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Hydroxyurea in old patients with essential thrombocythemia.
Randi ML, Ruzzon E, Piccoli A, Tezza F, Scapin M, Scandellari R, Fabris F. Randi ML, et al. Among authors: scapin m. Aging Clin Exp Res. 2008 Aug;20(4):376-80. doi: 10.1007/BF03324871. Aging Clin Exp Res. 2008. PMID: 18852553
The mutant JAK2 allele burden in children with essential thrombocythemia.
Teofili L, Cenci T, Martini M, Capodimonti S, Torti L, Giona F, Amendola A, Randi ML, Putti MC, Scapin M, Leone G, Larocca LM. Teofili L, et al. Among authors: scapin m. Br J Haematol. 2009 May;145(3):430-2. doi: 10.1111/j.1365-2141.2009.07591.x. Epub 2009 Feb 4. Br J Haematol. 2009. PMID: 19208099 Free article. No abstract available.
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant.
Vettore S, Scandellari R, Moro S, Lombardi AM, Scapin M, Randi ML, Fabris F. Vettore S, et al. Among authors: scapin m. Haematologica. 2008 Nov;93(11):1743-7. doi: 10.3324/haematol.12830. Epub 2008 Sep 24. Haematologica. 2008. PMID: 18815197 Free article.
31 results