Universidad de Salamanca-ko ikertzaileekin lankidetzan egindako argitalpenak (3)

2015

  1. A new mutation in the COL4A3 gene responsible for autosomal dominant Alport syndrome, which only generates hearing loss in some carriers

    European Journal of Medical Genetics, Vol. 58, Núm. 1, pp. 35-38

2009

  1. Análisis genético (PKD2) de la poliquistosis renal autosómica dominante

    Nefrologia, Vol. 29, Núm. 6, pp. 562-568

1992

  1. Is Renal Protection with Calcium Antagonists Possible?

    Drugs, Vol. 44, Núm. 1, pp. 99-102