Publicacións (100) Publicacións nas que participase algún/ha investigador/a

2013

  1. A Generalized Model to Estimate the Statistical Power in Mitochondrial Disease Studies Involving 2×k Tables

    PLoS ONE, Vol. 8, Núm. 9

  2. A Xq21.31 duplication without features of Prader-Willi syndrome

    Endocrine

  3. A glimpse into past, present, and future DNA sequencing

    Molecular Genetics and Metabolism, Vol. 110, Núm. 1-2, pp. 3-24

  4. A reverse evidence of rotavirus vaccines impact

    Human Vaccines and Immunotherapeutics, Vol. 9, Núm. 6, pp. 1289-1291

  5. Actitud ante las malformaciones congénitas pulmonares

    Acta pediátrica española, Vol. 71, Núm. 8, pp. 224-232

  6. Adaptive support ventilation: State of the art review

    Indian Journal of Critical Care Medicine, Vol. 17, Núm. 1, pp. 16-22

  7. Alteración ungeal

    Cadernos de atención primaria, Vol. 19, Núm. 4, pp. 271

  8. Alternative matrices for cocaine, heroin, and methadone in utero drug exposure detection

    Therapeutic Drug Monitoring, Vol. 35, Núm. 4, pp. 502-509

  9. Ancestry analysis reveals a predominant Native American component with moderate European admixture in Bolivians

    Forensic Science International: Genetics, Vol. 7, Núm. 5, pp. 537-542

  10. Are catalase -844A/G polymorphism and activity associated with childhood obesity?

    Antioxidants and Redox Signaling, Vol. 19, Núm. 16, pp. 1970-1975

  11. Arginine-guanidinoacetate-creatine pathway in preterm newborns: Creatine biosynthesis in newborns

    Journal of Pediatric Endocrinology and Metabolism, Vol. 26, Núm. 1-2, pp. 53-60

  12. Canalización epicutánea en neonatos: una técnica no exenta de riesgos

    Metas de enfermería, Vol. 16, Núm. 9

  13. Carta dende Nablus: carácter, forza, esperanza e ganas de vivir

    Grial: revista galega de cultura, Núm. 199, pp. 120-123

  14. Cefalea infantil

    Anales de Pediatria Continuada, Vol. 11, Núm. 6, pp. 301-311

  15. Cierre percutáneo de una malformación arteriovenosa pulmonar

    Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP ), Vol. 79, Núm. 6, pp. 394-395

  16. Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening

    Molecular Genetics and Metabolism, Vol. 110, Núm. 3, pp. 218-221

  17. Clinical manifestations in female carriers of mucopolysaccharidosis type II: A spanish cross-sectional study

    Orphanet Journal of Rare Diseases, Vol. 8, Núm. 1

  18. Copper nanowires immobilized on the boards of microfluidic chips for the rapid and simultaneous diagnosis of galactosemia diseases in newborn urine samples

    Analytical Chemistry, Vol. 85, Núm. 19, pp. 9116-9125

  19. Cross-reactivity between royal jelly and dermato-phagoides pteronyssinus

    Journal of Allergy and Clinical Immunology: In Practice, Vol. 1, Núm. 2, pp. 200-201

  20. Decrease in antigen-specific CD63 basophil expression is associated with the development of tolerance to egg by SOTI in children

    Pediatric Allergy and Immunology, Vol. 24, Núm. 5, pp. 463-468