Publicaciones en las que colabora con MARÍA ESTHER FAREZ VIDAL (12)

2013

  1. Differential immunohistochemical localization of desmosomal plaque-related proteins in non-small-cell lung cancer

    Histopathology, Vol. 63, Núm. 1, pp. 103-113

  2. Influence of CYP2D6 polymorphisms on serum levels of tamoxifen metabolites in Spanish women with breast cancer

    International Journal of Medical Sciences, Vol. 10, Núm. 7, pp. 932-937

  3. Survival, classifications, and desmosomal plaque genes in non-small cell lung cancer

    International Journal of Medical Sciences, Vol. 10, Núm. 9, pp. 1166-1173

2012

  1. Multiplex primer extension reaction and capillary electrophoresis to study the frequency of thrombophilia-related mutations in a spanish population

    Clinica Chimica Acta, Vol. 413, Núm. 15-16, pp. 1255-1258

2011

  1. Gene expression profiling reveals novel biomarkers in nonsmall cell lung cancer

    International Journal of Cancer, Vol. 129, Núm. 2, pp. 355-364

2010

  1. Gene expression signatures in breast cancer distinguish phenotype characteristics, histologic subtypes, and tumor invasiveness

    Cancer, Vol. 116, Núm. 2, pp. 486-496

2008

  1. A family with atypical cystic fibrosis: brother and sister with heterozygosity for both G542X and R117H

    Pediatric and Developmental Pathology, Vol. 11, Núm. 3, pp. 213-219

  2. Multi-mutational analysis of fifteen common mutations of the glucose 6-phosphate dehydrogenase gene in the Mediterrranean population

    Clinica Chimica Acta, Vol. 395, Núm. 1-2, pp. 94-98

  3. Use of capillary electrophoresis for accurate determination of CAG repeats causing Huntington disease. An oligonucleotide design avoiding shadow bands

    Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 68, Núm. 7, pp. 577-584

2005

  1. Frequency and clinical expression of HFE gene mutations in a Spanish population of subjects with abnormal iron metabolism

    Annals of Hematology, Vol. 84, Núm. 10, pp. 650-655

2004

  1. Multimutational analysis of eleven cystic fibrosis mutations common in the Mediterranean areas

    Clinical Chemistry, Vol. 50, Núm. 11, pp. 2155-2157

  2. Multiplex analysis of the most common mutations related to hereditary haemochromatosis: Two methods combining specific amplification with capillary electrophoresis

    European Journal of Haematology, Vol. 72, Núm. 2, pp. 121-129