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Federico Graue-Wiechers

Showing results (1-10 of 21) with videos related to

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Current Eye Research|April 10, 2008
Novel CYP4V2 gene mutation in a Mexican patient with Bietti's crystalline corneoretinal dystrophyJuan C Zenteno, Raul Ayala-Ramirez, Federico Graue-Wiechers
Current Eye Research|December 5, 2009
Molecular screening of rhodopsin and peripherin/RDS genes in Mexican families with autosomal dominant retinitis pigmentosaMargarita Matias-Florentino, Raul Ayala-Ramirez, Federico Graue-Wiechers, et al.
Case Reports in Ophthalmology|May 23, 2012
Presumed idiopathic central serous chorioretinopathy in a 12-year-old girlJuan P Velazquez-Martin, Emiliano Fulda, Daniela Domville, et al.
International Medical Case Reports Journal|December 4, 2020
Partial Central Retinal Artery Occlusion: An Underrecognized EntityMario Carranza-Casas, Jorge E Aceves-Velazquez, René Cano-Hidalgo, et al.
American Journal of Ophthalmology Case Reports|August 20, 2024
Delayed manifestation of proliferative retinopathy associated with chronic myeloid leukemiaAlan Chew Bonilla, Paulina Bueno Zarazúa, Jaime Rosales Padron, et al.
Molecular Vision|December 15, 2006
A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutationRaul Ayala-Ramirez, Federico Graue-Wiechers, Violeta Robredo, et al.
International Ophthalmology|April 11, 2021
Pediatric rhegmatogenous retinal detachment: predictors of anatomic and functional successMario Carranza-Casas, Erick Quiroz-González, Alejandro Hernández-Reyes, et al.
Ophthalmic Genetics|March 5, 2025
<i>ABCC6</i> gene mutational spectrum and ocular features in Mexican patients with pseudoxanthoma elasticum-related angioid streaksJaime Rosales-Padron, Oscar F Chacon-Camacho, Vianey Ordoñez-Labastida, et al.
International Ophthalmology|December 7, 2024
Multimodal imaging and genetic screening in Mexican patients with Gyrate atrophy: identification of novel OAT pathogenic variantsAna Lía Díazceballos-García, Rodrigo Matsui, María Graciela Chairez Miranda, et al.
Cureus|May 22, 2026
Prevalence of Branch Retinal Vein Occlusion in the Latin Population: Insights Into Clinical EpidemiologyMario Leon Meza, Braulio Hernán Velasco-Sepúlveda, Jorge Gerardo Morales Navarro, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Current Eye Research|April 10, 2008
Novel CYP4V2 gene mutation in a Mexican patient with Bietti's crystalline corneoretinal dystrophyJuan C Zenteno, Raul Ayala-Ramirez, Federico Graue-Wiechers
Current Eye Research|December 5, 2009
Molecular screening of rhodopsin and peripherin/RDS genes in Mexican families with autosomal dominant retinitis pigmentosaMargarita Matias-Florentino, Raul Ayala-Ramirez, Federico Graue-Wiechers, et al.
Case Reports in Ophthalmology|May 23, 2012
Presumed idiopathic central serous chorioretinopathy in a 12-year-old girlJuan P Velazquez-Martin, Emiliano Fulda, Daniela Domville, et al.
International Medical Case Reports Journal|December 4, 2020
Partial Central Retinal Artery Occlusion: An Underrecognized EntityMario Carranza-Casas, Jorge E Aceves-Velazquez, René Cano-Hidalgo, et al.
American Journal of Ophthalmology Case Reports|August 20, 2024
Delayed manifestation of proliferative retinopathy associated with chronic myeloid leukemiaAlan Chew Bonilla, Paulina Bueno Zarazúa, Jaime Rosales Padron, et al.
Molecular Vision|December 15, 2006
A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutationRaul Ayala-Ramirez, Federico Graue-Wiechers, Violeta Robredo, et al.
International Ophthalmology|April 11, 2021
Pediatric rhegmatogenous retinal detachment: predictors of anatomic and functional successMario Carranza-Casas, Erick Quiroz-González, Alejandro Hernández-Reyes, et al.
Ophthalmic Genetics|March 5, 2025
<i>ABCC6</i> gene mutational spectrum and ocular features in Mexican patients with pseudoxanthoma elasticum-related angioid streaksJaime Rosales-Padron, Oscar F Chacon-Camacho, Vianey Ordoñez-Labastida, et al.
International Ophthalmology|December 7, 2024
Multimodal imaging and genetic screening in Mexican patients with Gyrate atrophy: identification of novel OAT pathogenic variantsAna Lía Díazceballos-García, Rodrigo Matsui, María Graciela Chairez Miranda, et al.
Cureus|May 22, 2026
Prevalence of Branch Retinal Vein Occlusion in the Latin Population: Insights Into Clinical EpidemiologyMario Leon Meza, Braulio Hernán Velasco-Sepúlveda, Jorge Gerardo Morales Navarro, et al.
Pageof 3