Frisch H - Search Results

1

SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.

Binder G, Renz A, Martinez A, Keselman A, Hesse V, Riedl SW, Häusler G, Fricke-Otto S, Frisch H, Heinrich JJ, Ranke MB. Binder G, et al. Among authors: frisch h. J Clin Endocrinol Metab. 2004 Sep;89(9):4403-8. doi: 10.1210/jc.2004-0591. J Clin Endocrinol Metab. 2004. PMID: 15356038

2

Effects of growth hormone (GH) and insulin-like growth factor-I therapy in patients with gene defects in the GH axis.

Riedl S, Frisch H. Riedl S, et al. Among authors: frisch h. J Pediatr Endocrinol Metab. 2006 Mar;19(3):229-36. doi: 10.1515/jpem.2006.19.3.229. J Pediatr Endocrinol Metab. 2006. PMID: 16607923

3

Long-term treatment in children with hypopituitarism: pubertal development and final height.

Birnbacher R, Riedl S, Frisch H. Birnbacher R, et al. Among authors: frisch h. Horm Res. 1998;49(2):80-5. doi: 10.1159/000023131. Horm Res. 1998. PMID: 9485176 Clinical Trial.

4

Treatment of peripubertal children after renal transplantation (RTX) with recombinant human growth hormone: auxological data and effects on insulin-like growth factor-I (IGF-I) and IGF-binding protein-3 (IGFBP-3) during 24 months.

Riedl S, Lebl J, Kluge M, Kreisinger J, Simková E, Kohlhauser C, Balzar E, Frisch H. Riedl S, et al. Among authors: frisch h. J Pediatr Endocrinol Metab. 1998 Nov-Dec;11(6):713-8. doi: 10.1515/jpem.1998.11.6.713. J Pediatr Endocrinol Metab. 1998. PMID: 9829225

5

Combined pituitary hormone deficiency and pituitary hypoplasia due to a mutation of the Pit-1 gene.

Frisch H, Kim C, Häusler G, Pfäffle R. Frisch H, et al. Clin Endocrinol (Oxf). 2000 May;52(5):661-5. doi: 10.1046/j.1365-2265.2000.00942.x. Clin Endocrinol (Oxf). 2000. PMID: 10792348

6

Posterior pituitary ectopy in children with idiopathic growth hormone deficiency.

Mészáros F, Vergesslich K, Riedl S, Häusler G, Frisch H. Mészáros F, et al. Among authors: frisch h. J Pediatr Endocrinol Metab. 2000 Jun;13(6):629-35. doi: 10.1515/jpem.2000.13.6.629. J Pediatr Endocrinol Metab. 2000. PMID: 10905387

7

Adaptation of ghrelin and the GH/IGF axis to high altitude.

Riedl S, Kluge M, Schweitzer K, Waldhör T, Frisch H. Riedl S, et al. Among authors: frisch h. Eur J Endocrinol. 2012 Jun;166(6):969-76. doi: 10.1530/EJE-12-0007. Epub 2012 Mar 13. Eur J Endocrinol. 2012. PMID: 22416077

8

Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous states.

Fang P, Riedl S, Amselem S, Pratt KL, Little BM, Haeusler G, Hwa V, Frisch H, Rosenfeld RG. Fang P, et al. Among authors: frisch h. J Clin Endocrinol Metab. 2007 Jun;92(6):2223-31. doi: 10.1210/jc.2006-2624. Epub 2007 Apr 3. J Clin Endocrinol Metab. 2007. PMID: 17405847

9

Validation of a mathematical model predicting the response to growth hormone treatment in prepubertal children with idiopathic growth hormone deficiency.

Vosahlo J, Zidek T, Lebl J, Riedl S, Frisch H. Vosahlo J, et al. Among authors: frisch h. Horm Res. 2004;61(3):143-7. doi: 10.1159/000075590. Epub 2003 Dec 15. Horm Res. 2004. PMID: 14676463

10

Spontaneous growth in idiopathic short stature. European Study Group.

Rekers-Mombarg LT, Wit JM, Massa GG, Ranke MB, Buckler JM, Butenandt O, Chaussain JL, Frisch H, Leiberman E. Rekers-Mombarg LT, et al. Among authors: frisch h. Arch Dis Child. 1996 Sep;75(3):175-80. doi: 10.1136/adc.75.3.175. Arch Dis Child. 1996. PMID: 8976652 Free PMC article.

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