Baiget M - Search Results

1

Molecular approach in the study of Alström syndrome: analysis of ten Spanish families.

Piñeiro-Gallego T, Cortón M, Ayuso C, Baiget M, Valverde D. Piñeiro-Gallego T, et al. Among authors: baiget m. Mol Vis. 2012;18:1794-802. Epub 2012 Jul 3. Mol Vis. 2012. PMID: 22876109 Free PMC article.

2

New mutations in BBS genes in small consanguineous families with Bardet-Biedl syndrome: detection of candidate regions by homozygosity mapping.

Pereiro I, Valverde D, Piñeiro-Gallego T, Baiget M, Borrego S, Ayuso C, Searby C, Nishimura D. Pereiro I, et al. Among authors: baiget m. Mol Vis. 2010 Feb 1;16:137-43. Mol Vis. 2010. PMID: 20142850 Free PMC article.

3

Microarray-based mutation analysis of the ABCA4 gene in Spanish patients with Stargardt disease: evidence of a prevalent mutated allele.

Valverde D, Riveiro-Alvarez R, Bernal S, Jaakson K, Baiget M, Navarro R, Ayuso C. Valverde D, et al. Among authors: baiget m. Mol Vis. 2006 Aug 11;12:902-8. Mol Vis. 2006. PMID: 16917483 Free article.

4

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. Among authors: baiget m. 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

5

Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.

Gamundi MJ, Hernan I, Maseras M, Baiget M, Ayuso C, Borrego S, Antiñolo G, Millán JM, Valverde D, Carballo M. Gamundi MJ, et al. Among authors: baiget m. Mol Vis. 2005 Nov 2;11:922-8. Mol Vis. 2005. PMID: 16280978 Free article.

6

Spectrum of the ABCA4 gene mutations implicated in severe retinopathies in Spanish patients.

Valverde D, Riveiro-Alvarez R, Aguirre-Lamban J, Baiget M, Carballo M, Antiñolo G, Millán JM, Garcia Sandoval B, Ayuso C. Valverde D, et al. Among authors: baiget m. Invest Ophthalmol Vis Sci. 2007 Mar;48(3):985-90. doi: 10.1167/iovs.06-0307. Invest Ophthalmol Vis Sci. 2007. PMID: 17325136

7

High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population.

Gamundi MJ, Hernan I, Muntanyola M, Trujillo MJ, García-Sandoval B, Ayuso C, Baiget M, Carballo M. Gamundi MJ, et al. Among authors: baiget m. Mol Vis. 2007 Jun 28;13:1031-7. Mol Vis. 2007. PMID: 17653047 Free PMC article.

8

Complexity of phenotype-genotype correlations in Spanish patients with RDH12 mutations.

Valverde D, Pereiro I, Vallespín E, Ayuso C, Borrego S, Baiget M. Valverde D, et al. Among authors: baiget m. Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1065-8. doi: 10.1167/iovs.08-2083. Epub 2008 Nov 14. Invest Ophthalmol Vis Sci. 2009. PMID: 19011012

9

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: baiget m. 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.

10

Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.

Barragán I, Borrego S, Pieras JI, González-del Pozo M, Santoyo J, Ayuso C, Baiget M, Millan JM, Mena M, Abd El-Aziz MM, Audo I, Zeitz C, Littink KW, Dopazo J, Bhattacharya SS, Antiñolo G. Barragán I, et al. Among authors: baiget m. Hum Mutat. 2010 Nov;31(11):E1772-800. doi: 10.1002/humu.21334. Hum Mutat. 2010. PMID: 21069908 Free PMC article.

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