Review and update on the molecular basis of Leber congenital amaurosis

Por Chacon-Camacho, Oscar Francisco, Zenteno, Juan Carlos
Publicado no World J Clin Cases (2015)

The T allele of lysyl oxidase-like 1 rs41435250 is a novel risk factor for pseudoexfoliation syndrome and pseudoexfoliation glaucoma independently and through intragenic epistatic...

Por Guadarrama-Vallejo, Dalia, Miranda-Duarte, Antonio, Zenteno, Juan Carlos
Publicado em 2013

Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations

Por Zenteno, Juan Carlos, Ruiz, Gabriela, Pérez-Cano, Hector J., Camargo, Mayra
Publicado em 2008

Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex

Por Zenteno, Juan Carlos, Buentello-Volante, Beatriz, Quiroz-González, Miguel A., Quiroz-Reyes, Miguel A.
Publicado em 2009

Cerebral hemihypoplasia and nevus flammeus in a child with oromandibular limb hypogenesis syndrome type III

Por Toral-López, Jaime, Córdoba-Cabeza, Tania, Villeda, Maricela, Cortes-Castillo, Gabriel, Zenteno, Juan Carlos
Publicado no J Pediatr Genet (2013)

Comparative expression analysis of aquaporin-5 (AQP5) in keratoconic and healthy corneas

Por Garfias, Yonathan, Navas, Alejandro, Pérez-Cano, Hector J., Quevedo, Jonathan, Villalvazo, Leonardo, Zenteno, Juan Carlos
Publicado em 2008

Clinical and Genetic Characteristics of Mexican Patients with Juvenile Presentation of Niemann-Pick Type C Disease

Por Piña-Aguilar, Raul E., Vera-Loaiza, Aurea, Chacón-Camacho, Oscar F., Zenteno, Juan Carlos, Nuñez-Orozco, Lilia, Santillán-Hernández, Yuritzi
Publicado em 2014

CFH haplotypes and ARMS2, C2, C3, and CFB alleles show association with susceptibility to age-related macular degeneration in Mexicans

Por Contreras, Alejandra V., Zenteno, Juan Carlos, Fernández-López, Juan Carlos, Rodríguez-Corona, Ulises, Falfán-Valencia, Ramcés, Sebastian, Leticia, Morales, Fabiola, Ochoa-Contreras, Daniel, Carnevale, Alessandra, Silva-Zolezzi, Irma
Publicado em 2014

Congenital Hereditary Endothelial Dystrophy Caused by SLC4A11 Mutations Progresses to Harboyan Syndrome

Por Siddiqui, Salina, Zenteno, Juan Carlos, Rice, Aine, Chacón-Camacho, Oscar, Naylor, Steven G., Rivera-de la Parra, David, Spokes, David M., James, Nigel, Toomes, Carmel, Inglehearn, Chris F., Ali, Manir
Publicado em 2013

Vortex pattern of corneal deposits in granular corneal dystrophy associated with the p. (ArgR555WTrp) mutation in TGFBI

Por Kattan, Jaffer M., Serna-Ojeda, Juan Carlos, Sharma, Anushree, Kim, Eung K., Ramirez-Miranda, Arturo, Cruz-Aguilar, Marisa, Cervantes, Aleck E., Frausto, Ricardo F., Zenteno, Juan Carlos, Graue-Hernandez, Enrique O., Aldave, Anthony J.
Publicado no Cornea (2017)

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma

Por Ali, Manir, Buentello-Volante, Beatriz, McKibbin, Martin, Rocha-Medina, J. Alberto, Fernandez-Fuentes, Narcis, Koga-Nakamura, Wilson, Ashiq, Aruna, Khan, Kamron, Booth, Adam P., Williams, Grange, Raashid, Yasmin, Jafri, Hussain, Rice, Aine, Inglehearn, Chris F., Zenteno, Juan Carlos
Publicado em 2010