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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2005 8
2006 12
2007 13
2008 18
2009 7
2010 8
2011 3
2013 2
2019 2
2021 2
2024 0

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72 results

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Page 1
Outcome of ABCA4 disease-associated alleles in autosomal recessive retinal dystrophies: retrospective analysis in 420 Spanish families.
Riveiro-Alvarez R, Lopez-Martinez MA, Zernant J, Aguirre-Lamban J, Cantalapiedra D, Avila-Fernandez A, Gimenez A, Lopez-Molina MI, Garcia-Sandoval B, Blanco-Kelly F, Corton M, Tatu S, Fernandez-San Jose P, Trujillo-Tiebas MJ, Ramos C, Allikmets R, Ayuso C. Riveiro-Alvarez R, et al. Among authors: cantalapiedra d. Ophthalmology. 2013 Nov;120(11):2332-7. doi: 10.1016/j.ophtha.2013.04.002. Epub 2013 Jun 4. Ophthalmology. 2013. PMID: 23755871 Free PMC article.
Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications.
Perea-Romero I, Gordo G, Iancu IF, Del Pozo-Valero M, Almoguera B, Blanco-Kelly F, Carreño E, Jimenez-Rolando B, Lopez-Rodriguez R, Lorda-Sanchez I, Martin-Merida I, Pérez de Ayala L, Riveiro-Alvarez R, Rodriguez-Pinilla E, Tahsin-Swafiri S, Trujillo-Tiebas MJ; ESRETNET Study Group; ERDC Study Group; Associated Clinical Study Group; Garcia-Sandoval B, Minguez P, Avila-Fernandez A, Corton M, Ayuso C. Perea-Romero I, et al. Sci Rep. 2021 Jan 15;11(1):1526. doi: 10.1038/s41598-021-81093-y. Sci Rep. 2021. PMID: 33452396 Free PMC article.
Late onset retinitis pigmentosa.
Avila-Fernández A, Cortón M, López-Molina MI, Martín-Garrido E, Cantalapiedra D, Fernández-Sánchez R, Blanco-Kelly F, Riveiro-Álvarez R, Tatu SD, Trujillo-Tiebas MJ, García-Sandoval B, Ayuso C, Cremers FP. Avila-Fernández A, et al. Among authors: cantalapiedra d. Ophthalmology. 2011 Dec;118(12):2523-4. doi: 10.1016/j.ophtha.2011.07.030. Ophthalmology. 2011. PMID: 22136677 No abstract available.
Frequency of ABCA4 mutations in 278 Spanish controls: an insight into the prevalence of autosomal recessive Stargardt disease.
Riveiro-Alvarez R, Aguirre-Lamban J, Lopez-Martinez MA, Trujillo-Tiebas MJ, Cantalapiedra D, Vallespin E, Avila-Fernandez A, Ramos C, Ayuso C. Riveiro-Alvarez R, et al. Among authors: cantalapiedra d. Br J Ophthalmol. 2009 Oct;93(10):1359-64. doi: 10.1136/bjo.2008.148155. Epub 2008 Oct 31. Br J Ophthalmol. 2009. PMID: 18977788 Free PMC article. Review.
Gene symbol: CRB1.
Vallespin E, Riveiro-Alvarez R, Cantalapiedra D, Aguirre-Lambam J, Avila-Fernandez A, Lopez-Martinez MA, Gallego-Merlo J, Trujillo-Tiebas MJ, Ayuso C. Vallespin E, et al. Among authors: cantalapiedra d. Hum Genet. 2007 Apr;121(2):287-8. Hum Genet. 2007. PMID: 17598198 No abstract available.
Are there enough radiation oncologists to lead the new Spanish radiotherapy?
Rodríguez A, Arenas M, Lara PC, López-Torrecilla J, Algara M, Conde A, Pérez-Montero H, Muñoz JL, Peleteiro P, Pérez-Calatayud MJ, Contreras J, Ferrer C; Spanish Society of Oncology and Radiotherapy (SEOR) Analysis Group. Rodríguez A, et al. Clin Transl Oncol. 2019 Dec;21(12):1663-1672. doi: 10.1007/s12094-019-02095-x. Epub 2019 Apr 3. Clin Transl Oncol. 2019. PMID: 30941701
Gene symbol: CRB1.
Vallespin E, Riveiro-Alvarez R, Cantalapiedra D, Aguirre-Lambam J, Avila-Fernandez A, Lopez-Gimenez-Pardo A, Trujillo-Tiebas MJ, Ayuso C. Vallespin E, et al. Among authors: cantalapiedra d. Hum Genet. 2007 Apr;121(2):297-8. Hum Genet. 2007. PMID: 17598245 No abstract available.
Gene symbol: CRB1.
Vallespin E, Millan JM, Riveiro-Alvarez R, Aguirre-Lamban J, Cantalapiedra D, Gallego J, Trujillo-Tiebas MJ, Ayuso C. Vallespin E, et al. Among authors: cantalapiedra d. Hum Genet. 2007 Feb;120(6):914. Hum Genet. 2007. PMID: 17438615 No abstract available.
Evaluation of SFRP1 as a candidate for human retinal dystrophies.
Garcia-Hoyos M, Cantalapiedra D, Arroyo C, Esteve P, Rodríguez J, Riveiro R, Trujillo MJ, Ramos C, Bovolenta P, Ayuso C. Garcia-Hoyos M, et al. Among authors: cantalapiedra d. Mol Vis. 2004 Jun 28;10:426-31. Mol Vis. 2004. PMID: 15235574 Free article.
72 results