Publicaciones (398) Publicaciones en las que ha participado algún/a investigador/a

2008

  1. "Made in" operadores: Geodis-Akzo Nobel

    Logística integral: la cadena de suministro sin fronteras, Núm. 51, pp. 24-27

  2. 2006 GEP-ISFG collaborative exercise on mtDNA: reflections about interpretation, artefacts, and DNA mixtures

    Forensic Science International: Genetics, Vol. 2, Núm. 2, pp. 126-133

  3. 2ª mesa redonda: el presente y el futuro de la neumología

    Revista española de patología torácica, Vol. 20, Núm. 1, pp. 11-13

  4. A 12-month, open-label, comparative study of quetiapine and risperidone in the acute and long-term treatment of schizophrenia

    International Clinical Psychopharmacology, Vol. 23, Núm. 3, pp. 138-149

  5. A 12-week aerobic training program reduced serum C-reactive protein in women with metabolic syndrome

    Archives of Hellenic Medicine, Vol. 25, Núm. 3, pp. 363-366

  6. A Mediterranean Dietary Style Improves Calcium Utilization in Healthy Male Adolescents

    Journal of the American College of Nutrition, Vol. 27, Núm. 4, pp. 454-462

  7. A controlled study of the time-course of breath alcohol concentration after moderate ingestion of ethanol following a social drinking session

    Forensic Science International, Vol. 177, Núm. 2-3, pp. 140-145

  8. A descriptive case-register study of delusional disorder

    European Psychiatry, Vol. 23, Núm. 2, pp. 125-133

  9. A digenic combination of polymorphisms within ESR1 and ESR2 genes are associated with age at menarche in the Spanish population

    Reproductive Sciences, Vol. 15, Núm. 3, pp. 305-311

  10. A family with atypical cystic fibrosis: brother and sister with heterozygosity for both G542X and R117H

    Pediatric and Developmental Pathology, Vol. 11, Núm. 3, pp. 213-219

  11. A fatal case following exposure to zinc chloride and hexachloroethane from a smoke bomb in a fire simulation at a school

    Clinical Toxicology, Vol. 46, Núm. 6, pp. 563-565

  12. A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus

    Human Molecular Genetics, Vol. 18, Núm. 3, pp. 569-579

  13. A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy

    Human Mutation, Vol. 29, Núm. 6, pp. 823-831

  14. A numerical comparison of several unconditional exact tests in problems of equivalence based on the difference of proportions

    Journal of Statistical Computation and Simulation, Vol. 78, Núm. 11, pp. 969-981

  15. A patient with persistent hiccups and gastro-oesophageal reflux disease

    Gut, Vol. 57, Núm. 6

  16. A real-time spiking cerebellum model for learning robot control

    BioSystems, Vol. 94, Núm. 1-2, pp. 18-27

  17. A role for p38α mitogen-activated protein kinase in embryonic cardiac differentiation

    FEBS Letters, Vol. 582, Núm. 7, pp. 1025-1031

  18. A systematic review of tests for lymph node status in primary endometrial cancer

    BMC Women's Health, Vol. 8

  19. ADCK3, an Ancestral Kinase, Is Mutated in a Form of Recessive Ataxia Associated with Coenzyme Q10 Deficiency

    American Journal of Human Genetics, Vol. 82, Núm. 3, pp. 661-672

  20. Accuracy of mean arterial pressure and blood pressure measurements in predicting pre-eclampsia: systematic review and meta-analysis

    BMJ-BRITISH MEDICAL JOURNAL, Vol. 336, Núm. 7653, pp. 1117-1120