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F Rodeghiero

Showing results (161-170 of 266) with videos related to

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Acta Haematologica|January 1, 1987
Recurrent life-threatening epistaxis in a child with Bernard-Soulier syndrome controlled by bilateral ligation of external carotids and ethmoidal arteriesF Rodeghiero, G Castaman, G Pesavento, et al.
Blood|May 16, 1998
Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression systemN Takahashi, H Tsukamoto, H Umeyama, et al.
Leukemia|February 16, 2007
Un-mutated IgVH in chronic lymphocytic leukemia is associated with a higher risk of immune thrombocytopeniaC Visco, I Giaretta, M Ruggeri, et al.
Blut|July 1, 1987
Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy. Report of a second caseF Rodeghiero, G C Castaman, E Di Bona, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 1, 1990
Incidence and risk factors for thrombotic complications in a historical cohort of 100 patients with essential thrombocythemiaS Cortelazzo, P Viero, G Finazzi, et al.
Thrombosis Research|July 15, 1990
Platelet von Willebrand factor assay: results using two methods for platelet lysisF Rodeghiero, G C Castaman, A Tosetto, et al.
British Journal of Haematology|January 29, 2000
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutationG Castaman, J C Eikenboom, A Lattuada, et al.
Seminars in Thrombosis and Hemostasis|January 1, 1996
ETRO Working Party on Factor XIII questionnaire on congenital factor XIII deficiency in Europe: status and perspectives. Study GroupR Seitz, F Duckert, S Lopaciuk, et al.
American Journal of Hematology|August 1, 1995
Platelet von Willebrand factor abnormalities in myeloproliferative syndromesG Castaman, A Lattuada, M Ruggeri, et al.
Thrombosis and Haemostasis|May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian originJ C Eikenboom, G Castaman, H L Vos, et al.
Pageof 27

Showing results (161-170 of 266) with videos related to

Sort By:
Pageof 27
Acta Haematologica|January 1, 1987
Recurrent life-threatening epistaxis in a child with Bernard-Soulier syndrome controlled by bilateral ligation of external carotids and ethmoidal arteriesF Rodeghiero, G Castaman, G Pesavento, et al.
Blood|May 16, 1998
Molecular mechanisms of type II factor XIII deficiency: novel Gly562-Arg mutation and C-terminal truncation of the A subunit cause factor XIII deficiency as characterized in a mammalian expression systemN Takahashi, H Tsukamoto, H Umeyama, et al.
Leukemia|February 16, 2007
Un-mutated IgVH in chronic lymphocytic leukemia is associated with a higher risk of immune thrombocytopeniaC Visco, I Giaretta, M Ruggeri, et al.
Blut|July 1, 1987
Successful pregnancy in a woman with congenital factor XIII deficiency treated with substitutive therapy. Report of a second caseF Rodeghiero, G C Castaman, E Di Bona, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|March 1, 1990
Incidence and risk factors for thrombotic complications in a historical cohort of 100 patients with essential thrombocythemiaS Cortelazzo, P Viero, G Finazzi, et al.
Thrombosis Research|July 15, 1990
Platelet von Willebrand factor assay: results using two methods for platelet lysisF Rodeghiero, G C Castaman, A Tosetto, et al.
British Journal of Haematology|January 29, 2000
Heightened proteolysis of the von Willebrand factor subunit in patients with von Willebrand disease hemizygous or homozygous for the C2362F mutationG Castaman, J C Eikenboom, A Lattuada, et al.
Seminars in Thrombosis and Hemostasis|January 1, 1996
ETRO Working Party on Factor XIII questionnaire on congenital factor XIII deficiency in Europe: status and perspectives. Study GroupR Seitz, F Duckert, S Lopaciuk, et al.
American Journal of Hematology|August 1, 1995
Platelet von Willebrand factor abnormalities in myeloproliferative syndromesG Castaman, A Lattuada, M Ruggeri, et al.
Thrombosis and Haemostasis|May 6, 1998
Characterization of the genetic defects in recessive type 1 and type 3 von Willebrand disease patients of Italian originJ C Eikenboom, G Castaman, H L Vos, et al.
Pageof 27