José María
Bastida Bermejo
Profesor Asociado CC. Salud
José Ramón
González Porras
Profesor Asociado CC. Salud
Publicaciones en las que colabora con José Ramón González Porras (36)
2024
-
Platelet C3G: a key player in vesicle exocytosis, spreading and clot retraction
Cellular and Molecular Life Sciences, Vol. 81, Núm. 1
2023
-
Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation
International journal of molecular sciences, Vol. 24, Núm. 6
-
Key Genes of the Immune System and Predisposition to Acquired Hemophilia A: Evidence from a Spanish Cohort of 49 Patients Using Next-Generation Sequencing
International Journal of Molecular Sciences, Vol. 24, Núm. 22
-
Novel variants in GALE cause syndromic macrothrombocytopenia by disrupting glycosylation and thrombopoiesis
Blood, Vol. 141, Núm. 4, pp. 406-421
2022
-
A novel nonsense variant in TPM4 caused dominant macrothrombocytopenia, mild bleeding tendency and disrupted cytoskeleton remodeling
Journal of Thrombosis and Haemostasis, Vol. 20, Núm. 5, pp. 1248-1255
-
Functional Alterations Involved in Increased Bleeding in Hereditary Hemorrhagic Telangiectasia Mouse Models
Frontiers in Medicine, Vol. 9
-
Low molecular weight heparin is useful in adult COVID-19 inpatients. Experience during the first Spanish wave: observational study
Sao Paulo medical journal = Revista paulista de medicina, Vol. 140, Núm. 1, pp. 123-133
-
Novel Therapies to Address Unmet Needs in ITP
Pharmaceuticals, Vol. 15, Núm. 7
-
Retinal blood vessel calibre and vascular ageing in a general Spanish population: A EVA study
European Journal of Clinical Investigation, Vol. 52, Núm. 2
-
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
-
ABCG5 and ABCG8 gene variations associated with sitosterolemia and platelet dysfunction
Platelets, Vol. 32, Núm. 4, pp. 573-577
-
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
-
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
-
Inherited platelet disorders: An updated overview
International Journal of Molecular Sciences, Vol. 22, Núm. 9
-
Role of thrombopoietin receptor agonists in inherited thrombocytopenia
International Journal of Molecular Sciences, Vol. 22, Núm. 9
2020
-
Acquired haemophilia a in association with influenza a and urinary tract infection
European Journal of Case Reports in Internal Medicine, Vol. 7, Núm. 9
-
Reference values of arterial stiffness parameters and their association with cardiovascular risk factors in the Spanish population. The EVA Study
Revista Espanola de Cardiologia, Vol. 73, Núm. 1, pp. 43-52
-
Transcriptomic analysis of patients with immune thrombocytopenia treated with eltrombopag
Platelets, Vol. 31, Núm. 8, pp. 993-1000
2019
-
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
-
Molecular Diagnosis of Inherited Coagulation and Bleeding Disorders
Seminars in Thrombosis and Hemostasis, Vol. 45, Núm. 7, pp. 695-707