Publikationen in Zusammenarbeit mit Forschern von Hospital Clínico San Carlos de Madrid (5)

2022

  1. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients

    Orphanet Journal of Rare Diseases, Vol. 17, Núm. 1

2018

  1. Pain assessment in mechanically ventilated, noncommunicative severe trauma patients

    Journal of Trauma Nursing, Vol. 25, Núm. 1, pp. 49-59

2015

  1. Recommendations for somatic and germline genetic testing of single pheochromocytoma and paraganglioma based on findings from a series of 329 patients

    Journal of Medical Genetics, Vol. 52, Núm. 10, pp. 647-656

2012

  1. Shorter telomere length is associated with increased: Ovarian cancer risk in both familial and sporadic cases

    Journal of Medical Genetics, Vol. 49, Núm. 5, pp. 341-344

2011

  1. Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma

    Nature Genetics