Milla E - Search Results

1

Phenotypic Description of the Spanish Multicentre Genetic Glaucoma Group Cohort.

Milla E, Gamundi MJ, Duch S, Rios J, Carballo M, Study Group E. Milla E, et al. J Ophthalmol. 2017;2017:1907454. doi: 10.1155/2017/1907454. Epub 2017 Sep 26. J Ophthalmol. 2017. PMID: 29082038 Free PMC article.

2

[Genetic and molecular characterization of 148 patients with autosomal dominant retinitis pigmentosa (ADRP)].

Millá E, Maseras M, Martínez-Gimeno M, Gamundi MJ, Assaf H, Esmerado C, Carballo M; Grupo Multicéntrico Español de Retinosis Pigmentaria. Millá E, et al. Arch Soc Esp Oftalmol. 2002 Sep;77(9):481-4. Arch Soc Esp Oftalmol. 2002. PMID: 12221539 Spanish.

3

Mutations in the pre-mRNA splicing-factor genes PRPF3, PRPF8, and PRPF31 in Spanish families with autosomal dominant retinitis pigmentosa.

Martínez-Gimeno M, Gamundi MJ, Hernan I, Maseras M, Millá E, Ayuso C, García-Sandoval B, Beneyto M, Vilela C, Baiget M, Antiñolo G, Carballo M. Martínez-Gimeno M, et al. Among authors: milla e. Invest Ophthalmol Vis Sci. 2003 May;44(5):2171-7. doi: 10.1167/iovs.02-0871. Invest Ophthalmol Vis Sci. 2003. PMID: 12714658

4

Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma.

Millá E, Hernan I, Gamundi MJ, Martínez-Gimeno M, Carballo M. Millá E, et al. Mol Vis. 2007 Apr 27;13:639-48. Mol Vis. 2007. PMID: 17515884 Free PMC article.

5

Poor agreement between Goldmann and Pascal tonometry in eyes with extreme pachymetry.

Milla E, Duch S, Buchacra O, Masuet C. Milla E, et al. Eye (Lond). 2009 Mar;23(3):536-42. doi: 10.1038/eye.2008.90. Epub 2008 Mar 28. Eye (Lond). 2009. PMID: 18369376 Clinical Trial.

6

Intracameral bevacizumab (Avastin) for neovascular glaucoma: a pilot study in 6 patients.

Duch S, Buchacra O, Milla E, Andreu D, Tellez J. Duch S, et al. Among authors: milla e. J Glaucoma. 2009 Feb;18(2):140-3. doi: 10.1097/IJG.0b013e318170a747. J Glaucoma. 2009. PMID: 19225351

7

One-year analysis of the iStent trabecular microbypass in secondary glaucoma.

Buchacra O, Duch S, Milla E, Stirbu O. Buchacra O, et al. Among authors: milla e. Clin Ophthalmol. 2011;5:321-6. doi: 10.2147/OPTH.S15025. Epub 2011 Mar 4. Clin Ophthalmol. 2011. PMID: 21468340 Free PMC article.

8

Novel FBN1 mutation causes Marfan syndrome with bilateral ectopia lentis and refractory glaucoma.

Milla E, Leszczynska A, Rey A, Navarro M, Larena C. Milla E, et al. Eur J Ophthalmol. 2012 Jul-Aug;22(4):667-9. doi: 10.5301/ejo.5000070. Eur J Ophthalmol. 2012. PMID: 22034023

9

Spanish multicenter tafluprost tolerability study.

Milla E, Stirbu O, Rey A, Duch S, Buchacra O, Robles A, Navarro C, Gil R, Cordero JM. Milla E, et al. Br J Ophthalmol. 2012 Jun;96(6):826-31. doi: 10.1136/bjophthalmol-2011-301015. Epub 2012 Mar 7. Br J Ophthalmol. 2012. PMID: 22399693 Clinical Trial.

10

Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.

Millá E, Mañé B, Duch S, Hernan I, Borràs E, Planas E, Dias Mde S, Carballo M, Gamundi MJ; Spanish Multicenter Glaucoma Group-Estudio Multicéntrico Español de Investigación Genética del Glaucoma, EMEIGG. Millá E, et al. Mol Vis. 2013 Aug 4;19:1707-22. Print 2013. Mol Vis. 2013. PMID: 23922489 Free PMC article.

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