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Regulatory landscape of providing information on newborn screening to parents across Europe.
Franková V, Driscoll RO, Jansen ME, Loeber JG, Kožich V, Bonham J, Borde P, Brincat I, Cheillan D, Dekkers E, Fingerhut R, Kuš IB, Girginoudis P, Groselj U, Hougaard D, Knapková M, la Marca G, Malniece I, Nanu MI, Nennstiel U, Olkhovych N, Oltarzewski M, Pettersen RD, Racz G, Reinson K, Salimbayeva D, Songailiene J, Vilarinho L, Vogazianos M, Zetterström RH, Zeyda M; Members of the European Society of Human Genetics (ESHG)-EuroGentest Quality Sub-Committee. Franková V, et al. Among authors: girginoudis p. Eur J Hum Genet. 2021 Jan;29(1):67-78. doi: 10.1038/s41431-020-00716-6. Epub 2020 Oct 10. Eur J Hum Genet. 2021. PMID: 33040093 Free PMC article.
Global impact of COVID-19 on newborn screening programmes.
Koracin V, Loeber JG, Mlinaric M, Battelino T, Bonham JR, Groselj U; COVID-NBS ISNS global network. Koracin V, et al. BMJ Glob Health. 2022 Mar;7(3):e007780. doi: 10.1136/bmjgh-2021-007780. BMJ Glob Health. 2022. PMID: 35236661 Free PMC article.
Adrenal Steroids in Female Hypothyroid Neonates: Unraveling an Association Between Thyroid Hormones and Adrenal Remodeling.
Galanou S, Chouliaras G, Girginoudis P, Mengreli C, Sertedaki A, Dracopoulou M, Farakla I, Platis D, Iliadi A, Chrousos GP, Dacou-Voutetakis C, Zoumakis E, Magiakou AM, Kanaka-Gantenbein C, Voutetakis A. Galanou S, et al. Among authors: girginoudis p. J Clin Endocrinol Metab. 2019 Sep 1;104(9):3996-4004. doi: 10.1210/jc.2018-02013. J Clin Endocrinol Metab. 2019. PMID: 30785998
Molecular characterization of novel and rare DNA variants in patients with galactosemia.
Maroulis V, Agathangelidis A, Skouma A, Sdogou T, Papadakis MN, Papakonstantinou E, Girginoudis P, Vorgias CE, Aleporou V, Kollia P. Maroulis V, et al. Among authors: girginoudis p. Front Genet. 2023 Nov 27;14:1266353. doi: 10.3389/fgene.2023.1266353. eCollection 2023. Front Genet. 2023. PMID: 38090149 Free PMC article.