Servicio
Análises clínicas
Publicacións (24) Publicacións nas que participase algún/ha investigador/a
2011
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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
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Aspergilosis pulmonar necrotizante crónica como complicación de silicosis
Anales del sistema sanitario de Navarra, Vol. 34, Núm. 1, pp. 109-114
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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
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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
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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
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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
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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
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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
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Effect of alcohol consumption and cessation on serum total immunoglobulin E concentrations
Journal of Investigational Allergology and Clinical Immunology
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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
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Hepatoerythropoietic porphyria due to a novel mutation in the uroporphyrinogen decarboxylase gene
British Journal of Dermatology, Vol. 165, Núm. 3, pp. 499-505
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Immunoglobulin heavy chains in medaka (Oryzias latipes)
BMC Evolutionary Biology, Vol. 11, Núm. 1
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Inborn errors of metabolism in a neonatology unit: Impact and long-term results
Pediatrics International, Vol. 53, Núm. 1, pp. 13-17
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LIF, a novel STAT5-regulated gene, is aberrantly expressed in myeloproliferative neoplasms
Genes and Cancer, Vol. 2, Núm. 5, pp. 593-596
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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
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Model predicting survival / exitus after traumatic brain injury: Biomarker S100B 24H
Clinical Laboratory, Vol. 57, Núm. 7-8, pp. 587-597
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Pituitary stalk dysgenesis-induced hypopituitarism in adult patients: Prevalence, evolution of hormone dysfunction and genetic analysis
Neuroendocrinology, Vol. 93, Núm. 3, pp. 181-188
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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
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The TSH threshold in neonatal screening for congenital hypothyroidism: A variable solution
Archives of Disease in Childhood, Vol. 96, Núm. 6, pp. 565-566
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The influence of valproic acid and carbamazepine treatment on serum biotin and zinc levels and on biotinidase activity
Journal of Child Neurology