Publicacións (25) Publicacións nas que participase algún/ha investigador/a

2017

  1. A replication study and meta-analysis of mitochondrial DNA variants in the radiographic progression of knee osteoarthritis

    Rheumatology (United Kingdom), Vol. 56, Núm. 2, pp. 263-270

  2. A selective screening program for the early detection of mucopolysaccharidosis: Results of the FIND project-A 2-year follow-up study

    Medicine (United States), Vol. 96, Núm. 19

  3. Anti-carbamylated protein autoantibodies associated with mortality in Spanish rheumatoid arthritis patients

    PLoS ONE, Vol. 12, Núm. 7

  4. Clinical and genetic features of 13 Spanish patients with KCNQ2 mutations

    Journal of Human Genetics, Vol. 62, Núm. 2, pp. 185-189

  5. Corrected Fructosamine improves both correlation with HbA1C and diagnostic performance

    Clinical Biochemistry, Vol. 50, Núm. 3, pp. 110-115

  6. Correlation between adenoma detection rate in colonoscopy- and fecal immunochemical testing-based colorectal cancer screening programs

    United European Gastroenterology Journal, Vol. 5, Núm. 2, pp. 255-260

  7. Defining a roadmap for harmonizing quality indicators in Laboratory Medicine: A consensus statement on behalf of the IFCC Working Group "laboratory Error and Patient Safety" and EFLM Task and Finish Group "performance specifications for the extra-analytical phases"

    Clinical Chemistry and Laboratory Medicine, Vol. 55, Núm. 10, pp. 1478-1488

  8. El goce hipocondríaco y la sociedad medicalizada

    Intercambios=Intercanvis: papers de psicoanàlisi=papeles de psicoanálisis, Núm. 39, pp. 64-66

  9. Estado de la certificación/acreditación de los laboratorios clínicos españoles: estudio inicial

    Revista del laboratorio clínico, Vol. 10, Núm. 3, pp. 139-147

  10. Evaluation of an automated commercial ELISA method for calprotectin determination in pleural fluid

    Clinical Chemistry and Laboratory Medicine

  11. Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia

    Journal of Human Genetics, Vol. 62, Núm. 3, pp. 355-360

  12. Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvement

    Neuromuscular Disorders, Vol. 27, Núm. 2, pp. 188-192

  13. Lesions in arm after a tour through the countryside

    Medicina Clinica, Vol. 149, Núm. 2, pp. e9

  14. Medición del contenido del cobre en especímenes biológicos

    Revista del laboratorio clínico, Vol. 10, Núm. 4, pp. 198-207

  15. Mitochondrial DNA haplogroups influence the risk of incident knee osteoarthritis in OAI and CHECK cohorts. A meta-Analysis and functional study

    Annals of the Rheumatic Diseases, Vol. 76, Núm. 6, pp. 1114-1122

  16. Newborn screening for Fabry disease in the north-west of Spain

    European Journal of Pediatrics, Vol. 176, Núm. 8, pp. 1075-1081

  17. Nuevos modelos para una educación científica inclusiva a través de la televisión y medios digitales

    Transformando dende a universidade: V Xornada Universitaria Galega en Xénero, XUGeX

  18. Onicomicosis subungueal proximal en paciente tratado con inhibidores del factor de necrosis tumoral alfa

    Semergen: revista española de medicina de familia, Núm. 3, pp. 245-246

  19. Pontocerebellar hypoplasia secondary to CASK gene deletion. Case report

    Revista Chilena de Pediatria, Vol. 88, Núm. 4, pp. 529-533

  20. Rewiring of the apoptotic TGF-β-SMAD/NFκB pathway through an oncogenic function of p27 in human papillary thyroid cancer

    Oncogene, Vol. 36, Núm. 5, pp. 652-666