Hospital Universitario Pío del Río Hortega -ko ikertzaileekin lankidetzan egindako argitalpenak (7)

2019

  1. Novel presenilin 1 mutation (p.Thr-Pro116-117Ser-Thr) in a Spanish family with early-onset Alzheimer's disease

    Neurobiology of Aging, Vol. 84, pp. 238.e19-238.e24

2018

  1. Polymorphisms in receptors involved in opsonic and nonopsonic phagocytosis, and correlation with risk of infection in oncohematology patients

    Infection and Immunity, Vol. 86, Núm. 12

2010

  1. PRPH2 (Peripherin/RDS) mutations associated with different macular dystrophies in a Spanish population: A new mutation

    European Journal of Ophthalmology, Vol. 20, Núm. 4, pp. 724-732

2008

  1. ALOX5 promoter genotype and response to montelukast in moderate persistent asthma

    Respiratory Medicine, Vol. 102, Núm. 6, pp. 857-861

2006

  1. Farmacogenética en el tratamiento del asma

    Anales de Pediatria

  2. Tachyphylaxis to β2-agonists in Spanish asthmatic patients could be modulated by β2-adrenoceptor gene polymorphisms

    Respiratory Medicine, Vol. 100, Núm. 6, pp. 1072-1078

1997

  1. Agenesis of vas deferens and cystic fibrosis

    Actas urologicas españolas, Vol. 21, Núm. 8, pp. 773-776