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Page 1
HNF1A gene mutations and premature ovarian failure (POF): evidence from a clinical paradigm combining MODY 3 and POF.
Xekouki P, Konstantinidou A, Tatsi C, Sertedaki A, Settas N, Loutradis D, Chrousos GP, Kanaka-Gantenbein C, Dacou-Voutetakis C, Voutetakis A. Xekouki P, et al. Among authors: voutetakis a. Hormones (Athens). 2024 Jun;23(2):345-350. doi: 10.1007/s42000-024-00529-y. Epub 2024 Feb 5. Hormones (Athens). 2024. PMID: 38311659 Free PMC article. Review.
Assessing the Respect of Children's Rights in Pediatric Hospitals.
Georgousopoulou V, Voutetakis A, Galanis P, Kourti FE, Zartaloudi A, Koutelekos I, Dousis E, Kosmidis D, Koutsouki S, Pappa D, Igoumenidis M, Dafogianni C. Georgousopoulou V, et al. Among authors: voutetakis a. Medicina (Kaunas). 2023 May 16;59(5):955. doi: 10.3390/medicina59050955. Medicina (Kaunas). 2023. PMID: 37241187 Free PMC article.
The Impact of the ENDORSE Digital Weight Management Program on the Metabolic Profile of Children and Adolescents with Overweight and Obesity and on Food Parenting Practices.
Pervanidou P, Chatzidaki E, Nicolaides NC, Voutetakis A, Polychronaki N, Chioti V, Kitani RA, Kyrkopoulou E, Zarkogianni K, Kalafatis E, Mitsis K, Perakis Κ, Nikita K, Kanaka-Gantenbein C. Pervanidou P, et al. Among authors: voutetakis a. Nutrients. 2023 Apr 5;15(7):1777. doi: 10.3390/nu15071777. Nutrients. 2023. PMID: 37049618 Free PMC article.
The ENDORSE Feasibility Study: Exploring the Use of M-Health, Artificial Intelligence and Serious Games for the Management of Childhood Obesity.
Zarkogianni K, Chatzidaki E, Polychronaki N, Kalafatis E, Nicolaides NC, Voutetakis A, Chioti V, Kitani RA, Mitsis K, Perakis Κ, Athanasiou M, Antonopoulou D, Pervanidou P, Kanaka-Gantenbein C, Nikita K. Zarkogianni K, et al. Among authors: voutetakis a. Nutrients. 2023 Mar 17;15(6):1451. doi: 10.3390/nu15061451. Nutrients. 2023. PMID: 36986180 Free PMC article.
Pituitary stalk interruption syndrome.
Voutetakis A. Voutetakis A. Handb Clin Neurol. 2021;181:9-27. doi: 10.1016/B978-0-12-820683-6.00002-6. Handb Clin Neurol. 2021. PMID: 34238482 Review.
Correction: Genomic and sequence variants of protein kinase A regulatory subunit type 1β (PRKAR1B) in patients with adrenocortical disease and Cushing syndrome.
Drougat L, Settas N, Ronchi CL, Bathon K, Calebiro D, Maria AG, Haydar S, Voutetakis A, London E, Faucz FR, Stratakis CA. Drougat L, et al. Among authors: voutetakis a. Genet Med. 2021 Jan;23(1):239. doi: 10.1038/s41436-020-01018-4. Genet Med. 2021. PMID: 33082560 Free article. No abstract available.
68 results