Search Results - "Gianniello, F."

Hemostatic abnormalities in patients with Ehlers–Danlos syndrome by Artoni, A., Bassotti, A., Abbattista, M., Marinelli, B., Lecchi, A., Gianniello, F., Clerici, M., Bucciarelli, P., La Marca, S., Peyvandi, F., Martinelli, I.

“…Essentials Ehlers‐Danlos Syndrome (EDS) is a rare heterogeneous group of inherited collagen disorders. A cohort of EDS patients was investigated for bleeding…”
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Low borderline plasma levels of antithrombin, protein C and protein S are risk factors for venous thromboembolism by BUCCIARELLI, P., PASSAMONTI, S. M., BIGUZZI, E., GIANNIELLO, F., FRANCHI, F., MANNUCCI, P. M., MARTINELLI, I.

“…Background:  Inherited deficiencies of antithrombin (AT), protein C (PC) and protein S (PS) are risk factors for venous thromboembolism (VTE). They are usually…”
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Pregnancy outcome after a first episode of cerebral vein thrombosis: reply by Martinelli, I., Abbattista, M., Somigliana, E., Gianniello, F., Peyvandi, F.

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Pregnancy outcome after a first episode of cerebral vein thrombosis by Martinelli, I., Passamonti, S. M., Maino, A., Abbattista, M., Bucciarelli, P., Somigliana, E., Artoni, A., Gianniello, F., Peyvandi, F.

“…Essentials Little is known about recurrences and pregnancy outcome after cerebral vein thrombosis (CVT). We studied a cohort of pregnant women with CVT. Women…”
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The JAK2 V617F mutation in patients with cerebral venous thrombosis by PASSAMONTI, S. M., BIGUZZI, E., CAZZOLA, M., FRANCHI, F., GIANNIELLO, F., BUCCIARELLI, P., PIETRA, D., MANNUCCI, P. M., MARTINELLI, I.

“…Background:  It is currently unclear whether or not cerebral venous thrombosis, such as splanchnic venous thrombosis, can be the first manifestation of an…”
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An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees by KUNICKI, T. J., BARONCIANI, L., CANCIANI, M. T., GIANNIELLO, F., HEAD, S. R., MONDALA, T. S., SALOMON, D. R., FEDERICI, A. B.

“…We analyzed the association of bleeding severity with candidate gene haplotypes within pedigrees of 11 index cases of von Willebrand disease (VWD) type 2 (two…”
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PB0500 Edoxaban for Acute and Long-Term Treatment of Venous Thromboembolism: Real-Life Data from a Single Center Cohort Study by Abbattista, M., Capecchi, M., Barbullushi, K., Cassanello, G., Truma, A., Gianniello, F., Artoni, A., Scimeca, B., Bucciarelli, P., Peyvandi, F.

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ORIGINAL ARTICLE: An association of candidate gene haplotypes and bleeding severity in von Willebrand disease type 2A, 2B, and 2M pedigrees by Kunicki, T J, Baronciani, L, Canciani, M T, Gianniello, F, Head, SR, Mondala, T S, Salomon, DR, Federici, AB

“…We analyzed the association of bleeding severity with candidate gene haplotypes within pedigrees of 11 index cases of von Willebrand disease (VWD) type 2 (two…”
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