Publicaciones en colaboración con investigadores/as de University of Münster (14)

2024

  1. Characterization of the molecular composition and in vitro regenerative capacity of platelet-based bioproducts and related subfractions

    Acta Biomaterialia, Vol. 177, pp. 132-147

  2. Predicting survival in patients with ‘non-high-risk’ acute variceal bleeding receiving β-blockers+ligation to prevent re-bleeding

    Journal of Hepatology, Vol. 80, Núm. 1, pp. 73-81

2022

  1. Dissecting platelet proteomics to understand the pathophysiology of immune thrombocytopenia: studies in mouse models

    Blood Advances, Vol. 6, Núm. 11, pp. 3529-3534

  2. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Nature, Vol. 604, Núm. 7906, pp. 502-508

  3. Platelet number and function alterations in preclinical models of sterile inflammation and sepsis patients: implications in the pathophysiology and treatment of inflammation

    Transfusion and Apheresis Science, Vol. 61, Núm. 2

2021

  1. A European observational study to evaluate the safety and the effectiveness of safinamide in routine clinical practice: The SynapSES trial

    Journal of Parkinson's Disease, Vol. 11, Núm. 1, pp. 187-198

  2. Impact on carer burden when stable patients with schizophrenia transitioned from 1-monthly to 3-monthly paliperidone palmitate

    Comprehensive Psychiatry, Vol. 107

2014

  1. Birthweight and the risk of atopic diseases: The ISAAC Phase III study

    Pediatric Allergy and Immunology, Vol. 25, Núm. 3, pp. 264-270

  2. Evidence of a third ADPKD locus is not supported by re-analysis of designated PKD3 families

    Kidney International

2010

  1. Genetic variation of DKK3 may modify renal disease severity in ADPKD

    Journal of the American Society of Nephrology, Vol. 21, Núm. 9, pp. 1510-1520

2003

  1. Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney disease

    Journal of the American Society of Nephrology, Vol. 14, Núm. 5, pp. 1164-1174

2000

  1. Location of mutations within the PKD2 gene influences clinical outcome

    Kidney International

1999

  1. Comparison of phonotypes of polycystic kidney disease types 1 and 2

    Lancet, Vol. 353, Núm. 9147, pp. 103-107

1997

  1. A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2)

    American Journal of Human Genetics, Vol. 61, Núm. 3, pp. 547-555