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Journal of Thrombosis and Haemostasis : JTH
|
February 19, 2021
Severe thrombophilia in a factor V-deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)
Elisabetta Castoldi, Nathalie Hézard, Guillaume Mourey, et al.
Journal of Thrombosis and Haemostasis : JTH
|
April 21, 2023
Single-cell analysis of megakaryopoiesis in peripheral CD34<sup>+</sup> cells: insights into ETV6-related thrombocytopenia
Timothée Bigot, Elisa Gabinaud, Laurent Hannouche, et al.
Atherosclerosis
|
December 27, 2019
High prevalence of mutations in perilipin 1 in patients with precocious acute coronary syndrome
Nathalie Bonello-Palot, Marc Laine, Thomas Cuisset, et al.
Plos Genetics
|
January 19, 2021
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
Pierre-Emmanuel Morange, Franck Peiretti, Lenaick Gourhant, et al.
Healthcare (Basel, Switzerland)
|
October 27, 2022
Challenges Associated with Effective Implementation of CT Dose Check Standards and Radiation Monitoring Index in Computed Tomography: Healthcare Sector Experience
Entesar Zawam Dalah, Yousuf Mohammad Al Musfari, Badriya Mohd Hassan Ali, et al.
Journal of Thrombosis and Haemostasis : JTH
|
November 1, 2024
High risk of long-term recurrence after a first episode of venous thromboembolism during pregnancy or postpartum: the REcurrence after a PrEgnAncy related Thrombosis (REPEAT) Study
Manal Ibrahim-Kosta, Sarah El Harake, Barbara Leclercq, et al.
Scientific Reports
|
July 8, 2021
An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism
Misbah Razzaq, Maria Jesus Iglesias, Manal Ibrahim-Kosta, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 5, 2024
Plasma levels of complement components C5 and C9 are associated with thrombin generation
Rocío Vacik Díaz, Gaëlle Munsch, Maria Jesus Iglesias, et al.
Haematologica
|
January 2, 2025
FLI1 and GATA1 govern <i>TLN1</i> transcription: new insights into FLI1-related platelet disorders
Elisa Gabinaud, Laurent Hannouche, Mathilde Veneziano-Broccia, et al.
Research and Practice in Thrombosis and Haemostasis
|
March 9, 2026
Platelet dense granule defect: experience in the French population
Delphine Borgel, Agathe Beauvais, Cécile Bally, et al.
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of 7
Search research articles
Search
Showing results (51-60 of 68) with videos related to
Sort By:
Page
of 7
Journal of Thrombosis and Haemostasis : JTH
|
February 19, 2021
Severe thrombophilia in a factor V-deficient patient homozygous for the Ala2086Asp mutation (FV Besançon)
Elisabetta Castoldi, Nathalie Hézard, Guillaume Mourey, et al.
Journal of Thrombosis and Haemostasis : JTH
|
April 21, 2023
Single-cell analysis of megakaryopoiesis in peripheral CD34<sup>+</sup> cells: insights into ETV6-related thrombocytopenia
Timothée Bigot, Elisa Gabinaud, Laurent Hannouche, et al.
Atherosclerosis
|
December 27, 2019
High prevalence of mutations in perilipin 1 in patients with precocious acute coronary syndrome
Nathalie Bonello-Palot, Marc Laine, Thomas Cuisset, et al.
Plos Genetics
|
January 19, 2021
A rare coding mutation in the MAST2 gene causes venous thrombosis in a French family with unexplained thrombophilia: The Breizh MAST2 Arg89Gln variant
Pierre-Emmanuel Morange, Franck Peiretti, Lenaick Gourhant, et al.
Healthcare (Basel, Switzerland)
|
October 27, 2022
Challenges Associated with Effective Implementation of CT Dose Check Standards and Radiation Monitoring Index in Computed Tomography: Healthcare Sector Experience
Entesar Zawam Dalah, Yousuf Mohammad Al Musfari, Badriya Mohd Hassan Ali, et al.
Journal of Thrombosis and Haemostasis : JTH
|
November 1, 2024
High risk of long-term recurrence after a first episode of venous thromboembolism during pregnancy or postpartum: the REcurrence after a PrEgnAncy related Thrombosis (REPEAT) Study
Manal Ibrahim-Kosta, Sarah El Harake, Barbara Leclercq, et al.
Scientific Reports
|
July 8, 2021
An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism
Misbah Razzaq, Maria Jesus Iglesias, Manal Ibrahim-Kosta, et al.
Journal of Thrombosis and Haemostasis : JTH
|
June 5, 2024
Plasma levels of complement components C5 and C9 are associated with thrombin generation
Rocío Vacik Díaz, Gaëlle Munsch, Maria Jesus Iglesias, et al.
Haematologica
|
January 2, 2025
FLI1 and GATA1 govern <i>TLN1</i> transcription: new insights into FLI1-related platelet disorders
Elisa Gabinaud, Laurent Hannouche, Mathilde Veneziano-Broccia, et al.
Research and Practice in Thrombosis and Haemostasis
|
March 9, 2026
Platelet dense granule defect: experience in the French population
Delphine Borgel, Agathe Beauvais, Cécile Bally, et al.
Page
of 7