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Flora Peyvandi

Showing results (281-290 of 610) with videos related to

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Blood Cells, Molecules & Diseases|May 10, 2003
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patientsLuciano Baronciani, Giovanna Cozzi, Maria Teresa Canciani, et al.
Human Mutation|December 26, 2003
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiencyFlora Peyvandi, Liliana Tagliabue, Marzia Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 19, 2022
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia ASilvia Spena, Andrea Cairo, Emanuela Pappalardo, et al.
Annals of Hematology|November 20, 2019
Atypical primary cutaneous cryptococcosis during ibrutinib therapy for chronic lymphocytic leukemiaAnna Maria Peri, Raffaella Rossio, Francesco Tafuri, et al.
Blood Transfusion = Trasfusione Del Sangue|February 5, 2024
Evaluation of an automated platelet aggregation method for detection of congenital or acquired platelet function defectsAnna Lecchi, Marco Capecchi, Lidia Padovan, et al.
Research and Practice in Thrombosis and Haemostasis|August 21, 2023
Erratum to 'A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays.' [Research and Practice in Thrombosis and Haemostasis Volume 7, Issue 3, March 2023, 100139]Paola Colpani, Luciano Baronciani, Francesca Stufano, et al.
Blood Reviews|May 24, 2021
Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiencyFlora Peyvandi, Guenter Auerswald, Steven K Austin, et al.
Human Mutation|February 3, 2006
Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activityFlora Peyvandi, Silvia Lavoretano, Roberta Palla, et al.
Thrombosis Research|September 17, 2024
Main features of ischemic stroke in patients with acute immune-mediated thrombotic thrombocytopenic purpuraAddolorata Truma, Ilaria Mancini, Pasquale Agosti, et al.
British Journal of Haematology|May 26, 2012
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathiesMarie Scully, Beverley J Hunt, Sylvia Benjamin, et al.
Pageof 61

Showing results (281-290 of 610) with videos related to

Sort By:
Pageof 61
Blood Cells, Molecules & Diseases|May 10, 2003
Molecular defects in type 3 von Willebrand disease: updated results from 40 multiethnic patientsLuciano Baronciani, Giovanna Cozzi, Maria Teresa Canciani, et al.
Human Mutation|December 26, 2003
Phenotype-genotype characterization of 10 families with severe a subunit factor XIII deficiencyFlora Peyvandi, Liliana Tagliabue, Marzia Menegatti, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 19, 2022
Genetic variants at the chromosomal region 2q21.3 underlying inhibitor development in patients with severe haemophilia ASilvia Spena, Andrea Cairo, Emanuela Pappalardo, et al.
Annals of Hematology|November 20, 2019
Atypical primary cutaneous cryptococcosis during ibrutinib therapy for chronic lymphocytic leukemiaAnna Maria Peri, Raffaella Rossio, Francesco Tafuri, et al.
Blood Transfusion = Trasfusione Del Sangue|February 5, 2024
Evaluation of an automated platelet aggregation method for detection of congenital or acquired platelet function defectsAnna Lecchi, Marco Capecchi, Lidia Padovan, et al.
Research and Practice in Thrombosis and Haemostasis|August 21, 2023
Erratum to 'A comparative study in type 2 von Willebrand disease patients using four different platelet-dependent von Willebrand factor assays.' [Research and Practice in Thrombosis and Haemostasis Volume 7, Issue 3, March 2023, 100139]Paola Colpani, Luciano Baronciani, Francesca Stufano, et al.
Blood Reviews|May 24, 2021
Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiencyFlora Peyvandi, Guenter Auerswald, Steven K Austin, et al.
Human Mutation|February 3, 2006
Mechanisms of the interaction between two ADAMTS13 gene mutations leading to severe deficiency of enzymatic activityFlora Peyvandi, Silvia Lavoretano, Roberta Palla, et al.
Thrombosis Research|September 17, 2024
Main features of ischemic stroke in patients with acute immune-mediated thrombotic thrombocytopenic purpuraAddolorata Truma, Ilaria Mancini, Pasquale Agosti, et al.
British Journal of Haematology|May 26, 2012
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathiesMarie Scully, Beverley J Hunt, Sylvia Benjamin, et al.
Pageof 61