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Page 1
Mass pre-embryo adoption.
Demartis F. Demartis F. Camb Q Healthc Ethics. 1998 Winter;7(1):101-3. doi: 10.1017/s0963180198701136. Camb Q Healthc Ethics. 1998. PMID: 9523048 No abstract available.
KLF1 gene mutations cause borderline HbA(2).
Perseu L, Satta S, Moi P, Demartis FR, Manunza L, Sollaino MC, Barella S, Cao A, Galanello R. Perseu L, et al. Among authors: demartis fr. Blood. 2011 Oct 20;118(16):4454-8. doi: 10.1182/blood-2011-04-345736. Epub 2011 Aug 5. Blood. 2011. PMID: 21821711 Free article.
A genetic score for the prediction of beta-thalassemia severity.
Danjou F, Francavilla M, Anni F, Satta S, Demartis FR, Perseu L, Manca M, Sollaino MC, Manunza L, Mereu E, Marceddu G, Pissard S, Joly P, Thuret I, Origa R, Borg J, Forni GL, Piga A, Lai ME, Badens C, Moi P, Galanello R. Danjou F, et al. Among authors: demartis fr. Haematologica. 2015 Apr;100(4):452-7. doi: 10.3324/haematol.2014.113886. Epub 2014 Dec 5. Haematologica. 2015. PMID: 25480500 Free PMC article.
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation.
Satta S, Paglietti ME, Sollaino MC, Barella S, Moi P, Desogus MF, Demartis FR, Manunza L, Origa R. Satta S, et al. Among authors: demartis fr. Blood Cells Mol Dis. 2017 May;64:30-32. doi: 10.1016/j.bcmd.2017.03.007. Epub 2017 Mar 18. Blood Cells Mol Dis. 2017. PMID: 28342932
Intracranial Haemorrhage in Haemophilia Patients Is Still an Open Issue: The Final Results of the Italian EMO.REC Registry.
Zanon E, Pasca S, Demartis F, Tagliaferri A, Santoro C, Cantori I, Molinari AC, Biasoli C, Coppola A, Luciani M, Sottilotta G, Ricca I, Pollio B, Borchiellini A, Tosetto A, Peyvandi F, Frigo AC, Simioni P. Zanon E, et al. Among authors: demartis f. J Clin Med. 2022 Apr 1;11(7):1969. doi: 10.3390/jcm11071969. J Clin Med. 2022. PMID: 35407576 Free PMC article.
21 results