Publikationen, an denen er mitarbeitet Pablo Morales Pérez (57)

2024

  1. Enrichment of Immune Dysregulation Disorders in Adult Patients with Human Inborn Errors of Immunity

    Journal of Clinical Immunology, Vol. 44, Núm. 3

2023

  1. Novel Germline TET2 Mutations in Two Unrelated Patients with Autoimmune Lymphoproliferative Syndrome-Like Phenotype and Hematologic Malignancy

    Journal of Clinical Immunology, Vol. 43, Núm. 1, pp. 165-180

2022

  1. An Early Th1 Response Is a Key Factor for a Favorable COVID-19 Evolution

    Biomedicines, Vol. 10, Núm. 2

  2. Overcoming CAR-Mediated CD19 Downmodulation and Leukemia Relapse with T Lymphocytes Secreting Anti-CD19 T-cell Engagers

    Cancer immunology research, Vol. 10, Núm. 4, pp. 498-511

2020

  1. Perforin gene variant A91V in young patients with severe COVID-19

    Haematologica

2016

  1. Early renal graft function deterioration in recipients with preformed anti-MICA antibodies: Partial contribution of complement-dependent cytotoxicity

    Nephrology Dialysis Transplantation, Vol. 31, Núm. 1, pp. 150-160

  2. Study of β2–Glycoprotein I Polymorphisms in Patients With Chronic Renal Failure as a Predisposing Factor for the Development of Anti–β2–Glycoprotein I Auto-Antibodies

    Transplantation Proceedings, Vol. 48, Núm. 9, pp. 2876-2879

2014

  1. Comparison of several functional methods to evaluate the immune response on stable kidney transplant patients

    Journal of Immunological Methods, Vol. 403, Núm. 1-2, pp. 62-65

2013

  1. Harmful effect of preformed anti-MICA antibodies on renal allograft evolution in early posttransplantation period

    Transplantation, Vol. 96, Núm. 1, pp. 70-78

2012

  1. Clinical and genetic characteristics in a series of haemophagocytic lymphohistiocytosis patients without perforin defects

    Inmunologia, Vol. 31, Núm. 1, pp. 13-20

  2. Complement C3 genotyping of slow and fast variants by real time PCR-high resolution melting

    European Journal of Inflammation, Vol. 10, Núm. 3, pp. 329-334

2009

  1. An In Vitro Model of Cell Transplantation for Evaluation of Cell Engraftment Enhancers

    Transplantation Proceedings, Vol. 41, Núm. 6, pp. 2487-2490

  2. Frequency and Influence of Hemochromatosis Gene Mutations in Kidney Transplant Recipients With or Without Hepatitis C Virus Infection

    Transplantation Proceedings, Vol. 41, Núm. 6, pp. 2422-2424

2008

  1. Preformed antibodies detected by cytotoxic assay or multibead array decrease liver allograft survival: Role of human leukocyte antigen compatibility

    Liver Transplantation, Vol. 14, Núm. 4, pp. 554-562

2006

  1. A homozygous Fas ligand gene mutation in a patient causes a new type of autoimmune lymphoproliferative syndrome

    Blood, Vol. 108, Núm. 4, pp. 1306-1312

  2. A novel RMRP mutation in a Spanish patient with cartilage-hair hypoplasia

    Immunobiology, Vol. 211, Núm. 9, pp. 753-757

  3. The A247E mutation in human FASL gene and the classification of autoimmune lymphoproliferative syndrome (ALPS) [6]

    Blood

2005

  1. Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda

    Journal of Gastroenterology and Hepatology (Australia), Vol. 20, Núm. 3, pp. 456-462

  2. MHC-F DNA sequences in bonobo, gorilla and orangutan

    Tissue Antigens, Vol. 66, Núm. 4, pp. 277-283

  3. Rapid molecular diagnosis of ataxia-telangiectasia by optimised RT-PCR and direct sequencing analysis

    Immunobiology, Vol. 210, Núm. 5, pp. 279-282