Miguel Carballo
Overview
Explore the profile of Miguel Carballo including associated specialties, affiliations and a list of published articles.
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Articles
33
Citations
468
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Recent Articles
1.
Milla E, Laguna J, Alforja M, Pascual B, Gamundi M, Borras E, et al.
PLoS One
. 2024 Jan;
19(1):e0282133.
PMID: 38241218
Primary open-angle glaucoma (POAG) is a complex disease with a strong hereditably component. Several genetic variants have recently been associated with POAG, partially due to technological improvements such as next-generation...
2.
Biarnes M, Ferraro L, Hernan I, Gamundi M, Garcia Planas M, Abadias C, et al.
Clin Exp Optom
. 2023 Jun;
107(6):679-682.
PMID: 37349105
No abstract available.
3.
Arzalluz-Luque A, Cabrera J, Skottman H, Benguria A, Bolinches-Amoros A, Cuenca N, et al.
Front Neurosci
. 2021 May;
15:636969.
PMID: 33994920
Retinitis pigmentosa (RP) is a rare, progressive disease that affects photoreceptors and retinal pigment epithelial (RPE) cells with blindness as a final outcome. Despite high medical and social impact, there...
4.
Martin-Merida I, Aguilera-Garcia D, Fernandez-San J, Blanco-Kelly F, Zurita O, Almoguera B, et al.
Invest Ophthalmol Vis Sci
. 2018 May;
59(6):2345-2354.
PMID: 29847639
Purpose: To provide a comprehensive overview of the molecular basis of autosomal dominant retinitis pigmentosa (adRP) in Spanish families. Thus, we established the molecular characterization rate, gene prevalence, and mutational...
5.
Milla E, Gamundi M, Duch S, Rios J, Carballo M, Study Group E
J Ophthalmol
. 2017 Oct;
2017:1907454.
PMID: 29082038
Introduction: The aim of the study was to make a phenotypic description of the Spanish multicentre glaucoma group cohort of patients. Design: Retrospective, observational, multicentre, cohort study. Material And Methods:...
6.
Lukovic D, Bolinches-Amoros A, Artero-Castro A, Pascual B, Carballo M, Hernan I, et al.
Stem Cell Res
. 2017 Jul;
21:23-25.
PMID: 28677533
The human iPSC cell line, RP2-FiPS4F1 (RCPFi001-A), derived from dermal fibroblasts from the patient with retinitis pigmentosa caused by the mutation of the gene PRPF8, was generated by non-integrative reprogramming...
7.
Martin-Merida I, Sanchez-Alcudia R, Fernandez-San Jose P, Blanco-Kelly F, Perez-Carro R, Rodriguez-Jacy da Silva L, et al.
Invest Ophthalmol Vis Sci
. 2017 Feb;
58(2):1045-1053.
PMID: 28192796
Purpose: The aim was to determine the prevalence of PRPF31 mutations in a cohort of Spanish autosomal dominant retinitis pigmentosa (adRP) families to deepen knowledge of the pathogenic mechanisms underlying...
8.
Mateos-Munoz B, Garcia-Martin E, Torrejon M, Devesa-Medina M, Esguevillas G, Cardenas M, et al.
Medicine (Baltimore)
. 2016 Mar;
95(10):e3019.
PMID: 26962819
Insulin resistance (IR) is found in chronic hepatitis C (CHC) more frequently than in other chronic liver diseases.Prospective cross-sectional study to evaluate a wide multitest panel to identify factors related...
9.
de Sousa Dias M, Hernan I, Delas B, Pascual B, Borras E, Gamundi M, et al.
Mol Vis
. 2015 Sep;
21:857-70.
PMID: 26321861
Purpose: This study aimed to test a newly devised cost-effective multiplex PCR assay for the molecular diagnosis of autosomal dominant retinitis pigmentosa (adRP), as well as the use of whole-exome...
10.
Fernandez-San Jose P, Blanco-Kelly F, Corton M, Trujillo-Tiebas M, Gimenez A, Avila-Fernandez A, et al.
Acta Ophthalmol
. 2014 Nov;
93(1):e38-44.
PMID: 25408095
Purpose: We aimed to determine the prevalence of mutations in the RHO gene in Spanish families with autosomal dominant Retinitis Pigmentosa (adRP), to assess genotype-phenotype correlations and to establish an...