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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 myelofibrosis
Ann 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 disorders
Carlo Zaninetti, Eva Leinøe, María Luisa Lozano, et al.
AIDS (London, England)
|
September 29, 2012
Platelet count kinetics following interruption of antiretroviral treatment
Eva 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 genes
Marcus 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 marrows
Eva 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 disorders
Nadine 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 study
Marcus 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 Denmark
Eva 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 patients
Rickard Lindahl, Vuokko Nummi, Anna-Elina Lehtinen, et al.
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of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Histopathology
|
January 19, 2012
A novel immunohistochemical sequential multi-labelling and erasing technique enables epitope characterization of bone marrow pericytes in primary myelofibrosis
Ann 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 disorders
Carlo Zaninetti, Eva Leinøe, María Luisa Lozano, et al.
AIDS (London, England)
|
September 29, 2012
Platelet count kinetics following interruption of antiretroviral treatment
Eva 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 genes
Marcus 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 marrows
Eva 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 disorders
Nadine 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 study
Marcus 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 Denmark
Eva 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 patients
Rickard Lindahl, Vuokko Nummi, Anna-Elina Lehtinen, et al.
Page
of 5