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Year | Number of Results |
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2011 | 1 |
2013 | 3 |
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Page 1
Late onset retinitis pigmentosa.
Ophthalmology. 2011 Dec;118(12):2523-4. doi: 10.1016/j.ophtha.2011.07.030.
Ophthalmology. 2011.
PMID: 22136677
No abstract available.
Exome sequencing of index patients with retinal dystrophies as a tool for molecular diagnosis.
Corton M, Nishiguchi KM, Avila-Fernández A, Nikopoulos K, Riveiro-Alvarez R, Tatu SD, Ayuso C, Rivolta C.
Corton M, et al. Among authors: tatu sd.
PLoS One. 2013 Jun 14;8(6):e65574. doi: 10.1371/journal.pone.0065574. Print 2013.
PLoS One. 2013.
PMID: 23940504
Free PMC article.
Item in Clipboard
High frequency of CRB1 mutations as cause of Early-Onset Retinal Dystrophies in the Spanish population.
Corton M, Tatu SD, Avila-Fernandez A, Vallespín E, Tapias I, Cantalapiedra D, Blanco-Kelly F, Riveiro-Alvarez R, Bernal S, García-Sandoval B, Baiget M, Ayuso C.
Corton M, et al. Among authors: tatu sd.
Orphanet J Rare Dis. 2013 Feb 5;8:20. doi: 10.1186/1750-1172-8-20.
Orphanet J Rare Dis. 2013.
PMID: 23379534
Free PMC article.
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Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population.
Corton M, Avila-Fernandez A, Vallespín E, López-Molina MI, Almoguera B, Martín-Garrido E, Tatu SD, Khan MI, Blanco-Kelly F, Riveiro-Alvarez R, Brión M, García-Sandoval B, Cremers FPM, Carracedo A, Ayuso C.
Corton M, et al. Among authors: tatu sd.
Ophthalmology. 2014 Jan;121(1):399-407. doi: 10.1016/j.ophtha.2013.08.028. Epub 2013 Oct 18.
Ophthalmology. 2014.
PMID: 24144451
Item in Clipboard
Contribution of mutation load to the intrafamilial genetic heterogeneity in a large cohort of Spanish retinal dystrophies families.
Sánchez-Alcudia R, Cortón M, Ávila-Fernández A, Zurita O, Tatu SD, Pérez-Carro R, Fernandez-San Jose P, Lopez-Martinez MÁ, del Castillo FJ, Millan JM, Blanco-Kelly F, García-Sandoval B, Lopez-Molina MI, Riveiro-Alvarez R, Ayuso C.
Sánchez-Alcudia R, et al. Among authors: tatu sd.
Invest Ophthalmol Vis Sci. 2014 Oct 23;55(11):7562-71. doi: 10.1167/iovs.14-14938.
Invest Ophthalmol Vis Sci. 2014.
PMID: 25342620
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Correction: Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis.
Corton M, Nishiguchi KM, Avila-Fernández A, Nikopoulos K, Riveiro-Alvarez R, Tatu SD, Ayuso C, Rivolta C.
Corton M, et al. Among authors: tatu sd.
PLoS One. 2016 Mar 31;11(3):e0153121. doi: 10.1371/journal.pone.0153121. eCollection 2016.
PLoS One. 2016.
PMID: 27031522
Free PMC article.
No abstract available.
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