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Keith Gomez

Showing results (31-40 of 58) with videos related to

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Haemophilia : the Official Journal of the World Federation of Hemophilia|October 30, 2023
Indirect treatment comparisons of the gene therapy etranacogene dezaparvovec versus extended half-life factor IX therapies for severe or moderately severe haemophilia BRobert Klamroth, Ashley Bonner, Keith Gomez, et al.
Thrombosis and Haemostasis|August 5, 2009
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiencyRebecca E Saunders, Nuha Shiltagh, Keith Gomez, et al.
Journal of Thrombosis and Haemostasis : JTH|October 20, 2020
Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTHKate Downes, Pascal Borry, Katrin Ericson, et al.
BMJ Open|March 12, 2020
Cohort profile: social well-being and determinants of health study (SWADES), Kerala, IndiaSaju M D, Lovakanth Nukala, Rameela Shekhar, et al.
British Journal of Haematology|June 17, 2004
Two novel mutations in severe factor VII deficiencyKeith Gomez, Michael A Laffan, Geoffrey Kemball-Cook, et al.
Research and Practice in Thrombosis and Haemostasis|February 29, 2020
Impaired platelet-dependent thrombin generation associated with thrombocytopenia is improved by prothrombin complex concentrates in vitroPratima Chowdary, Colleen Hamid, David Slatter, et al.
Human Mutation|April 26, 2020
The EAHAD blood coagulation factor VII variant databaseMuriel Giansily-Blaizot, Pavithra M Rallapalli, Stephen J Perkins, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2020
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchersJohn H McVey, Pavithra M Rallapalli, Geoffrey Kemball-Cook, et al.
Blood|August 19, 2009
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factorAnne F Riddell, Keith Gomez, Carolyn M Millar, et al.
Research and Practice in Thrombosis and Haemostasis|June 8, 2026
Menstrual outcomes are frequently overlooked in von Willebrand disease trialsMeaghan O'Donnell, Claire Kelly, Rezan Abdul Kadir, et al.
Pageof 6

Showing results (31-40 of 58) with videos related to

Sort By:
Pageof 6
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 30, 2023
Indirect treatment comparisons of the gene therapy etranacogene dezaparvovec versus extended half-life factor IX therapies for severe or moderately severe haemophilia BRobert Klamroth, Ashley Bonner, Keith Gomez, et al.
Thrombosis and Haemostasis|August 5, 2009
Structural analysis of eight novel and 112 previously reported missense mutations in the interactive FXI mutation database reveals new insight on FXI deficiencyRebecca E Saunders, Nuha Shiltagh, Keith Gomez, et al.
Journal of Thrombosis and Haemostasis : JTH|October 20, 2020
Clinical management, ethics and informed consent related to multi-gene panel-based high throughput sequencing testing for platelet disorders: Communication from the SSC of the ISTHKate Downes, Pascal Borry, Katrin Ericson, et al.
BMJ Open|March 12, 2020
Cohort profile: social well-being and determinants of health study (SWADES), Kerala, IndiaSaju M D, Lovakanth Nukala, Rameela Shekhar, et al.
British Journal of Haematology|June 17, 2004
Two novel mutations in severe factor VII deficiencyKeith Gomez, Michael A Laffan, Geoffrey Kemball-Cook, et al.
Research and Practice in Thrombosis and Haemostasis|February 29, 2020
Impaired platelet-dependent thrombin generation associated with thrombocytopenia is improved by prothrombin complex concentrates in vitroPratima Chowdary, Colleen Hamid, David Slatter, et al.
Human Mutation|April 26, 2020
The EAHAD blood coagulation factor VII variant databaseMuriel Giansily-Blaizot, Pavithra M Rallapalli, Stephen J Perkins, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 14, 2020
The European Association for Haemophilia and Allied Disorders (EAHAD) Coagulation Factor Variant Databases: Important resources for haemostasis clinicians and researchersJohn H McVey, Pavithra M Rallapalli, Geoffrey Kemball-Cook, et al.
Blood|August 19, 2009
Characterization of W1745C and S1783A: 2 novel mutations causing defective collagen binding in the A3 domain of von Willebrand factorAnne F Riddell, Keith Gomez, Carolyn M Millar, et al.
Research and Practice in Thrombosis and Haemostasis|June 8, 2026
Menstrual outcomes are frequently overlooked in von Willebrand disease trialsMeaghan O'Donnell, Claire Kelly, Rezan Abdul Kadir, et al.
Pageof 6