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Molecular Vision|September 16, 2005
Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVRRosa Riveiro-Alvarez, Maria José Trujillo-Tiebas, Ascension Gimenez-Pardo, et al.
Molecular Vision|March 13, 2008
Molecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosaRosa Riveiro-Alvarez, Elena Vallespin, Robert Wilke, et al.
Ophthalmology|August 25, 2012
Identification of an RP1 prevalent founder mutation and related phenotype in Spanish patients with early-onset autosomal recessive retinitisAlmudena Avila-Fernandez, Marta Corton, Koji M Nishiguchi, et al.
Investigative Ophthalmology & Visual Science|February 19, 2011
Further associations between mutations and polymorphisms in the ABCA4 gene: clinical implication of allelic variants and their role as protector/risk factorsJana Aguirre-Lamban, Juan José González-Aguilera, Rosa Riveiro-Alvarez, et al.
Pharmacogenomics|December 3, 2010
Evaluating a newly developed pharmacogenetic array: screening in a Spanish populationBerta Almoguera, Rosa Riveiro-Alvarez, Belen Gomez-Dominguez, et al.
Pharmacogenetics and Genomics|September 13, 2013
CYP2D6 poor metabolizer status might be associated with better response to risperidone treatmentBerta Almoguera, Rosa Riveiro-Alvarez, Jorge Lopez-Castroman, et al.
Orphanet Journal of Rare Diseases|February 6, 2013
High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish populationMarta Corton, Sorina D Tatu, Almudena Avila-Fernandez, et al.
Investigative Ophthalmology & Visual Science|December 7, 2007
Mutation screening of 299 Spanish families with retinal dystrophies by Leber congenital amaurosis genotyping microarrayElena Vallespin, Diego Cantalapiedra, Rosa Riveiro-Alvarez, et al.
Molecular Vision|August 7, 2008
Early noninvasive prenatal detection of a fetal CRB1 mutation causing Leber congenital amaurosisAna Bustamante-Aragones, Elena Vallespin, Marta Rodriguez de Alba, et al.
Behavioral and Brain Functions : BBF|January 10, 2016
Attention deficit hyperactivity disorder: genetic association study in a cohort of Spanish childrenClara I Gomez-Sanchez, Rosa Riveiro-Alvarez, Victor Soto-Insuga, et al.
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