Publikationen in Zusammenarbeit mit Forschern von Hospital Vall d'Hebron (3)

2021

  1. Estándares del proceso de soporte nutricional en España: hacia el “benchmarking”

    Nutricion hospitalaria, Vol. 38, Núm. 3, pp. 661-666

2020

  1. Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

    Molecular Genetics and Genomic Medicine, Vol. 8, Núm. 11

2019

  1. Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis

    Gene, Vol. 689, pp. 227-234