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Erythrocyte deformability and aggregation in homozygous sickle cell disease

Clinical hemorheology and microcirculation, 2014, Vol.58 (4), p.497-505

2014

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Erythrocyte aggregation in homozygous sickle cell disease

Clinical hemorheology and microcirculation, 2014, Vol.58 (3), p.475-477

2014

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Protocol for the study and treatment of primary immune thrombocytopenia: ITP-2018

Anales de Pediatría, 2019-08, Vol.91 (2), p.127.e1-127.e10

2019

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Protocolo de estudio y tratamiento de la trombocitopenia inmune primaria: PTI-2018

Anales de pediatría (Barcelona, Spain : 2003), 2019-08, Vol.91 (2), p.127.e1-127.e10

2019

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A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain

Blood, 2005-03, Vol.105 (5), p.1946-1949

2005

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Severe and moderate hemophilia A: identification of 38 new genetic alterations

Haematologica (Roma), 2008-07, Vol.93 (7), p.1091-1094

2008

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Trasplante de progenitores hematopoyéticos con intensidad reducida en enfermedades genéticas. Experiencia del grupo GETMON (Grupo Español de Trasplante de Médula Ósea en Niños)

Anales de pediatría (Barcelona, Spain : 2003), 2018-04, Vol.88 (4), p.196-203

2018

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Tapering of the thrombopoietin receptor agonist in paediatric patients with chronic immune thrombocytopenia: Is it possible?

British journal of clinical pharmacology, 2022-09, Vol.88 (9), p.4220-4223

2022

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Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow Transplantation in Children

Anales de Pediatría, 2018-04, Vol.88 (4), p.196-203

2018

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C0475: Cerebral Sinus Venous Thrombosis in Children: An Emergent Disease

Thrombosis research, 2014-05, Vol.133, p.S22-S23

2014

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Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype

American journal of human genetics, 2007-05, Vol.80 (5), p.895-910

2007

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Detectable clonal mosaicism in blood as a biomarker of cancer risk in Fanconi anemia

Blood advances, 2017-01, Vol.1 (5), p.319-329

2017

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C0532: Novel Mutations in the Gamma Carboxylase Gene Causing VKCFD1

Thrombosis research, 2014-05, Vol.133, p.S23-S23

2014

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Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact

Journal of medical genetics, 2011-04, Vol.48 (4), p.242-250

2011

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Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow Transplantation in Children

Anales de Pediatría, 2018-04, Vol.88 (4), p.196-203

2018

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C0529: Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency: Report of a New Case

Thrombosis research, 2014-05, Vol.133, p.S92-S92

2014

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Protocol for the study and treatment of primary immune thrombocytopenia: ITP-2018

Anales de Pediatría, 2019-08, Vol.91 (2), p.127.e1-127.e10

2019

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Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow Transplantation in Children

Anales de Pediatría, 2018-04, Vol.88 (4), p.196-203

2018

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Protocol for the study and treatment of primary immune thrombocytopenia: PTI-2018

Anales de Pediatría, 2019-08, Vol.91 (2), p.127.e1-127.e10

2019

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Protocol for the study and treatment of primary immune thrombocytopenia: PTI-2018

Anales de Pediatría, 2019-08, Vol.91 (2), p.127.e1

2019

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C0240 Safety and efficacy of anticoagulation in cerebral sinus thrombosis in children: A single center experience

Thrombosis research, 2012-10, Vol.130, p.S129-S129

2012

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C0195 The presence of the TXA2 receptor in lipid rafts of platelets is necessary for platelet activation by TXA2

Thrombosis research, 2012-10, Vol.130, p.S103-S103

2012

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The Interaction Between Collagen-Activated Platelets and Erythrocytes Selectively Increases the Release of Subsets of Platelet α-Granules Containing Pro-Angiogenic Substances

Blood, 2014-12, Vol.124 (21), p.4171-4171

2014

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Erythrocyte deformability and aggregation in homozygous sickle cell disease

Erythrocyte aggregation in homozygous sickle cell disease

Protocol for the study and treatment of primary immune thrombocytopenia: ITP-2018

Protocolo de estudio y tratamiento de la trombocitopenia inmune primaria: PTI-2018

A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain

Severe and moderate hemophilia A: identification of 38 new genetic alterations

Trasplante de progenitores hematopoyéticos con intensidad reducida en enfermedades genéticas. Experiencia del grupo GETMON (Grupo Español de Trasplante de Médula Ósea en Niños)

Tapering of the thrombopoietin receptor agonist in paediatric patients with chronic immune thrombocytopenia: Is it possible?

Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow Transplantation in Children

C0475: Cerebral Sinus Venous Thrombosis in Children: An Emergent Disease

Hypomorphic Mutations in the Gene Encoding a Key Fanconi Anemia Protein, FANCD2, Sustain a Significant Group of FA-D2 Patients with Severe Phenotype

Detectable clonal mosaicism in blood as a biomarker of cancer risk in Fanconi anemia

Origin, functional role, and clinical impact of Fanconi anemia FANCA mutations

C0532: Novel Mutations in the Gamma Carboxylase Gene Causing VKCFD1

Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact

Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow Transplantation in Children

C0529: Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency: Report of a New Case

Protocol for the study and treatment of primary immune thrombocytopenia: ITP-2018

Reduced-intensity conditioning haematopoietic stem cell transplantation in genetic diseases: Experience of the Spanish Working Group for Bone Marrow Transplantation in Children

A comprehensive strategy for the subtyping of patients with Fanconi anaemia: conclusions from the Spanish Fanconi Anemia Research Network

Protocol for the study and treatment of primary immune thrombocytopenia: PTI-2018

Protocol for the study and treatment of primary immune thrombocytopenia: PTI-2018

C0240 Safety and efficacy of anticoagulation in cerebral sinus thrombosis in children: A single center experience

C0195 The presence of the TXA2 receptor in lipid rafts of platelets is necessary for platelet activation by TXA2

The Interaction Between Collagen-Activated Platelets and Erythrocytes Selectively Increases the Release of Subsets of Platelet α-Granules Containing Pro-Angiogenic Substances

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