Search research articles
Contact Us
Filters
Showing results (1-10 of 14) with videos related to
Page
of 2
Sort By:
Biomolecules
|
November 27, 2025
Molecular Pathogenesis of Inherited Platelet Dysfunction
Agustín Rodríguez-Alén, Antonio Moscardó, José M Bastida, et al.
Blood Reviews
|
May 30, 2026
Platelet biology and etiopathogenesis of congenital platelet disorders
Ana C Glembotsky, Nora V Butta, José M Bastida, et al.
Biomolecules
|
June 26, 2025
Diagnosis of Inherited Platelet Disorders: Clinical Evaluation and Functional and Molecular Assays
Ana Sánchez-Fuentes, Juliana Pérez-Botero, José M Bastida, et al.
Cells
|
October 27, 2022
A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger
José M Bastida, Stefano Malvestiti, Doris Boeckelmann, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
Karyn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
Medicina Clinica
|
August 17, 2021
Vascular target organ damage in patients with Philadelphia negative myeloproliferative syndrome: A propensity score analysis
Carmen Patino-Alonso, Marta Gómez-Sánchez, Jesús M Hernández-Rivas, et al.
Molecular Oncology
|
March 25, 2025
Tonic signaling of the B-cell antigen-specific receptor is a common functional hallmark in chronic lymphocytic leukemia cell phosphoproteomes at early disease stages
Paula Díez, Pablo Juanes-Velasco, Marina L García-Vaquero, et al.
Plos One
|
March 2, 2017
HLA specificities are associated with prognosis in IGHV-mutated CLL-like high-count monoclonal B cell lymphocytosis
María García-Álvarez, Miguel Alcoceba, Miriam López-Parra, et al.
Blood Advances
|
September 13, 2021
Expanding the genetic spectrum of TUBB1-related thrombocytopenia
Verónica Palma-Barqueros, Loredana Bury, Shinji Kunishima, et al.
Haematologica
|
October 7, 2017
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
José M Bastida, María L Lozano, Rocío Benito, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Biomolecules
|
November 27, 2025
Molecular Pathogenesis of Inherited Platelet Dysfunction
Agustín Rodríguez-Alén, Antonio Moscardó, José M Bastida, et al.
Blood Reviews
|
May 30, 2026
Platelet biology and etiopathogenesis of congenital platelet disorders
Ana C Glembotsky, Nora V Butta, José M Bastida, et al.
Biomolecules
|
June 26, 2025
Diagnosis of Inherited Platelet Disorders: Clinical Evaluation and Functional and Molecular Assays
Ana Sánchez-Fuentes, Juliana Pérez-Botero, José M Bastida, et al.
Cells
|
October 27, 2022
A Novel GATA1 Variant in the C-Terminal Zinc Finger Compared with the Platelet Phenotype of Patients with A Likely Pathogenic Variant in the N-Terminal Zinc Finger
José M Bastida, Stefano Malvestiti, Doris Boeckelmann, et al.
Journal of Thrombosis and Haemostasis : JTH
|
August 6, 2021
GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis
Karyn Megy, Kate Downes, Marie-Christine Morel-Kopp, et al.
Medicina Clinica
|
August 17, 2021
Vascular target organ damage in patients with Philadelphia negative myeloproliferative syndrome: A propensity score analysis
Carmen Patino-Alonso, Marta Gómez-Sánchez, Jesús M Hernández-Rivas, et al.
Molecular Oncology
|
March 25, 2025
Tonic signaling of the B-cell antigen-specific receptor is a common functional hallmark in chronic lymphocytic leukemia cell phosphoproteomes at early disease stages
Paula Díez, Pablo Juanes-Velasco, Marina L García-Vaquero, et al.
Plos One
|
March 2, 2017
HLA specificities are associated with prognosis in IGHV-mutated CLL-like high-count monoclonal B cell lymphocytosis
María García-Álvarez, Miguel Alcoceba, Miriam López-Parra, et al.
Blood Advances
|
September 13, 2021
Expanding the genetic spectrum of TUBB1-related thrombocytopenia
Verónica Palma-Barqueros, Loredana Bury, Shinji Kunishima, et al.
Haematologica
|
October 7, 2017
Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders
José M Bastida, María L Lozano, Rocío Benito, et al.
Page
of 2