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Maternal uniparental disomy of chromosome 4 and homozygous novel mutation in the WFS1 gene in a paediatric patient with Wolfram syndrome.
Papadimitriou DT, Manolakos E, Bothou C, Zoupanos G, Papoulidis I, Orru S, Skarmoutsos F, Delides A, Bakoula C, Papadimitriou A, Urano F. Papadimitriou DT, et al. Among authors: papadimitriou a. Diabetes Metab. 2015 Nov;41(5):433-5. doi: 10.1016/j.diabet.2015.06.003. Epub 2015 Jul 10. Diabetes Metab. 2015. PMID: 26169481 No abstract available.
Secular changes in the final height of Greek girls are levelling off.
Kleanthous K, Dermitzaki E, Papadimitriou DT, Papaevangelou V, Papadimitriou A. Kleanthous K, et al. Among authors: papadimitriou dt, papadimitriou a. Acta Paediatr. 2017 Feb;106(2):341-343. doi: 10.1111/apa.13677. Epub 2016 Dec 19. Acta Paediatr. 2017. PMID: 27859729 No abstract available.
Replacement of Male Mini-Puberty.
Papadimitriou DT, Chrysis D, Nyktari G, Zoupanos G, Liakou E, Papadimitriou A, Mastorakos G. Papadimitriou DT, et al. Among authors: papadimitriou a. J Endocr Soc. 2019 May 9;3(7):1275-1282. doi: 10.1210/js.2019-00083. eCollection 2019 Jul 1. J Endocr Soc. 2019. PMID: 31240270 Free PMC article.
A novel detrimental homozygous mutation in the WFS1 gene in two sisters from nonconsanguineous parents with untreated diabetes insipidus.
Papadimitriou DT, Kleanthous K, Manolakos E, Tiulpakov A, Nikolopoulos T, Delides A, Voros G, Dinopoulos A, Zoupanos G, Papadimitriou A, Mastorakos G, Urano F. Papadimitriou DT, et al. Among authors: papadimitriou a. Clin Case Rep. 2019 Oct 23;7(12):2355-2357. doi: 10.1002/ccr3.2494. eCollection 2019 Dec. Clin Case Rep. 2019. PMID: 31893057 Free PMC article.
67 results