7

Acute encephalopathy with unilateral cortical-subcortical lesions in two unrelated kindreds treated with glucocorticoids prenatally for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: established facts and novel insight.

Grunt S, Steinlin M, Weisstanner C, Schöning M, Mullis PE, Flück CE. Grunt S, et al. Among authors: mullis pe. Horm Res Paediatr. 2013;80(1):57-63. doi: 10.1159/000348515. Epub 2013 Jun 29. Horm Res Paediatr. 2013. PMID: 23816834 Free article.

8

The role of zinc dynamics in growth hormone secretion.

Miletta MC, Schöni MH, Kernland K, Mullis PE, Petkovic V. Miletta MC, et al. Among authors: mullis pe. Horm Res Paediatr. 2013;80(6):381-9. doi: 10.1159/000355408. Epub 2013 Nov 26. Horm Res Paediatr. 2013. PMID: 24296719 Free article. Review.

9

New N-terminal located mutation (Q4ter) within the POU1F1-gene (PIT-1) causes recessive combined pituitary hormone deficiency and variable phenotype.

Salemi S, Besson A, Eblé A, Gallati S, Pfäffle RW, Mullis PE. Salemi S, et al. Among authors: mullis pe. Growth Horm IGF Res. 2003 Oct;13(5):264-8. doi: 10.1016/s1096-6374(03)00015-7. Growth Horm IGF Res. 2003. PMID: 12932747

10

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.

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