Publicacións (24) Publicacións nas que participase algún/ha investigador/a

2011

  1. A limited sampling strategy for estimation of the area under the curve (0 to 8 hours) of mycophenolic acid administered three times daily to liver transplant recipients

    Upsala Journal of Medical Sciences, Vol. 116, Núm. 1, pp. 47-51

  2. Aspergilosis pulmonar necrotizante crónica como complicación de silicosis

    Anales del sistema sanitario de Navarra, Vol. 34, Núm. 1, pp. 109-114

  3. Chondrogenic differentiation of human bone marrow mesenchymal stem cells in PEPMHA hydrogels

    24th European Conference on Biomaterials - Annual Conference of the European Society for Biomaterials

  4. Clinical validation of cutoff target ranges in newborn screening of metabolic disorders by tandem mass spectrometry: A worldwide collaborative project

    Genetics in Medicine, Vol. 13, Núm. 3, pp. 230-254

  5. Congenital hypothyroidism with neurological and respiratory alterations: A case detected using a variable diagnostic threshold for Tsh

    JCRPE Journal of Clinical Research in Pediatric Endocrinology, Vol. 3, Núm. 4, pp. 208-211

  6. Construction and phenotypic characterization of HIV type 1 functional envelope clones of subtypes G and F

    AIDS Research and Human Retroviruses, Vol. 27, Núm. 8, pp. 889-901

  7. Determination of blood everolimus concentrations in kidney and liver transplant recipients using the sirolimus antibody conjugated magnetic immunoassay (ACMIA)

    Clinical Laboratory, Vol. 57, Núm. 5-6, pp. 403-406

  8. Doublecortin is expressed in trigeminal motoneurons that innervate the velar musculature of lampreys: Considerations on the evolution and development of the trigeminal system

    Evolution and Development, Vol. 13, Núm. 2, pp. 149-158

  9. Effect of alcohol consumption and cessation on serum total immunoglobulin E concentrations

    Journal of Investigational Allergology and Clinical Immunology

  10. Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme

    Molecular Genetics and Metabolism, Vol. 104, Núm. 4, pp. 470-475

  11. Hepatoerythropoietic porphyria due to a novel mutation in the uroporphyrinogen decarboxylase gene

    British Journal of Dermatology, Vol. 165, Núm. 3, pp. 499-505

  12. Immunoglobulin heavy chains in medaka (Oryzias latipes)

    BMC Evolutionary Biology, Vol. 11, Núm. 1

  13. Inborn errors of metabolism in a neonatology unit: Impact and long-term results

    Pediatrics International, Vol. 53, Núm. 1, pp. 13-17

  14. LIF, a novel STAT5-regulated gene, is aberrantly expressed in myeloproliferative neoplasms

    Genes and Cancer, Vol. 2, Núm. 5, pp. 593-596

  15. Macromolecular complexes of cystatin C with circulating liver plasma membrane fragments and determination of serum cystatin C using the particle enhanced nephelometric immunoassay (PENIA) in kidney and liver transplantation and biliary obstruction

    Clinical Laboratory, Vol. 57, Núm. 3-4, pp. 207-212

  16. Model predicting survival / exitus after traumatic brain injury: Biomarker S100B 24H

    Clinical Laboratory, Vol. 57, Núm. 7-8, pp. 587-597

  17. Pituitary stalk dysgenesis-induced hypopituitarism in adult patients: Prevalence, evolution of hormone dysfunction and genetic analysis

    Neuroendocrinology, Vol. 93, Núm. 3, pp. 181-188

  18. Progression of nephropathy in type 2 diabetes: The glycation gap is a significant predictor after adjustment for glycohemoglobin (Hb A1c)

    Clinical Chemistry, Vol. 57, Núm. 2, pp. 264-271

  19. The TSH threshold in neonatal screening for congenital hypothyroidism: A variable solution

    Archives of Disease in Childhood, Vol. 96, Núm. 6, pp. 565-566

  20. The influence of valproic acid and carbamazepine treatment on serum biotin and zinc levels and on biotinidase activity

    Journal of Child Neurology