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Items: 1 to 20 of 27

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.

Hematol Rep. 2014 Mar 26;6(1):4996. doi: 10.4081/hr.2014.4996. eCollection 2014 Jan 29.

2.

Cardiovascular events and intensity of treatment in polycythemia vera.

Marchioli R, Finazzi G, Specchia G, Cacciola R, Cavazzina R, Cilloni D, De Stefano V, Elli E, Iurlo A, Latagliata R, Lunghi F, Lunghi M, Marfisi RM, Musto P, Masciulli A, Musolino C, Cascavilla N, Quarta G, Randi ML, Rapezzi D, Ruggeri M, Rumi E, Scortechini AR, Santini S, Scarano M, Siragusa S, Spadea A, Tieghi A, Angelucci E, Visani G, Vannucchi AM, Barbui T; CYTO-PV Collaborative Group.

N Engl J Med. 2013 Jan 3;368(1):22-33. doi: 10.1056/NEJMoa1208500. Epub 2012 Dec 8.

3.

Epidemiology of primary and secondary thrombocytopenia: first analysis of an administrative database in a major Italian institution.

Galdarossa M, Vianello F, Tezza F, Allemand E, Treleani M, Scarparo P, Fabris F.

Blood Coagul Fibrinolysis. 2012 Jun;23(4):271-7. doi: 10.1097/MBC.0b013e328351882d.

PMID:
22343688
4.

A A386G biallelic GPIb╬▒ 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.

Haematologica. 2011 Dec;96(12):1878-82. doi: 10.3324/haematol.2010.039008. Epub 2011 Oct 11.

5.

A 40-year-old man with recurrent fainting, hypotension, lower limb edema and oliguria with body weight gain and secondary erythrocytosis.

Berti de Marinis G, Bertozzi I, Allemand E, Tezza F, Randi ML, Naso A, Fabris F.

Intern Emerg Med. 2012 Oct;7(5):453-6. Epub 2011 Sep 25. No abstract available.

PMID:
21948352
6.

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.

Aging Clin Exp Res. 2011 Feb;23(1):17-21.

PMID:
21499015
7.

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.

Acta Haematol. 2010;123(3):140-5. doi: 10.1159/000280466. Epub 2010 Feb 4.

PMID:
20134155
8.

Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature.

Girolami A, Tezza F, Scandellari R, Vettore S, Girolami B.

J Thromb Thrombolysis. 2010 Aug;30(2):172-8. doi: 10.1007/s11239-009-0435-y. Review.

PMID:
20044773
9.

Rectus muscle sheath haematoma in a patient with congenital FX deficiency and in another with congenital FVII deficiency.

Girolami A, Allemand E, Tezza F, Pellati D, Scandellari R.

Haemophilia. 2010 Jan;16(1):182-5. doi: 10.1111/j.1365-2516.2009.02091.x. Epub 2009 Oct 29. No abstract available.

PMID:
19878333
10.

Hydroxyurea in old patients with essential thrombocythemia.

Randi ML, Ruzzon E, Piccoli A, Tezza F, Scapin M, Scandellari R, Fabris F.

Aging Clin Exp Res. 2008 Aug;20(4):376-80.

PMID:
18852553
11.

Arterial thrombosis and drospirenone-containing pill (Yasmin). Is the pill to be absolutely avoided by women who smoke?

Girolami A, Tezza F, Allemand E, Girolami B.

J Thromb Thrombolysis. 2008 Oct;26(2):163-4. Epub 2007 Dec 23. No abstract available.

PMID:
18157712
12.

Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature.

Girolami A, Ruzzon E, Tezza F, Scandellari R, Scapin M, Scarparo P.

Haemophilia. 2008 Mar;14(2):323-8. Epub 2007 Dec 10. Review.

PMID:
18081833
13.

Haemostatic proteins gene polymorphisms in patients with unusual vein thrombosis and Ph-myeloproliferative disorders.

Randi ML, Lombardi AM, Scapin M, Tezza F, Scandellari R, Ruzzon E, Duner E, Fabris F.

Thromb Haemost. 2007 Sep;98(3):702-4. No abstract available.

PMID:
17849070
14.

Retinal central artery occlusion in a young woman after ten days of a drospirenone-containing oral contraceptive (Yasmin).

Girolami A, Vettore S, Tezza F, Girolami B.

Thromb Haemost. 2007 Aug;98(2):473-4. No abstract available.

PMID:
17721635
15.

Previous thrombosis-free pregnancies are no guarantee that subsequent oral contraception may also remain asymptomatic.

Girolami A, Scandellari R, Spiezia L, Tezza F.

J Thromb Thrombolysis. 2008 Aug;26(1):62-3. Epub 2007 Jun 30. No abstract available.

PMID:
17602282
16.

Increased risk of pregnancy complications in patients with essential thrombocythemia carrying the JAK2 (617V>F) mutation.

Passamonti F, Randi ML, Rumi E, Pungolino E, Elena C, Pietra D, Scapin M, Arcaini L, Tezza F, Moratti R, Pascutto C, Fabris F, Morra E, Cazzola M, Lazzarino M.

Blood. 2007 Jul 15;110(2):485-9. Epub 2007 Apr 10.

17.

Arterial thrombosis in young women after ovarian stimulation: case report and review of the literature.

Girolami A, Scandellari R, Tezza F, Paternoster D, Girolami B.

J Thromb Thrombolysis. 2007 Oct;24(2):169-74. Epub 2007 Jan 30. Review.

PMID:
17265135
18.

Congenital combined defects of factor VII: a critical review.

Girolami A, Ruzzon E, Tezza F, Allemand E, Vettore S.

Acta Haematol. 2007;117(1):51-6. Epub 2006 Nov 8. Review.

PMID:
17095860
19.

Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review.

Girolami A, Ruzzon E, Tezza F, Scandellari R, Vettore S, Girolami B.

Haemophilia. 2006 Jul;12(4):345-51. Review.

PMID:
16834733
20.

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.

Aging Clin Exp Res. 2006 Jun;18(3):187-90. Review.

PMID:
16804363

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