Publicaciones (405) Publicaciones en las que ha participado algún/a investigador/a

2011

  1. A child with mild X-linked intellectual disability and a microduplication at Xp22.12 including RPS6KA3

    Pediatrics, Vol. 128, Núm. 4

  2. A clean up step of fat content previous to trace metal characterization in mussel tissues by inductively coupled plasma mass spectrometry

    Microchemical Journal, Vol. 99, Núm. 2, pp. 252-259

  3. A comprehensive functional analysis of PTEN mutations: Implications in tumor- and autism-related syndromes

    Human Molecular Genetics, Vol. 20, Núm. 21, pp. 4132-4142

  4. A customized pigmentation snp array identifies a novel snp associated with melanoma predisposition in the slc45a2 gene

    PLoS ONE, Vol. 6, Núm. 4

  5. A digit symbol coding task as a screening instrument for cognitive impairment in first-episode psychosis

    Archives of Clinical Neuropsychology, Vol. 26, Núm. 1, pp. 48-58

  6. A large TAT deletion in a tyrosinaemia type II patient

    Molecular Genetics and Metabolism, Vol. 104, Núm. 3, pp. 407-409

  7. A new oral vaccine candidate based on the microencapsulation by spray-drying of inactivated Vibrio cholerae

    Vaccine, Vol. 29, Núm. 34, pp. 5758-5764

  8. A novel approach to measuring skin elasticity in systemic sclerosis: Results from a pilot study

    Scandinavian Journal of Rheumatology, Vol. 40, Núm. 3, pp. 211-216

  9. A prospective comparison of galactomannan in bronchoalveolar lavage fluid for the diagnosis of pulmonary invasive aspergillosis in medical patients under intensive care: Comparison with the diagnostic performance of galactomannan and of (1→ 3) -β-d-glucan chromogenic assay in serum samples

    Clinical Microbiology and Infection, Vol. 17, Núm. 7, pp. 1053-1060

  10. A putative "hepitype" in the ATM gene associated with chronic lymphocytic leukemia risk

    Genes Chromosomes and Cancer, Vol. 50, Núm. 11, pp. 887-895

  11. A short in-frame deletion in NTRK1 tyrosine kinase domain caused by a novel splice site mutation in a patient with congenital insensitivity to pain with anhidrosis

    BMC Medical Genetics, Vol. 12

  12. A two-stage approach to the treatment of hyperuricemia in gout: The "dirty Dish" hypothesis

    Arthritis and Rheumatism, Vol. 63, Núm. 12, pp. 4002-4006

  13. ACKNOWLEDGEMENT OF REVIEWERS

    Clinical Microbiology and Infection, Vol. 17, Núm. 1, pp. 102-103

  14. Accuracy in copy number calling by qPCR and PRT: A matter of DNA

    PLoS ONE, Vol. 6, Núm. 12

  15. Activity of soluble aminopeptidase A and dipeptidyl peptidase IV and membrane-bound aminopeptidase B and pyroglutamyl peptidase I in adenoid hyperplasia, tonsillar hyperplasia and chronic tonsillitis

    International Journal of Pediatric Otorhinolaryngology, Vol. 75, Núm. 11, pp. 1399-1403

  16. Adalimumab induction and maintenance therapy for patients with ulcerative colitis previously treated with infliximab

    Alimentary Pharmacology and Therapeutics, Vol. 33, Núm. 3, pp. 340-348

  17. Adaptation and validation of the Osteoarthritis Knee and Hip Quality of Life (OAKHQOL) questionnaire for use in patients with osteoarthritis in Spain

    Clinical Rheumatology, Vol. 30, Núm. 12, pp. 1563-1575

  18. Addressing the complexity of chronic obstructive pulmonary disease: From phenotypes and biomarkers to scale-free networks, systems biology, and P4 medicine

    American Journal of Respiratory and Critical Care Medicine, Vol. 183, Núm. 9, pp. 1129-1137

  19. Adenylate cyclase toxin promotes internalisation of integrins and raft components and decreases macrophage adhesion capacity

    PLoS ONE, Vol. 6, Núm. 2

  20. Affectively salient meaning in random noise: A task sensitive to psychosis liability

    Schizophrenia Bulletin, Vol. 37, Núm. 6, pp. 1179-1186