José María
Bastida Bermejo
Profesor Asociado CC. Salud
Hospital Universitario de Salamanca
Salamanca, EspañaPublicaciones en colaboración con investigadores/as de Hospital Universitario de Salamanca (40)
2024
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Platelet C3G: a key player in vesicle exocytosis, spreading and clot retraction
Cellular and Molecular Life Sciences, Vol. 81, Núm. 1
2023
2022
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Novel Therapies to Address Unmet Needs in ITP
Pharmaceuticals, Vol. 15, Núm. 7
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Thrombocytopenia and Therapeutic Strategies after Allogeneic Hematopoietic Stem Cell Transplantation
Journal of Clinical Medicine, Vol. 11, Núm. 5
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Vascular target organ damage in patients with Philadelphia negative myeloproliferative syndrome: A propensity score analysis
Medicina Clinica, Vol. 158, Núm. 11, pp. 503-508
2021
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ABCG5 and ABCG8 gene variations associated with sitosterolemia and platelet dysfunction
Platelets, Vol. 32, Núm. 4, pp. 573-577
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PTGS1 gene variations associated with bleeding and platelet dysfunction
Platelets, Vol. 32, Núm. 5, pp. 710-716
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A novel genetic variant in PTGS1 affects N-glycosylation of cyclooxygenase-1 causing a dominant-negative effect on platelet function and bleeding diathesis
American Journal of Hematology
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Biological significance of monoallelic and biallelic BIRC3 loss in del(11q) chronic lymphocytic leukemia progression
Blood Cancer Journal, Vol. 11, Núm. 7
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Characterization of the platelet phenotype caused by a germline RUNX1 Variant in a CRISPR/Cas9-generated murine model
Thrombosis and Haemostasis, Vol. 121, Núm. 9, pp. 1193-1205
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Expanding the genetic spectrum of TUBB1-related thrombocytopenia
Blood Advances, Vol. 5, Núm. 24, pp. 5453-5467
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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
Journal of Thrombosis and Haemostasis, Vol. 19, Núm. 10, pp. 2612-2617
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Management of acquired hemophilia A: results from the Spanish registry
Blood Advances, Vol. 5, Núm. 19, pp. 3821-3829
2020
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Acquired haemophilia a in association with influenza a and urinary tract infection
European Journal of Case Reports in Internal Medicine, Vol. 7, Núm. 9
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CRISPR/Cas9-generated models uncover therapeutic vulnerabilities of del(11q) CLL cells to dual BCR and PARP inhibition
Leukemia, Vol. 34, Núm. 6, pp. 1599-1612
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Transcriptomic analysis of patients with immune thrombocytopenia treated with eltrombopag
Platelets, Vol. 31, Núm. 8, pp. 993-1000
2019
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Defects in memory B-cell and plasma cell subsets expressing different immunoglobulin-subclasses in patients with CVID and immunoglobulin subclass deficiencies
Journal of Allergy and Clinical Immunology, Vol. 144, Núm. 3, pp. 809-824
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GENYOi005-A: An induced pluripotent stem cells (iPSCs) line generated from a patient with Familial Platelet Disorder with associated Myeloid Malignancy (FPDMM) carrying a p.Thr196Ala variant
Stem Cell Research, Vol. 41
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Hidden myelodysplastic syndrome (MDS): A prospective study to confirm or exclude MDS in patients with anemia of uncertain etiology
International Journal of Laboratory Hematology, Vol. 41, Núm. 1, pp. 109-117
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Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing
Annals of Medicine, Vol. 51, Núm. 2, pp. 141-148