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Eva Zetterberg

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Histopathology|January 19, 2012
A novel immunohistochemical sequential multi-labelling and erasing technique enables epitope characterization of bone marrow pericytes in primary myelofibrosisAnn Madelung, Michael Bzorek, Henrik Bondo, et al.
Journal of Thrombosis and Haemostasis : JTH|February 2, 2023
Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disordersCarlo Zaninetti, Eva Leinøe, María Luisa Lozano, et al.
AIDS (London, England)|September 29, 2012
Platelet count kinetics following interruption of antiretroviral treatmentEva Zetterberg, Jacqueline Neuhaus, Jason V Baker, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 8, 2020
Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen-related genesMarcus Fager Ferrari, Eva Zetterberg, Maria Rossing, et al.
Frontiers in Immunology|December 3, 2021
Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in <i>GNE</i>Karolina I Smolag, Marcus Fager Ferrari, Eva Zetterberg, et al.
Haematologica|May 10, 2007
Pericyte coverage of abnormal blood vessels in myelofibrotic bone marrowsEva Zetterberg, Alessandro M Vannucchi, Anna Rita Migliaccio, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 27, 2020
Genetic screening of children with suspected inherited bleeding disordersNadine G Andersson, Maria Rossing, Marcus Fager Ferrari, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 5, 2019
Evaluation of a standardized protocol for thrombin generation using the calibrated automated thrombogram: A Nordic studyMarcus Ljungkvist, Karin Strandberg, Erik Berntorp, et al.
Journal of Thrombosis and Haemostasis : JTH|August 1, 2021
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in DenmarkEva Leinøe, Nanna Brøns, Andreas Ørslev Rasmussen, et al.
British Journal of Haematology|December 21, 2022
Acquired Haemophilia A in four north European countries: survey of 181 patientsRickard Lindahl, Vuokko Nummi, Anna-Elina Lehtinen, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
Histopathology|January 19, 2012
A novel immunohistochemical sequential multi-labelling and erasing technique enables epitope characterization of bone marrow pericytes in primary myelofibrosisAnn Madelung, Michael Bzorek, Henrik Bondo, et al.
Journal of Thrombosis and Haemostasis : JTH|February 2, 2023
Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disordersCarlo Zaninetti, Eva Leinøe, María Luisa Lozano, et al.
AIDS (London, England)|September 29, 2012
Platelet count kinetics following interruption of antiretroviral treatmentEva Zetterberg, Jacqueline Neuhaus, Jason V Baker, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 8, 2020
Collagen remodelling and plasma ascorbic acid levels in patients suspected of inherited bleeding disorders harbouring germline variants in collagen-related genesMarcus Fager Ferrari, Eva Zetterberg, Maria Rossing, et al.
Frontiers in Immunology|December 3, 2021
Severe Congenital Thrombocytopenia Characterized by Decreased Platelet Sialylation and Moderate Complement Activation Caused by Novel Compound Heterozygous Variants in <i>GNE</i>Karolina I Smolag, Marcus Fager Ferrari, Eva Zetterberg, et al.
Haematologica|May 10, 2007
Pericyte coverage of abnormal blood vessels in myelofibrotic bone marrowsEva Zetterberg, Alessandro M Vannucchi, Anna Rita Migliaccio, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 27, 2020
Genetic screening of children with suspected inherited bleeding disordersNadine G Andersson, Maria Rossing, Marcus Fager Ferrari, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 5, 2019
Evaluation of a standardized protocol for thrombin generation using the calibrated automated thrombogram: A Nordic studyMarcus Ljungkvist, Karin Strandberg, Erik Berntorp, et al.
Journal of Thrombosis and Haemostasis : JTH|August 1, 2021
The Copenhagen founder variant GP1BA c.58T>G is the most frequent cause of inherited thrombocytopenia in DenmarkEva Leinøe, Nanna Brøns, Andreas Ørslev Rasmussen, et al.
British Journal of Haematology|December 21, 2022
Acquired Haemophilia A in four north European countries: survey of 181 patientsRickard Lindahl, Vuokko Nummi, Anna-Elina Lehtinen, et al.
Pageof 5