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SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa.
Published in:
Ophthalmic Genetics, 2016, v. 37, n. 3, p. 333, doi. 10.3109/13816810.2015.1130154
By:
- Matsui, Rodrigo;
- McGuigan III, David B.;
- Gruzensky, Michaela L.;
- Aleman, Tomas S.;
- Schwartz, Sharon B.;
- Sumaroka, Alexander;
- Koenekoop, Robert K.;
- Cideciyan, Artur V.;
- Jacobson, Samuel G.
Publication type:
Article
Multimodal imaging and genetic screening in Mexican patients with Gyrate atrophy: identification of novel OAT pathogenic variants.
Published in:
International Ophthalmology, 2024, v. 45, n. 1, p. 1, doi. 10.1007/s10792-024-03260-0
By:
- Díazceballos-García, Ana Lía;
- Matsui, Rodrigo;
- Chairez Miranda, María Graciela;
- Rosales Padrón, Jaime Francisco;
- Graue-Wiechers, Federico;
- Zenteno, Juan Carlos
Publication type:
Article
Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast.
Published in:
BMC Ophthalmology, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12886-015-0085-0
By:
- Roman, Alejandro J.;
- Cideciyan, Artur V.;
- Matsui, Rodrigo;
- Sheplock, Rebecca;
- Schwartz, Sharon B.;
- Jacobson, Samuel G.
Publication type:
Article
Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrast.
Published in:
BMC Ophthalmology, 2015, v. 15, n. 1, p. 98, doi. 10.1186/s12886-015-0085-0
By:
- Roman, Alejandro J.;
- Cideciyan, Artur V.;
- Matsui, Rodrigo;
- Sheplock, Rebecca;
- Schwartz, Sharon B.;
- Jacobson, Samuel G.
Publication type:
Article
Clinical-genetic findings in a group of subjects with macular dystrophies due to mutations in rare inherited retinopathy genes.
Published in:
Graefe's Archive of Clinical & Experimental Ophthalmology, 2023, v. 261, n. 2, p. 353, doi. 10.1007/s00417-022-05786-4
By:
- Zenteno, Juan C.;
- Arce-Gonzalez, Rocio;
- Matsui, Rodrigo;
- Lopez-Bolaños, Antonio;
- Montes, Luis;
- Martinez-Aguilar, Alan;
- Chacon-Camacho, Oscar F.
Publication type:
Article
Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next‐generation sequencing.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 1, p. N.PAG, doi. 10.1002/mgg3.1044
By:
- Zenteno, Juan C.;
- García‐Montaño, Leopoldo A.;
- Cruz‐Aguilar, Marisa;
- Ronquillo, Josué;
- Rodas‐Serrano, Agustín;
- Aguilar‐Castul, Luis;
- Matsui, Rodrigo;
- Vencedor‐Meraz, Carlos I.;
- Arce‐González, Rocío;
- Graue‐Wiechers, Federico;
- Gutiérrez‐Paz, Mario;
- Urrea‐Victoria, Tatiana;
- Dios Cuadras, Ulises;
- Chacón‐Camacho, Oscar F.
Publication type:
Article
Pediatric rhegmatogenous retinal detachment: predictors of anatomic and functional success.
Published in:
International Ophthalmology, 2021, v. 41, n. 8, p. 2777, doi. 10.1007/s10792-021-01834-w
By:
- Carranza-Casas, Mario;
- Quiroz-González, Erick;
- Hernández-Reyes, Alejandro;
- Matsui-Serrano, Rodrigo;
- Ariza-Camacho, Enrique;
- Graue-Wiechers, Federico
Publication type:
Article
Retinal phenotypic characterization of patients with ABCA4 retinopathy due to the homozygous p.Ala1773Val mutation.
Published in:
Molecular Vision, 2018, v. 24, p. 105
By:
- López-Rubio, Salvador;
- Chacon-Camacho, Oscar F.;
- Matsui, Rodrigo;
- Guadarrama-Vallejo, Dalia;
- Astiazarán, Mirena C.;
- Zenteno, Juan C.
Publication type:
Article

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