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Four globin gene defects in a healthy child.
Badens C, Merono F, Martini N, Lena-Russo D, Gulbis B, Thuret I. Badens C, et al. Among authors: gulbis b. Haematologica. 2002 Nov;87(11):ELT42. Haematologica. 2002. PMID: 12414363 No abstract available.
Newborn Screening for Sickle Cell Disease in Europe.
Daniel Y, Elion J, Allaf B, Badens C, Bouva MJ, Brincat I, Cela E, Coppinger C, de Montalembert M, Gulbis B, Henthorn J, Ketelslegers O, McMahon C, Streetly A, Colombatti R, Lobitz S. Daniel Y, et al. Among authors: gulbis b. Int J Neonatal Screen. 2019 Feb 12;5(1):15. doi: 10.3390/ijns5010015. eCollection 2019 Mar. Int J Neonatal Screen. 2019. PMID: 33072975 Free PMC article. Review.
Haemoglobinopathies in Europe: health & migration policy perspectives.
Aguilar Martinez P, Angastiniotis M, Eleftheriou A, Gulbis B, Mañú Pereira Mdel M, Petrova-Benedict R, Corrons JL. Aguilar Martinez P, et al. Among authors: gulbis b. Orphanet J Rare Dis. 2014 Jul 1;9:97. doi: 10.1186/1750-1172-9-97. Orphanet J Rare Dis. 2014. PMID: 24980780 Free PMC article.
Newborn screening for sickle cell disease in Europe: recommendations from a Pan-European Consensus Conference.
Lobitz S, Telfer P, Cela E, Allaf B, Angastiniotis M, Backman Johansson C, Badens C, Bento C, Bouva MJ, Canatan D, Charlton M, Coppinger C, Daniel Y, de Montalembert M, Ducoroy P, Dulin E, Fingerhut R, Frömmel C, García-Morin M, Gulbis B, Holtkamp U, Inusa B, James J, Kleanthous M, Klein J, Kunz JB, Langabeer L, Lapouméroulie C, Marcao A, Marín Soria JL, McMahon C, Ohene-Frempong K, Périni JM, Piel FB, Russo G, Sainati L, Schmugge M, Streetly A, Tshilolo L, Turner C, Venturelli D, Vilarinho L, Yahyaoui R, Elion J, Colombatti R; with the endorsement of EuroBloodNet, the European Reference Network in Rare Haematological Diseases. Lobitz S, et al. Among authors: gulbis b. Br J Haematol. 2018 Nov;183(4):648-660. doi: 10.1111/bjh.15600. Epub 2018 Oct 18. Br J Haematol. 2018. PMID: 30334577 Free article.
192 results