Prevention of bleeding after percutaneous biopsy with a small intestinal submucosa hemostatic plug.

Screening of CNVs using NGS data improves mutation detection yield and decreases costs in genetic testing for hereditary cancer.

Variants of uncertain significance (VUS) in cancer predisposing genes: What are we learning from multigene panels?

RNA assay identifies a previous misclassification of BARD1 c.1977A>G variant.

International consensus on clinical severity scale use in evaluating Niemann-Pick disease Type C in paediatric and adult patients: results from a Delphi Study.

CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools.

Postoperative outcomes in oesophagectomy with trainee involvement.

Suppression of inflammatory arthritis by the parasitic worm product ES-62 is associated with epigenetic changes in synovial fibroblasts.

Plasma idebenone monitoring in Friedreich's ataxia patients during a long-term follow-up.

Paired Somatic-Germline Testing of 15 Polyposis and Colorectal Cancer-Predisposing Genes Highlights the Role of APC Mosaicism in de Novo Familial Adenomatous Polyposis.

Description of the molecular and clinical characteristics of the mucopolysaccharidosis type VII Iberian cohort.

The Genetic Landscape of Mitochondrial Diseases in Spain: A Nationwide Call.

Efficacy and safety of tivozanib in recurrent, platinum-resistant ovarian, fallopian tube or primary peritoneal cancer, an NCCN phase II trial.

Sensitivity of cervical cytology in endometrial cancer detection in a tertiary hospital in Spain.

Evaluation of Sodium Bisulfate on Reducing Salmonella Heidelberg Biofilm and Colonization in Broiler Crops and Ceca.