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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.
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
31 results