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Common Genetic Variants in ABO and CLEC4M Modulate the Pharmacokinetics of Recombinant FVIII in Severe Hemophilia A Patients

Thrombosis and haemostasis, 2020-10, Vol.120 (10), p.1395-1406

2020

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Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene

Thrombosis and haemostasis, 2009-03, Vol.101 (3), p.570-576

2009

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Integration of molecular and clinical data of 40 unrelated von Willebrand Disease families in a Spanish locus-specific mutation database: first release including 58 mutations

Haematologica (Roma), 2010-11, Vol.95 (11), p.1982-1984

2010

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Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations

Thrombosis and haemostasis, 2001-04, Vol.85 (4), p.580-583

2001

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A versatile strategy for preimplantation genetic diagnosis of haemophilia A based on F8-gene sequencing

Thrombosis and haemostasis, 2006-12, Vol.96 (6), p.839-845

2006

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The evolving role and future relevance of plasma-derived therapies in the management of bleeding disorders

Thrombosis and haemostasis, 2016, Vol.116 (S 01), p.S1

2016

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Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients

Haematologica (Roma), 2017-12, Vol.102 (12), p.2005-2014

2017

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Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA

Haematologica (Roma), 2019-03, Vol.104 (3), p.587-598

2019

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Von Willebrand gene tracking by single-tube automated fluorescent analysis of four short tandem repeat polymorphisms

Thrombosis and haemostasis, 2005-05, Vol.93 (5), p.976-981

2005

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Alterations of ADAMTS-13 Activity as a Common Indicator of the Endothelial Dysfunction Developing in Different Thrombotic Microangiopathies

Blood, 2006-11, Vol.108 (11), p.4091-4091

2006

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Diátesis hemorrágica en un varón de 67 años de edad con dolor e impotencia funcional de la extremidad inferior izquierda

Medicina clínica, 2002, Vol.118 (3), p.111-116

2002

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Implications of gene sequencing in the direct diagnosis of hemophilia by PCR-RFLP

Haematologica (Roma), 2002-01, Vol.87 (1), p.109

2002

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Recombinant activated factor VII in uncontrolled hemorrhage

Medicina clínica, 2005-02, Vol.124 (4), p.156

2005

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Factor VII activado recombinante en la hemorragia masiva

Medicina clínica, 2005-02, Vol.124 (4), p.156-156

2005

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Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis : identification of two novel mutations

British journal of haematology, 2000-11, Vol.111 (2), p.549-551

2000

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Factor IX gene sequencing by a simple and sensitive 15‐hour procedure for haemophilia B diagnosis: identification of two novel mutations

British journal of haematology, 2000-11, Vol.111 (2), p.549-551

2000

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Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. SHORT REPORT

British journal of haematology, 2000-11, Vol.111 (2), p.549-551

2000

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Factor IX gene sequencing by a simple and sensitive 15‐hour procedure for haemophilia B diagnosis: identification of two novel mutations: SHORT REPORT

British journal of haematology, 2000-11, Vol.111 (2), p.549-551

2000

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Hemorrhagic diathesis in a 67-year-old male with pain and limited mobility of the lower left limb

Medicina clinica, 2002-02, Vol.118 (3), p.111-116

2002

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A Novel Mutation (2409delT) in Exon 14 of the Factor VIII Gene Causes Severe Haemophilia A

Human heredity, 2000-07, Vol.50 (4), p.266-267

2000

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Absence of mutations in the granulocyte colony-stimulating factor (G-CSF) receptor gene in patients with myelodysplastic syndrome/acute myeloblastic leukaemia occurring after treatment of aplastic anaemia with G-CSF

British journal of haematology, 2000-11, Vol.111 (2), p.656-658

2000

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Hepatitis G virus infection markers (RNA and anti-E2 antibodies) in a multicenter cohort of hemophiliacs

Haematologica (Roma), 1999-10, Vol.84 (10), p.930

1999

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Seudotumor hemofílico pelviano

Cirugia Española, 2007-02, Vol.81 (2), p.102-104

2007

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Hemophilic pelvic pseudotumor

Cirugia Española, 2007-02, Vol.81 (2), p.102-104

2007

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Transient factor VIII inhibitor and treatment with monoclonal-antibody-purified factor VIII

The Lancet (British edition), 1991-05, Vol.337 (8751), p.1222-1222

1991

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Common Genetic Variants in ABO and CLEC4M Modulate the Pharmacokinetics of Recombinant FVIII in Severe Hemophilia A Patients

Rapid molecular diagnosis of von Willebrand disease by direct sequencing. Detection of 12 novel putative mutations in VWF gene

Integration of molecular and clinical data of 40 unrelated von Willebrand Disease families in a Spanish locus-specific mutation database: first release including 58 mutations

Rapid hemophilia A molecular diagnosis by a simple DNA sequencing procedure: identification of 14 novel mutations

A versatile strategy for preimplantation genetic diagnosis of haemophilia A based on F8-gene sequencing

The evolving role and future relevance of plasma-derived therapies in the management of bleeding disorders

Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): comprehensive genetic analysis by next-generation sequencing of 480 patients

Unraveling the effect of silent, intronic and missense mutations on VWF splicing: contribution of next generation sequencing in the study of mRNA

Von Willebrand gene tracking by single-tube automated fluorescent analysis of four short tandem repeat polymorphisms

Alterations of ADAMTS-13 Activity as a Common Indicator of the Endothelial Dysfunction Developing in Different Thrombotic Microangiopathies

Diátesis hemorrágica en un varón de 67 años de edad con dolor e impotencia funcional de la extremidad inferior izquierda

Implications of gene sequencing in the direct diagnosis of hemophilia by PCR-RFLP

Recombinant activated factor VII in uncontrolled hemorrhage

Factor VII activado recombinante en la hemorragia masiva

Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis : identification of two novel mutations

Factor IX gene sequencing by a simple and sensitive 15‐hour procedure for haemophilia B diagnosis: identification of two novel mutations

Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. SHORT REPORT

Factor IX gene sequencing by a simple and sensitive 15‐hour procedure for haemophilia B diagnosis: identification of two novel mutations: SHORT REPORT

Hemorrhagic diathesis in a 67-year-old male with pain and limited mobility of the lower left limb

A Novel Mutation (2409delT) in Exon 14 of the Factor VIII Gene Causes Severe Haemophilia A

Absence of mutations in the granulocyte colony-stimulating factor (G-CSF) receptor gene in patients with myelodysplastic syndrome/acute myeloblastic leukaemia occurring after treatment of aplastic anaemia with G-CSF

Hepatitis G virus infection markers (RNA and anti-E2 antibodies) in a multicenter cohort of hemophiliacs

Seudotumor hemofílico pelviano

Hemophilic pelvic pseudotumor

Transient factor VIII inhibitor and treatment with monoclonal-antibody-purified factor VIII

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