Scandellari R - Search Results

1

Serum Thrombopoietin and cMpl Expression in Thrombocytopenia of Different Etiologies.

Vianello F, Vettore S, Tezza F, Toni LD, Scandellari R, Sambado L, Treleani M, Fabris F. Vianello F, et al. Among authors: scandellari r. Hematol Rep. 2014 Mar 26;6(1):4996. doi: 10.4081/hr.2014.4996. eCollection 2014 Jan 29. Hematol Rep. 2014. PMID: 24711916 Free PMC article.

2

A A386G biallelic GPIbα gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis.

Vettore S, Tezza F, Malara A, Vianello F, Pecci A, Scandellari R, Floris M, Balduini A, Fabris F. Vettore S, et al. Among authors: scandellari r. Haematologica. 2011 Dec;96(12):1878-82. doi: 10.3324/haematol.2010.039008. Epub 2011 Oct 11. Haematologica. 2011. PMID: 21993687 Free PMC article. Clinical Trial.

3

Leg ulcers in elderly on hydroxyurea: a single center experience in Ph- myeloproliferative disorders and review of literature.

Ruzzon E, Randi ML, Tezza F, Luzzatto G, Scandellari R, Fabris F. Ruzzon E, et al. Among authors: scandellari r. Aging Clin Exp Res. 2006 Jun;18(3):187-90. doi: 10.1007/BF03324647. Aging Clin Exp Res. 2006. PMID: 16804363 Review.

4

A case of Bernard-Soulier Syndrome due to a homozygous four bases deletion (TGAG) of GPIbalpha gene: lack of GPIbalpha but absence of bleeding.

Vettore S, Scandellari R, Scapin M, Lombardi AM, Duner E, Randi ML, Fabris F. Vettore S, et al. Among authors: scandellari r. Platelets. 2008 Aug;19(5):388-91. doi: 10.1080/09537100801949976. Platelets. 2008. PMID: 18791947

5

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: scandellari r. Aging Clin Exp Res. 2008 Aug;20(4):376-80. doi: 10.1007/BF03324871. Aging Clin Exp Res. 2008. PMID: 18852553

6

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: scandellari r. Haematologica. 2008 Nov;93(11):1743-7. doi: 10.3324/haematol.12830. Epub 2008 Sep 24. Haematologica. 2008. PMID: 18815197 Free article.

7

Platelet response to Helicobacter pylori eradication therapy in adult chronic idiopathic thrombocytopenic purpura seems to be related to the presence of anticytotoxin-associated gene A antibodies.

Scandellari R, Allemand E, Vettore S, Plebani M, Randi ML, Fabris F. Scandellari R, et al. Blood Coagul Fibrinolysis. 2009 Mar;20(2):108-13. doi: 10.1097/MBC.0b013e32832315d8. Blood Coagul Fibrinolysis. 2009. PMID: 19786938

8

A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect.

Vettore S, De Rocco D, Gerber B, Scandellari R, Bianco AM, Balduini CL, Pecci A, Fabris F, Savoia A. Vettore S, et al. Among authors: scandellari r. Eur J Med Genet. 2010 Sep-Oct;53(5):256-60. doi: 10.1016/j.ejmg.2010.06.010. Epub 2010 Jul 21. Eur J Med Genet. 2010. PMID: 20603234

9

JAK2V617F mutation is common in old patients with polycythemia vera and essential thrombocythemia.

Randi ML, Ruzzon E, Tezza F, Scapin M, Duner E, Scandellari R, Fabris F. Randi ML, et al. Among authors: scandellari r. Aging Clin Exp Res. 2011 Feb;23(1):17-21. doi: 10.1007/BF03324948. Aging Clin Exp Res. 2011. PMID: 21499015

10

Heparin-induced thrombocytopenia in patients with Philadelphia-negative myeloproliferative disorders and unusual splanchnic or cerebral vein thrombosis.

Randi ML, Tezza F, Scapin M, Duner E, Scarparo P, Scandellari R, Fabris F. Randi ML, et al. Among authors: scandellari r. Acta Haematol. 2010;123(3):140-5. doi: 10.1159/000280466. Epub 2010 Feb 4. Acta Haematol. 2010. PMID: 20134155

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