Vettore S - Search Results

1

Presence of anti-ADAMTS13 antibodies in obesity.

Lombardi AM, Fabris R, Scarda A, Zanato V, Dal Prà C, Scarparo P, Vettore S, Granzotto M, Berti De Marinis G, Foletto M, Serra R, Sartori MT, Plebani M, Fabris F, Vettor R. Lombardi AM, et al. Among authors: vettore s. Eur J Clin Invest. 2012 Nov;42(11):1197-204. doi: 10.1111/j.1365-2362.2012.02710.x. Epub 2012 Sep 8. Eur J Clin Invest. 2012. PMID: 22957496

2

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. Among authors: vettore s. Blood Coagul Fibrinolysis. 2009 Mar;20(2):108-13. doi: 10.1097/MBC.0b013e32832315d8. Blood Coagul Fibrinolysis. 2009. PMID: 19786938

3

Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era.

Girolami A, Vettore S, Scarparo P, Lombardi AM. Girolami A, et al. Among authors: vettore s. Haemophilia. 2011 Jan;17(1):17-20. doi: 10.1111/j.1365-2516.2010.02328.x. Haemophilia. 2011. PMID: 20546029

4

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

5

Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard-Soulier syndrome.

Girolami A, Vettore S, Vianello F, Berti de Marinis G, Fabris F. Girolami A, et al. Among authors: vettore s. J Thromb Thrombolysis. 2012 Nov;34(4):513-7. doi: 10.1007/s11239-012-0742-6. J Thromb Thrombolysis. 2012. PMID: 22569901

6

Unexplained discrepancies in the activity--antigen ratio in congenital FX deficiencies with defects in the catalytic domain.

Girolami A, Scarparo P, Vettore S, Candeo N, Scandellari R, Lombardi AM. Girolami A, et al. Among authors: vettore s. Clin Appl Thromb Hemost. 2009 Dec;15(6):621-7. doi: 10.1177/1076029609343447. Epub 2009 Aug 9. Clin Appl Thromb Hemost. 2009. PMID: 19666942 Free article. Review.

7

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. Platelets. 2008 Aug;19(5):388-91. doi: 10.1080/09537100801949976. Platelets. 2008. PMID: 18791947

8

Determinants of plasma levels of plasminogen activator inhibitor-1 : A study of normotensive twins.

Cesari M, Sartori MT, Patrassi GM, Vettore S, Rossi GP. Cesari M, et al. Among authors: vettore s. Arterioscler Thromb Vasc Biol. 1999 Feb;19(2):316-20. doi: 10.1161/01.atv.19.2.316. Arterioscler Thromb Vasc Biol. 1999. PMID: 9974413

9

Congenital FVII deficiency and pulmonary embolism: a critical appraisal of all reported cases.

Girolami A, Berti de Marinis G, Vettore S, Girolami B. Girolami A, et al. Among authors: vettore s. Clin Appl Thromb Hemost. 2013 Jan-Feb;19(1):55-9. doi: 10.1177/1076029611436196. Epub 2012 Feb 12. Clin Appl Thromb Hemost. 2013. PMID: 22327818 Free article. Review.

10

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. 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

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