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

Year Number of Results
1988 2
1989 1
1990 1
2001 1
2002 3
2007 1
2008 2
2009 1
2011 1
2012 1
2013 1
2014 1
2017 2
2018 1
2021 0
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16 results
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Page 1
Knotting dynamics during DNA replication.
Olavarrieta L, Martínez-Robles ML, Hernández P, Krimer DB, Schvartzman JB. Olavarrieta L, et al. Mol Microbiol. 2002 Nov;46(3):699-707. doi: 10.1046/j.1365-2958.2002.03217.x. Mol Microbiol. 2002. PMID: 12410827 Free article.
Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration.
Martínez-Barricarte R, Recalde S, Fernández-Robredo P, Millán I, Olavarrieta L, Viñuela A, Pérez-Pérez J, García-Layana A, Rodríguez de Córdoba S; Spanish Multicenter Group on AMD. Martínez-Barricarte R, et al. Among authors: olavarrieta l. Invest Ophthalmol Vis Sci. 2012 Mar 1;53(3):1087-94. doi: 10.1167/iovs.11-8709. Invest Ophthalmol Vis Sci. 2012. PMID: 22247456 Free article.
Association between CFH, CFB, ARMS2, SERPINF1, VEGFR1 and VEGF polymorphisms and anatomical and functional response to ranibizumab treatment in neovascular age-related macular degeneration.
Cobos E, Recalde S, Anter J, Hernandez-Sanchez M, Barreales C, Olavarrieta L, Valverde A, Suarez-Figueroa M, Cruz F, Abraldes M, Pérez-Pérez J, Fernández-Robredo P, Arias L, García-Layana A. Cobos E, et al. Among authors: olavarrieta l. Acta Ophthalmol. 2018 Mar;96(2):e201-e212. doi: 10.1111/aos.13519. Epub 2017 Sep 19. Acta Ophthalmol. 2018. PMID: 28926193 Free article.
Giant inguino-scrotal bladder hernia. Report of a case.
Peiró F, Zaragozá C, Castaño S, Olavarrieta L, García-Aguado R, Vivó M. Peiró F, et al. Among authors: olavarrieta l. Ambul Surg. 2001 Jan;9(1):23-24. doi: 10.1016/s0966-6532(00)00068-8. Ambul Surg. 2001. PMID: 11179709
[Mucinous cystadenocarcinoma of the appendix].
Del Rosal R, Zaragoza C, Dávila D, Medrano J, Diestro G, Olavarrieta L, Narbona B. Del Rosal R, et al. Among authors: olavarrieta l. Rev Esp Enferm Apar Dig. 1988 Oct;74(4 Pt 1):361-2. Rev Esp Enferm Apar Dig. 1988. PMID: 3231872 Spanish. No abstract available.
Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane.
Legan PK, Goodyear RJ, Morín M, Mencia A, Pollard H, Olavarrieta L, Korchagina J, Modamio-Hoybjor S, Mayo F, Moreno F, Moreno-Pelayo MA, Richardson GP. Legan PK, et al. Among authors: olavarrieta l. Hum Mol Genet. 2014 May 15;23(10):2551-68. doi: 10.1093/hmg/ddt646. Epub 2013 Dec 20. Hum Mol Genet. 2014. PMID: 24363064 Free PMC article.
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Hildebrand MS, Morín M, Meyer NC, Mayo F, Modamio-Hoybjor S, Mencía A, Olavarrieta L, Morales-Angulo C, Nishimura CJ, Workman H, DeLuca AP, del Castillo I, Taylor KR, Tompkins B, Goodman CW, Schrauwen I, Wesemael MV, Lachlan K, Shearer AE, Braun TA, Huygen PL, Kremer H, Van Camp G, Moreno F, Casavant TL, Smith RJ, Moreno-Pelayo MA. Hildebrand MS, et al. Among authors: olavarrieta l. Hum Mutat. 2011 Jul;32(7):825-34. doi: 10.1002/humu.21512. Epub 2011 Jun 7. Hum Mutat. 2011. PMID: 21520338 Free PMC article.
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