Jaijo T - Search Results

1

Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I.

Jaijo T, Aller E, Oltra S, Beneyto M, Nájera C, Ayuso C, Baiget M, Carballo M, Antiñolo G, Valverde D, Moreno F, Vilela C, Perez-Garrigues H, Navea A, Millán JM. Jaijo T, et al. Hum Mutat. 2006 Mar;27(3):290-1. doi: 10.1002/humu.9404. Hum Mutat. 2006. PMID: 16470552

2

Mutation screening of USH3 gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.

Aller E, Jaijo T, Oltra S, Alió J, Galán F, Nájera C, Beneyto M, Millán JM. Aller E, et al. Among authors: jaijo t. Clin Genet. 2004 Dec;66(6):525-9. doi: 10.1111/j.1399-0004.2004.00352.x. Clin Genet. 2004. PMID: 15521980

3

[Molecular genetic study of Usher syndrome in Spain].

Jaijo T, Aller E, Beneyto M, Nájera C, Millán JM. Jaijo T, et al. Acta Otorrinolaringol Esp. 2005 Aug-Sep;56(7):285-9. doi: 10.1016/s0001-6519(05)78616-7. Acta Otorrinolaringol Esp. 2005. PMID: 16240916 Free article. Spanish.

4

Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II.

Aller E, Jaijo T, Beneyto M, Nájera C, Oltra S, Ayuso C, Baiget M, Carballo M, Antiñolo G, Valverde D, Moreno F, Vilela C, Collado D, Pérez-Garrigues H, Navea A, Millán JM. Aller E, et al. Among authors: jaijo t. J Med Genet. 2006 Nov;43(11):e55. doi: 10.1136/jmg.2006.041764. J Med Genet. 2006. PMID: 17085681 Free PMC article.

5

MYO7A mutation screening in Usher syndrome type I patients from diverse origins.

Jaijo T, Aller E, Beneyto M, Najera C, Graziano C, Turchetti D, Seri M, Ayuso C, Baiget M, Moreno F, Morera C, Perez-Garrigues H, Millan JM. Jaijo T, et al. J Med Genet. 2007 Mar;44(3):e71. doi: 10.1136/jmg.2006.045377. J Med Genet. 2007. PMID: 17361009 Free PMC article. No abstract available.

6

Screening of the USH1G gene among Spanish patients with Usher syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndrome.

Aller E, Jaijo T, Beneyto M, Nájera C, Morera C, Pérez-Garrigues H, Ayuso C, Millán J. Aller E, et al. Among authors: jaijo t. Ophthalmic Genet. 2007 Sep;28(3):151-5. doi: 10.1080/13816810701537374. Ophthalmic Genet. 2007. PMID: 17896313

7

Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I.

Oshima A, Jaijo T, Aller E, Millan JM, Carney C, Usami S, Moller C, Kimberling WJ. Oshima A, et al. Among authors: jaijo t. Hum Mutat. 2008 Jun;29(6):E37-46. doi: 10.1002/humu.20761. Hum Mutat. 2008. PMID: 18429043 Free PMC article.

8

[Genetic counselling in visual and auditory disorders].

Millán JM, Aller E, Jaijo T, Grau E, Beneyto M, Nájera C. Millán JM, et al. Among authors: jaijo t. Arch Soc Esp Oftalmol. 2008 Dec;83(12):689-702. doi: 10.4321/s0365-66912008001200003. Arch Soc Esp Oftalmol. 2008. PMID: 19085640 Review. Spanish.

9

Microarray-based mutation analysis of 183 Spanish families with Usher syndrome.

Jaijo T, Aller E, García-García G, Aparisi MJ, Bernal S, Avila-Fernández A, Barragán I, Baiget M, Ayuso C, Antiñolo G, Díaz-Llopis M, Külm M, Beneyto M, Nájera C, Millán JM. Jaijo T, et al. Invest Ophthalmol Vis Sci. 2010 Mar;51(3):1311-7. doi: 10.1167/iovs.09-4085. Epub 2009 Aug 13. Invest Ophthalmol Vis Sci. 2010. PMID: 19683999

10

The USH2A c.2299delG mutation: dating its common origin in a Southern European population.

Aller E, Larrieu L, Jaijo T, Baux D, Espinós C, González-Candelas F, Nájera C, Palau F, Claustres M, Roux AF, Millán JM. Aller E, et al. Among authors: jaijo t. Eur J Hum Genet. 2010 Jul;18(7):788-93. doi: 10.1038/ejhg.2010.14. Epub 2010 Feb 10. Eur J Hum Genet. 2010. PMID: 20145675 Free PMC article.

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