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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 2
1993 4
1995 1
1996 1
1997 3
1998 3
1999 4
2000 3
2001 2
2002 2
2003 4
2004 4
2005 3
2006 2
2007 5
2008 2
2010 5
2011 10
2012 5
2013 11
2014 4
2015 8
2016 2
2017 9
2018 9
2019 5
2020 6
2021 4
2022 5
2023 5
2024 3

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121 results

Results by year

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Page 1
Congenital hypothyroidism.
Kiess W, Penke M, Gesing J, Stoltze A, Körner A, Pfäffle R, Kratzsch J. Kiess W, et al. Among authors: pfaffle r. J Pediatr Endocrinol Metab. 2018 Jun 27;31(6):595-596. doi: 10.1515/jpem-2018-0197. J Pediatr Endocrinol Metab. 2018. PMID: 29804102 Free article. No abstract available.
GH and IGF-1 Replacement in Children.
Pfäffle R, Kiess W. Pfäffle R, et al. Handb Exp Pharmacol. 2020;261:67-86. doi: 10.1007/164_2019_337. Handb Exp Pharmacol. 2020. PMID: 31932988 Review.
Pediatric endocrinology is pediatrics is public health.
Kiess W, Penke M, Kratzsch J, Vogel M, Kapellen T, Hoppmann J, Gesing J, Gausche R, Klamt S, Körner A, Pfäffle R. Kiess W, et al. Among authors: pfaffle r. J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):371-374. doi: 10.1515/jpem-2017-0109. J Pediatr Endocrinol Metab. 2017. PMID: 28358715 Free article. No abstract available.
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.
Downstream insulin-like growth factor.
Pfäffle R, Kiess W, Klammt J. Pfäffle R, et al. Endocr Dev. 2012;23:42-51. doi: 10.1159/000341745. Epub 2012 Nov 23. Endocr Dev. 2012. PMID: 23182819 Review.
Growth hormone and growth hormone deficiency--still a lot to learn.
Kiess W, Penke M, Pfäffle R, Körner A, Kratzsch J. Kiess W, et al. Among authors: pfaffle r. J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):971-3. doi: 10.1515/jpem-2015-0321. J Pediatr Endocrinol Metab. 2015. PMID: 26353173 No abstract available.
IGF1R mutations as cause of SGA.
Klammt J, Kiess W, Pfäffle R. Klammt J, et al. Among authors: pfaffle r. Best Pract Res Clin Endocrinol Metab. 2011 Feb;25(1):191-206. doi: 10.1016/j.beem.2010.09.012. Best Pract Res Clin Endocrinol Metab. 2011. PMID: 21396585 Review.
Genetics of Growth Disorders-Which Patients Require Genetic Testing?
Argente J, Tatton-Brown K, Lehwalder D, Pfäffle R. Argente J, et al. Among authors: pfaffle r. Front Endocrinol (Lausanne). 2019 Sep 6;10:602. doi: 10.3389/fendo.2019.00602. eCollection 2019. Front Endocrinol (Lausanne). 2019. PMID: 31555216 Free PMC article. Review.
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.
121 results