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Research and Practice in Thrombosis and Haemostasis
|
July 27, 2018
Defects of splicing in antithrombin deficiency
María E de la Morena-Barrio, Raquel López-Gálvez, Irene Martínez-Martínez, et al.
Archives of Pathology & Laboratory Medicine
|
September 12, 2024
Reduced Plasma Selenoprotein P Is Associated With Type I Antithrombin Deficiency and a Prothrombotic State
Adrianna Klajmon, Joanna Natorska, Javier Corral, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
January 30, 2007
Latent and polymeric antithrombin: clearance and potential thrombotic risk
Javier Corral, José Rivera, José A Guerrero, et al.
Urologia Internationalis
|
February 25, 2011
Long-term outcomes after robotic sacrocolpopexy in pelvic organ prolapse: prospective analysis
Jesús Moreno Sierra, Elena Ortiz Oshiro, Cristina Fernandez Pérez, et al.
Pharmacogenomics
|
June 24, 2014
Effect of VKORC1, CYP2C9 and CYP4F2 genetic variants in early outcomes during acenocoumarol treatment
Juan Jose Cerezo-Manchado, Vanessa Roldan, Mario Rosafalco, et al.
Thrombosis and Haemostasis
|
January 12, 2012
Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency
María Eugenia de la Morena-Barrio, Ana Isabel Antón, Irene Martínez-Martínez, et al.
British Journal of Haematology
|
April 25, 2009
Genotype-phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause
Constantino Martínez, Ana Isabel Antón, Javier Corral, et al.
Scientific Reports
|
March 18, 2017
Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy
Nuria Revilla, María Eugenia de la Morena-Barrio, Antonia Miñano, et al.
Glycobiology
|
August 22, 2021
Dissecting the transcriptional program of phosphomannomutase 2-deficient cells: Lymphoblastoide B cell lines as a valuable model for congenital disorders of glycosylation studies
Antonio Parrado, Gonzalo Rubio, Mercedes Serrano, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
December 31, 2019
Congenital antithrombin deficiency in patients with splanchnic vein thrombosis
Anna Baiges, María Eugenia de la Morena-Barrio, Fanny Turon, et al.
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of 20
Search research articles
Search
Showing results (131-140 of 197) with videos related to
Sort By:
Page
of 20
Research and Practice in Thrombosis and Haemostasis
|
July 27, 2018
Defects of splicing in antithrombin deficiency
María E de la Morena-Barrio, Raquel López-Gálvez, Irene Martínez-Martínez, et al.
Archives of Pathology & Laboratory Medicine
|
September 12, 2024
Reduced Plasma Selenoprotein P Is Associated With Type I Antithrombin Deficiency and a Prothrombotic State
Adrianna Klajmon, Joanna Natorska, Javier Corral, et al.
Experimental Biology and Medicine (Maywood, N.J.)
|
January 30, 2007
Latent and polymeric antithrombin: clearance and potential thrombotic risk
Javier Corral, José Rivera, José A Guerrero, et al.
Urologia Internationalis
|
February 25, 2011
Long-term outcomes after robotic sacrocolpopexy in pelvic organ prolapse: prospective analysis
Jesús Moreno Sierra, Elena Ortiz Oshiro, Cristina Fernandez Pérez, et al.
Pharmacogenomics
|
June 24, 2014
Effect of VKORC1, CYP2C9 and CYP4F2 genetic variants in early outcomes during acenocoumarol treatment
Juan Jose Cerezo-Manchado, Vanessa Roldan, Mario Rosafalco, et al.
Thrombosis and Haemostasis
|
January 12, 2012
Regulatory regions of SERPINC1 gene: identification of the first mutation associated with antithrombin deficiency
María Eugenia de la Morena-Barrio, Ana Isabel Antón, Irene Martínez-Martínez, et al.
British Journal of Haematology
|
April 25, 2009
Genotype-phenotype relationship for six common polymorphisms in genes affecting platelet function from 286 healthy subjects and 160 patients with mucocutaneous bleeding of unknown cause
Constantino Martínez, Ana Isabel Antón, Javier Corral, et al.
Scientific Reports
|
March 18, 2017
Transient desialylation in combination with a novel antithrombin deficiency causing a severe and recurrent thrombosis despite anticoagulation therapy
Nuria Revilla, María Eugenia de la Morena-Barrio, Antonia Miñano, et al.
Glycobiology
|
August 22, 2021
Dissecting the transcriptional program of phosphomannomutase 2-deficient cells: Lymphoblastoide B cell lines as a valuable model for congenital disorders of glycosylation studies
Antonio Parrado, Gonzalo Rubio, Mercedes Serrano, et al.
Liver International : Official Journal of the International Association for the Study of the Liver
|
December 31, 2019
Congenital antithrombin deficiency in patients with splanchnic vein thrombosis
Anna Baiges, María Eugenia de la Morena-Barrio, Fanny Turon, et al.
Page
of 20