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Martine Alhenc-Gelas

Showing results (1-10 of 55) with videos related to

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Annales De Biologie Clinique|April 17, 2014
[Stability of coagulation parameters: review of available data]Laetitia Mauge, Martine Alhenc-Gelas
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 30, 2013
Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation: a case reportMagdalena Szymańska, Martine Alhenc-Gelas, Anetta Undas
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 29, 2013
Antithrombin Rybnik: a new point mutation (nt 683 G>T) associated with type I antithrombin deficiency in a patient with venous thromboembolism and recurrent superficial venous thrombosisMagdalena Szymańska, Martine Alhenc-Gelas, Anetta Undas
Thrombosis Research|March 12, 2013
First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosisEwa Wypasek, Martine Alhenc-Gelas, Anetta Undas
Journal of Genetics|January 12, 2018
Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature reviewEwa Wypasek, Marek Karpinski, Martine Alhenc-Gelas, et al.
Polskie Archiwum Medycyny Wewnetrznej|February 6, 2014
Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolismEwa Wypasek, Daniel P Potaczek, Martine Alhenc-Gelas, et al.
Thrombosis Research|February 11, 2014
PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapyEwa Wypasek, Daniel P Potaczek, Martine Alhenc-Gelas, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 25, 2013
Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosisEwa Wypasek, Daniel P Potaczek, Martine Alhenc-Gelas, et al.
Journal of Pediatric Hematology/Oncology|January 7, 2004
Late onset of clinical symptoms and recurrent ecchymotic skin lesions in a 12-year-old girl with a severe double heterozygous protein C deficiencyMichèle Loop, Alina Ferster, Francis Corazza, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 2, 2014
Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiencyMarek Cieśla, Ewa Wypasek, Javier Corral, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Annales De Biologie Clinique|April 17, 2014
[Stability of coagulation parameters: review of available data]Laetitia Mauge, Martine Alhenc-Gelas
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|January 30, 2013
Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation: a case reportMagdalena Szymańska, Martine Alhenc-Gelas, Anetta Undas
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 29, 2013
Antithrombin Rybnik: a new point mutation (nt 683 G>T) associated with type I antithrombin deficiency in a patient with venous thromboembolism and recurrent superficial venous thrombosisMagdalena Szymańska, Martine Alhenc-Gelas, Anetta Undas
Thrombosis Research|March 12, 2013
First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosisEwa Wypasek, Martine Alhenc-Gelas, Anetta Undas
Journal of Genetics|January 12, 2018
Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature reviewEwa Wypasek, Marek Karpinski, Martine Alhenc-Gelas, et al.
Polskie Archiwum Medycyny Wewnetrznej|February 6, 2014
Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolismEwa Wypasek, Daniel P Potaczek, Martine Alhenc-Gelas, et al.
Thrombosis Research|February 11, 2014
PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapyEwa Wypasek, Daniel P Potaczek, Martine Alhenc-Gelas, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|December 25, 2013
Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosisEwa Wypasek, Daniel P Potaczek, Martine Alhenc-Gelas, et al.
Journal of Pediatric Hematology/Oncology|January 7, 2004
Late onset of clinical symptoms and recurrent ecchymotic skin lesions in a 12-year-old girl with a severe double heterozygous protein C deficiencyMichèle Loop, Alina Ferster, Francis Corazza, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 2, 2014
Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiencyMarek Cieśla, Ewa Wypasek, Javier Corral, et al.
Pageof 6