Pfäffle R - Search Results

1

Thyroid - what is a healthy thyroid function test?

Kiess W, Kirstein AS, Kratzsch J, Gesing J, Pfäffle R. Kiess W, et al. Among authors: pfaffle r. J Pediatr Endocrinol Metab. 2023 Feb 14;36(3):223-224. doi: 10.1515/jpem-2023-0040. Print 2023 Mar 28. J Pediatr Endocrinol Metab. 2023. PMID: 36775974 Free article. No abstract available.

2

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. Among authors: pfaffle r. Clin Endocrinol (Oxf). 2000 May;52(5):661-5. doi: 10.1046/j.1365-2265.2000.00942.x. Clin Endocrinol (Oxf). 2000. PMID: 10792348

3

Idiopathic growth hormone deficiency: a vanishing diagnosis?

Pfäffle R, Blankenstein O, Wüller S, Heimann K, Heimann G. Pfäffle R, et al. Horm Res. 2000;53 Suppl 3:1-8. doi: 10.1159/000023524. Horm Res. 2000. PMID: 10971095 Review.

4

[Function of the hypothalamo-hypophyseal-adrenal axis to corticotropin-releasing hormone test in premature infants with bronchopulmonary dysplasia].

Merz U, Pfäffle R, Peschgens T, Hörnchen H. Merz U, et al. Among authors: pfaffle r. Z Geburtshilfe Neonatol. 1997 Nov-Dec;201(6):253-7. Z Geburtshilfe Neonatol. 1997. PMID: 9491545 Clinical Trial. German.

5

[Glucose homeostasis in cystic fibrosis. Oral glucose tolerance test in comparison with formula administration].

Skopnik H, Kentrup H, Kusenbach G, Pfäffle R, Kock R. Skopnik H, et al. Among authors: pfaffle r. Monatsschr Kinderheilkd. 1993 Jan;141(1):42-7. Monatsschr Kinderheilkd. 1993. PMID: 8446117 German.

6

Genetics of growth hormone gene expression.

Parks JS, Abdul-Latif H, Kinoshita E, Meacham LR, Pfäffle RW, Brown MR. Parks JS, et al. Among authors: pfaffle rw. Horm Res. 1993;40(1-3):54-61. doi: 10.1159/000183768. Horm Res. 1993. PMID: 8300051 Review.

7

Mutation of the POU-specific domain of Pit-1 and hypopituitarism without pituitary hypoplasia.

Pfäffle RW, DiMattia GE, Parks JS, Brown MR, Wit JM, Jansen M, Van der Nat H, Van den Brande JL, Rosenfeld MG, Ingraham HA. Pfäffle RW, et al. Science. 1992 Aug 21;257(5073):1118-21. doi: 10.1126/science.257.5073.1118. Science. 1992. PMID: 1509263

8

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.

9

GH and TSH deficiency.

Pfäffle RW, Martinez R, Kim C, Frisch H, Lebl J, Otten B, Heimann G. Pfäffle RW, et al. Exp Clin Endocrinol Diabetes. 1997;105 Suppl 4:1-5. Exp Clin Endocrinol Diabetes. 1997. PMID: 9439906

10

Familial combined pituitary hormone deficiency caused by PROP-1 gene mutation. Growth patterns and MRI studies in untreated subjects.

Crone J, Pfäffle R, Stobbe H, Prayer D, Gomez I, Frisch H. Crone J, et al. Among authors: pfaffle r. Horm Res. 2002;57(3-4):120-6. doi: 10.1159/000057962. Horm Res. 2002. PMID: 12006708

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