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Clinical analysis
Publications (25) Publications in which a researcher has participated
2017
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A replication study and meta-analysis of mitochondrial DNA variants in the radiographic progression of knee osteoarthritis
Rheumatology (United Kingdom), Vol. 56, Núm. 2, pp. 263-270
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A selective screening program for the early detection of mucopolysaccharidosis: Results of the FIND project-A 2-year follow-up study
Medicine (United States), Vol. 96, Núm. 19
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Anti-carbamylated protein autoantibodies associated with mortality in Spanish rheumatoid arthritis patients
PLoS ONE, Vol. 12, Núm. 7
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Clinical and genetic features of 13 Spanish patients with KCNQ2 mutations
Journal of Human Genetics, Vol. 62, Núm. 2, pp. 185-189
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Corrected Fructosamine improves both correlation with HbA1C and diagnostic performance
Clinical Biochemistry, Vol. 50, Núm. 3, pp. 110-115
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Correlation between adenoma detection rate in colonoscopy- and fecal immunochemical testing-based colorectal cancer screening programs
United European Gastroenterology Journal, Vol. 5, Núm. 2, pp. 255-260
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Defining a roadmap for harmonizing quality indicators in Laboratory Medicine: A consensus statement on behalf of the IFCC Working Group "laboratory Error and Patient Safety" and EFLM Task and Finish Group "performance specifications for the extra-analytical phases"
Clinical Chemistry and Laboratory Medicine, Vol. 55, Núm. 10, pp. 1478-1488
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El goce hipocondríaco y la sociedad medicalizada
Intercambios=Intercanvis: papers de psicoanàlisi=papeles de psicoanálisis, Núm. 39, pp. 64-66
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Estado de la certificación/acreditación de los laboratorios clínicos españoles: estudio inicial
Revista del laboratorio clínico, Vol. 10, Núm. 3, pp. 139-147
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Evaluation of an automated commercial ELISA method for calprotectin determination in pleural fluid
Clinical Chemistry and Laboratory Medicine
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Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia
Journal of Human Genetics, Vol. 62, Núm. 3, pp. 355-360
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Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvement
Neuromuscular Disorders, Vol. 27, Núm. 2, pp. 188-192
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Lesions in arm after a tour through the countryside
Medicina Clinica, Vol. 149, Núm. 2, pp. e9
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Medición del contenido del cobre en especímenes biológicos
Revista del laboratorio clínico, Vol. 10, Núm. 4, pp. 198-207
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Mitochondrial DNA haplogroups influence the risk of incident knee osteoarthritis in OAI and CHECK cohorts. A meta-Analysis and functional study
Annals of the Rheumatic Diseases, Vol. 76, Núm. 6, pp. 1114-1122
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Newborn screening for Fabry disease in the north-west of Spain
European Journal of Pediatrics, Vol. 176, Núm. 8, pp. 1075-1081
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Nuevos modelos para una educación científica inclusiva a través de la televisión y medios digitales
Transformando dende a universidade: V Xornada Universitaria Galega en Xénero, XUGeX
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Onicomicosis subungueal proximal en paciente tratado con inhibidores del factor de necrosis tumoral alfa
Semergen: revista española de medicina de familia, Núm. 3, pp. 245-246
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Pontocerebellar hypoplasia secondary to CASK gene deletion. Case report
Revista Chilena de Pediatria, Vol. 88, Núm. 4, pp. 529-533
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Rewiring of the apoptotic TGF-β-SMAD/NFκB pathway through an oncogenic function of p27 in human papillary thyroid cancer
Oncogene, Vol. 36, Núm. 5, pp. 652-666