JOSÉ MARÍA
LADERO QUESADA
Investigador hasta 2015
Publicaciones (136) Publicaciones de JOSÉ MARÍA LADERO QUESADA
2021
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Genetic variants of alcohol metabolizing enzymes and alcohol-related liver cirrhosis risk
Journal of Personalized Medicine, Vol. 11, Núm. 5
2016
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GC gene polymorphism and unbound serum retinol-binding protein 4 are related to the risk of insulin resistance in patients with chronic hepatitis c: A prospective cross-sectional study
Medicine (United States), Vol. 95, Núm. 10
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The relation of fibrosis stage with nutritional deficiencies and bioelectrical impedance analysis of body composition in patients with chronic hepatitis C
Annals of Hepatology, Vol. 15, Núm. 4, pp. 492-500
2015
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Matrix Metalloproteinase 10 Contributes To Hepatocarcinogenesis in a Novel Crosstalk With the Stromal Derived Factor 1/C-X-C Chemokine Receptor 4 Axis
Hepatology, Vol. 62, Núm. 1, pp. 166-178
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Transarterial chemoembolisation in intermediate-Stage hepatocellular carcinoma. Survey on clinical practice in hospitals in the Madrid Region
Annals of Hepatology, Vol. 14, Núm. 2, pp. 207-217
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Undetectable HCV-RNA at treatment-week 8 results in high-sustained virological response in HCV G1 treatment-experienced patients with advanced liver disease: The International Italian/Spanish Boceprevir/Peginterferon/Ribavirin Name Patients Program
Journal of Viral Hepatitis, Vol. 22, Núm. 5, pp. 469-480
2013
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Influence of Vitamin D-Related Gene Polymorphisms (CYP27B and VDR) on the Response to Interferon/Ribavirin Therapy in Chronic Hepatitis C
PLoS ONE, Vol. 8, Núm. 9
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Sorafenib for non-selected patient population with advanced hepatocellular carcinoma: Efficacy and safety data according to liver function
Clinical and Translational Oncology, Vol. 15, Núm. 2, pp. 146-153
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Vitamin D deficiency and vitamin D therapy in chronic hepatitis C
Annals of Hepatology, Vol. 12, Núm. 2, pp. 199-204
2012
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Analysis of the functional polymorphism in the cytochrome P450 CYP2C8 gene rs11572080 with regard to colorectal cancer risk
Frontiers in Genetics, Vol. 3, Núm. DEC
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Hyperuricemia and metabolic syndrome in children with overweight and obesity
Endocrinología y nutrición: órgano de la Sociedad Española de Endocrinología y Nutrición, Vol. 59, Núm. 9, pp. 533-538
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Polymorphism of the TLR4 gene reduces the risk of hepatitis C virus-induced hepatocellular carcinoma
Oncology, Vol. 82, Núm. 1, pp. 35-40
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Predicting response to therapy in chronic hepatitis C: An approach combining interleukin-28B gene polymorphisms and clinical data
Journal of Gastroenterology and Hepatology (Australia), Vol. 27, Núm. 2, pp. 279-285
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Relation of IL28b gene polymorphism with biochemical and histological features in hepatitis C virus-induced liver disease
PLoS ONE, Vol. 7, Núm. 5
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Serum cystatin C: A non-invasive marker of liver fibrosis or of current liver fibrogenesis in chronic hepatitis C?
Annals of Hepatology, Vol. 11, Núm. 5, pp. 648-651
2011
2010
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CYP2W1 variant alleles in Caucasians and association of the CYP2W1 G541A (Ala181Thr) polymorphism with increased colorectal cancer risk
Pharmacogenomics, Vol. 11, Núm. 7, pp. 919-925
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Non-invasive evaluation of the fibrosis stage in chronic hepatitis C: A comparative analysis of nine scoring methods
Scandinavian Journal of Gastroenterology, Vol. 45, Núm. 1, pp. 51-59
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Tratamiento de la hepatitis crónica C: situación actual y perspectivas
Anales de la Real Academia Nacional de Medicina, Núm. 3, pp. 413-433
2009
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Analysis of a non-synonymous single nucleotide polymorphism of the human diamine oxidase gene (ref. SNP ID: Rs1049793) in patients with Crohn's disease
Scandinavian Journal of Gastroenterology, Vol. 44, Núm. 10, pp. 1207-1212