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Page 1
Thyroid disorders revisited.
Kiess W, Penke M, Gesing J, Hoppmann J, Müller E, Körner A, Kratzsch J, Pfaeffle R. Kiess W, et al. Among authors: gesing j. J Pediatr Endocrinol Metab. 2015 Jul;28(7-8):731-3. doi: 10.1515/jpem-2015-0251. J Pediatr Endocrinol Metab. 2015. PMID: 26167975 Free article. No abstract available.
Serum irisin levels are regulated by acute strenuous exercise.
Löffler D, Müller U, Scheuermann K, Friebe D, Gesing J, Bielitz J, Erbs S, Landgraf K, Wagner IV, Kiess W, Körner A. Löffler D, et al. Among authors: gesing j. J Clin Endocrinol Metab. 2015 Apr;100(4):1289-99. doi: 10.1210/jc.2014-2932. Epub 2015 Jan 27. J Clin Endocrinol Metab. 2015. PMID: 25625801 Clinical Trial.
Direct evidence of brown adipocytes in different fat depots in children.
Rockstroh D, Landgraf K, Wagner IV, Gesing J, Tauscher R, Lakowa N, Kiess W, Bühligen U, Wojan M, Till H, Blüher M, Körner A. Rockstroh D, et al. Among authors: gesing j. PLoS One. 2015 Feb 23;10(2):e0117841. doi: 10.1371/journal.pone.0117841. eCollection 2015. PLoS One. 2015. PMID: 25706927 Free PMC article.
Turner syndrome - working together with patients and their families.
Kiess W, Penke M, Gorski T, Körner A, Hoppmann J, Müller E, Gesing J, Pfaeffle R. Kiess W, et al. Among authors: gesing j. J Pediatr Endocrinol Metab. 2015 Nov 1;28(11-12):1199-201. doi: 10.1515/jpem-2015-0411. J Pediatr Endocrinol Metab. 2015. PMID: 26536580 No abstract available.
Puberty - genes, environment and clinical issues.
Kiess W, Hoppmann J, Gesing J, Penke M, Körner A, Kratzsch J, Pfaeffle R. Kiess W, et al. Among authors: gesing j. J Pediatr Endocrinol Metab. 2016 Nov 1;29(11):1229-1231. doi: 10.1515/jpem-2016-0394. J Pediatr Endocrinol Metab. 2016. PMID: 27771625 Free article. No abstract available.
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: gesing j. 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.
Phenotypic Variability in a Family with Acrodysostosis Type 2 Caused by a Novel PDE4D Mutation Affecting the Serine Target of Protein Kinase-A Phosphorylation.
Hoppmann J, Gesing J, Silve C, Leroy C, Bertsche A, Hirsch FW, Kiess W, Pfäffle R, Schuster V. Hoppmann J, et al. Among authors: gesing j. J Clin Res Pediatr Endocrinol. 2017 Dec 15;9(4):360-365. doi: 10.4274/jcrpe.4488. Epub 2017 May 17. J Clin Res Pediatr Endocrinol. 2017. PMID: 28515031 Free PMC article.
18 results