Genetic correlation between plasma levels of C4BP isoforms containing ß chains and susceptibility to thrombosis

Por Esparza-Gordillo, J, Soria, J, Buil, A, Souto, J, Almasy, L, Blangero, J, de Cordoba, S R, Fontcuberta, J
Publicado em 2004

Alkaptonuria in Italy: polymorphic haplotype background, mutational profile, and description of four novel mutations in the homogentisate 1,2-dioxygenase gene

Por PORFIRIO, B., CHIARELLI, I., GRAZIANO, C., MANNONI, A., MORRONE, A., ZAMMARCHI, E., DE BERNABE, D. B.-V., DE CORDOBA, S. R.
Publicado em 2000

Mutational analysis of the HGO gene in Finnish alkaptonuria patients

Por de Bernabe, D. B.-V., Peterson, P., Luopajarvi, K., Matintalo, P., Alho, A., Konttinen, Y., Krohn, K., de Cordoba, S. R., Ranki, A.
Publicado em 1999

Expression of the peptide C4b‐binding protein β in the arthritic joint

Por Sánchez‐Pernaute, O, Esparza‐Gordillo, J, Largo, R, Calvo, E, Alvarez‐Soria, M A, Marcos, M E, Herrero‐Beaumont, G, de Córdoba, S R
Publicado em 2006

Mutation and polymorphism analysis of the human homogentisate 1, 2-dioxygenase gene in alkaptonuria patients.

Por Beltrán-Valero de Bernabé, D, Granadino, B, Chiarelli, I, Porfirio, B, Mayatepek, E, Aquaron, R, Moore, M M, Festen, J J, Sanmartí, R, Peñalva, M A, de Córdoba, S R
Publicado em 1998