Pediatría

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 glimpse into past, present, and future DNA sequencing

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

3. A reverse evidence of rotavirus vaccines impact

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

4. Actitud ante las malformaciones congénitas pulmonares

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

5. Adaptive support ventilation: State of the art review

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

6. Alteración ungeal

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

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

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

8. 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

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

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

10. 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

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

    Metas de enfermería, Vol. 16, Núm. 9

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

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

13. Cefalea infantil

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

14. 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

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

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

16. 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

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

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

18. 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

19. Detection of occult cerebrospinal fluid involvement during maintenance therapy identifies a group of children with acute lymphoblastic leukemia at high risk for relapse

    American Journal of Hematology, Vol. 88, Núm. 5, pp. 359-364

20. Displasia broncopulmonar: definiciones y clasificación

    Anales de Pediatría: Publicación Oficial de la Asociación Española de Pediatría ( AEP ), Vol. 79, Núm. 4, pp. 262