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Keith Gomez

Showing results (41-50 of 58) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|December 17, 2025
International Practices in Managing Preconception, Pregnancy and Childbirth in Women With Glanzmann Thrombasthenia: A Survey From the European Association of Haemophilia and Allied Disorders (EAHAD)Karlijn H G Rutten, Roger E G Schutgens, Roseline d'Oiron, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|November 26, 2013
Global Emerging HEmophilia Panel (GEHEP): A Multinational Collaboration for Advancing Hemophilia Research and TreatmentPaula James, Raj Kasthuri, Rebecca Kruse-Jarres, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 3, 2021
European principles of care for women and girls with inherited bleeding disordersKarin van Galen, Michelle Lavin, Naja Skouw-Rasmussen, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 22, 2021
Challenges of antithrombotic therapy in the management of cardiovascular disease in patients with inherited bleeding disorders: A single-centre experienceOliver C Cohen, Michele Bertelli, Gavin Manmathan, et al.
Journal of Thrombosis and Haemostasis : JTH|August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and HemostasisKaryn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
Journal of Thrombosis and Haemostasis : JTH|March 22, 2024
Standardization of definition and management for bleeding disorder of unknown cause: communication from the SSC of the ISTHRoss I Baker, Philip Choi, Nicola Curry, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Blood|June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopeniaClaire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.
Blood|August 30, 2023
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participantsLuca Stefanucci, Janine Collins, Matthew C Sims, et al.
Human Mutation|September 29, 2019
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variantsLoredana Bury, Karyn Megy, Jonathan C Stephens, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 17, 2025
International Practices in Managing Preconception, Pregnancy and Childbirth in Women With Glanzmann Thrombasthenia: A Survey From the European Association of Haemophilia and Allied Disorders (EAHAD)Karlijn H G Rutten, Roger E G Schutgens, Roseline d'Oiron, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|November 26, 2013
Global Emerging HEmophilia Panel (GEHEP): A Multinational Collaboration for Advancing Hemophilia Research and TreatmentPaula James, Raj Kasthuri, Rebecca Kruse-Jarres, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 3, 2021
European principles of care for women and girls with inherited bleeding disordersKarin van Galen, Michelle Lavin, Naja Skouw-Rasmussen, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 22, 2021
Challenges of antithrombotic therapy in the management of cardiovascular disease in patients with inherited bleeding disorders: A single-centre experienceOliver C Cohen, Michele Bertelli, Gavin Manmathan, et al.
Journal of Thrombosis and Haemostasis : JTH|August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and HemostasisKaryn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
Journal of Thrombosis and Haemostasis : JTH|March 22, 2024
Standardization of definition and management for bleeding disorder of unknown cause: communication from the SSC of the ISTHRoss I Baker, Philip Choi, Nicola Curry, et al.
Haematologica|November 24, 2018
Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopeniaTadbir K Bariana, Veerle Labarque, Jessica Heremans, et al.
Blood|June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopeniaClaire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.
Blood|August 30, 2023
The effects of pathogenic and likely pathogenic variants for inherited hemostasis disorders in 140 214 UK Biobank participantsLuca Stefanucci, Janine Collins, Matthew C Sims, et al.
Human Mutation|September 29, 2019
Next-generation sequencing for the diagnosis of MYH9-RD: Predicting pathogenic variantsLoredana Bury, Karyn Megy, Jonathan C Stephens, et al.
Pageof 6