Publikationen in Zusammenarbeit mit Forschern von Hospital Clinic Barcelona (13)

2023

  1. Expression of HMGCS2 in intestinal epithelial cells is downregulated in inflammatory bowel disease associated with endoplasmic reticulum stress

    Frontiers in immunology, Vol. 14, pp. 1185517

  2. Local recurrence and metastatic disease in pheochromocytomas and sympathetic paragangliomas

    Frontiers in Endocrinology, Vol. 14

  3. Neuroblastoma RAS viral oncogene homolog (N-RAS) deficiency aggravates liver injury and fibrosis

    Cell death & disease, Vol. 14, Núm. 8, pp. 514

2022

  1. The insecticides permethrin and chlorpyrifos show limited genotoxicity and no leukemogenic potential in human and murine hematopoietic stem progenitor cells

    Haematologica

  2. Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals

    Frontiers in Genetics, Vol. 13

2021

  1. Abnormal liver function test in patients infected with coronavirus (Sars-cov-2): A retrospective single-center study from spain

    Journal of Clinical Medicine, Vol. 10, Núm. 5, pp. 1-18

2019

  1. Author Correction: Combination of KIR2DS4 and FcγRIIa polymorphisms predicts the response to cetuximab in KRAS mutant metastatic colorectal cancer (Scientific Reports, (2019), 9, 1, (2589), 10.1038/s41598-019-39291-2)

    Scientific Reports

  2. Combination of KIR2DS4 and FcγRIIa polymorphisms predicts the response to cetuximab in KRAS mutant metastatic colorectal cancer

    Scientific Reports, Vol. 9, Núm. 1

2013

  1. A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability

    Gene, Vol. 521, Núm. 1, pp. 82-86

2011

  1. Multiple platform assessment of the EGF dependent transcriptome by microarray and deep tag sequencing analysis

    BMC Genomics, Vol. 12

2007

  1. Contiguous deletion of the NDP, MAOA, MAOB and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy

    American Journal of Medical Genetics, Part A, Vol. 143, Núm. 9, pp. 916-920

  2. X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation

    BMC Genomics, Vol. 8

2000

  1. Radiofrequency ablation of a posteroseptal atrioventricular accessory pathway in a left-sided tricuspid ring with Ebsteinlike anomaly in a patient with congenitally corrected transposition of the great arteries

    PACE - Pacing and Clinical Electrophysiology, Vol. 23, Núm. 1, pp. 133-136