Pfaffle R - Search Results

1

Cancer Risks in Patients Treated With Growth Hormone in Childhood: The SAGhE European Cohort Study.

Swerdlow AJ, Cooke R, Beckers D, Borgström B, Butler G, Carel JC, Cianfarani S, Clayton P, Coste J, Deodati A, Ecosse E, Gausche R, Giacomozzi C, Hokken-Koelega ACS, Khan AJ, Kiess W, Kuehni CE, Mullis PE, Pfaffle R, Sävendahl L, Sommer G, Thomas M, Tidblad A, Tollerfield S, Van Eycken L, Zandwijken GRJ. Swerdlow AJ, et al. Among authors: pfaffle r. J Clin Endocrinol Metab. 2017 May 1;102(5):1661-1672. doi: 10.1210/jc.2016-2046. J Clin Endocrinol Metab. 2017. PMID: 28187225 Free PMC article.

2

Genetics and molecular biology in short stature.

Mullis PE, Argente J, Amselem S, Pfäffle R, van der Burgt I. Mullis PE, et al. Among authors: pfaffle r. Acta Paediatr Suppl. 1995 Sep;411:75-80. doi: 10.1111/j.1651-2227.1995.tb13869.x. Acta Paediatr Suppl. 1995. PMID: 8563074 No abstract available.

3

Adrenocorticotrope deficiency with clinical evidence for late onset in combined pituitary hormone deficiency caused by a homozygous 301-302delAG mutation of the PROP1 gene.

Lamesch C, Neumann S, Pfäffle R, Kiess W, Paschke R. Lamesch C, et al. Among authors: pfaffle r. Pituitary. 2002;5(3):163-8. doi: 10.1023/a:1023356915458. Pituitary. 2002. PMID: 12812307

4

PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis.

Böttner A, Keller E, Kratzsch J, Stobbe H, Weigel JF, Keller A, Hirsch W, Kiess W, Blum WF, Pfäffle RW. Böttner A, et al. J Clin Endocrinol Metab. 2004 Oct;89(10):5256-65. doi: 10.1210/jc.2004-0661. J Clin Endocrinol Metab. 2004. PMID: 15472232

5

Comparison of adrenal function tests in children--the glucagon stimulation test allows the simultaneous assessment of adrenal function and growth hormone response in children.

Böttner A, Kratzsch J, Liebermann S, Keller A, Pfaffle RW, Kiess W, Keller E. Böttner A, et al. J Pediatr Endocrinol Metab. 2005 May;18(5):433-42. doi: 10.1515/jpem.2005.18.5.433. J Pediatr Endocrinol Metab. 2005. PMID: 15921172 Clinical Trial.

6

A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome.

Raile K, Stobbe H, Tröbs RB, Kiess W, Pfäffle R. Raile K, et al. Among authors: pfaffle r. Eur J Endocrinol. 2005 Sep;153(3):353-8. doi: 10.1530/eje.1.01974. Eur J Endocrinol. 2005. PMID: 16131596

7

Clinical and functional characteristics of the human Arg59Ter insulin-like growth factor i receptor (IGF1R) mutation: implications for a gene dosage effect of the human IGF1R.

Raile K, Klammt J, Schneider A, Keller A, Laue S, Smith R, Pfäffle R, Kratzsch J, Keller E, Kiess W. Raile K, et al. Among authors: pfaffle r. J Clin Endocrinol Metab. 2006 Jun;91(6):2264-71. doi: 10.1210/jc.2005-2146. Epub 2006 Mar 28. J Clin Endocrinol Metab. 2006. PMID: 16569742

8

[Results of an endocrinological follow-up of patients with childhood-or adolescent-onset malignancies].

Keller A, Bierbach U, Mieke J, Pfäffle R, Kratzsch J, Kiess W, Keller E, Körholz D. Keller A, et al. Among authors: pfaffle r. Klin Padiatr. 2007 Nov-Dec;219(6):333-8. doi: 10.1055/s-2007-971045. Klin Padiatr. 2007. PMID: 18050043 Review. German.

9

IGF signaling defects as causes of growth failure and IUGR.

Klammt J, Pfäffle R, Werner H, Kiess W. Klammt J, et al. Among authors: pfaffle r. Trends Endocrinol Metab. 2008 Aug;19(6):197-205. doi: 10.1016/j.tem.2008.03.003. Trends Endocrinol Metab. 2008. PMID: 18515143 Review.

10

A prismatic case: A 31-year old man who did not miss his pituitary.

Petzold S, Keller A, Keller E, Meigen C, Hirsch W, Kratzsch JK, Kiess W, Pfäffle R. Petzold S, et al. Among authors: pfaffle r. Hormones (Athens). 2008 Jul-Sep;7(3):263-70. doi: 10.14310/horm.2002.1207. Hormones (Athens). 2008. PMID: 18694867 Free article.

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