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Search Results - Cabral-Macías, Jesús
Search Results - Cabral-Macías, Jesús
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Adjuntive nicergoline therapy for severe persistent corneal epithelial defects
by
Oliva-Biénzobas, Valeria
,
Graue-Hernandez, Enrique O.
,
Vera-Duarte, Guillermo Raul
,
Cabral-Macías, Jesus
,
Serna-Ojeda, Juan
,
Boullosa, Victor
,
Ramirez-Miranda, Arturo
,
Jhanji, Vishal
,
Perez, Victor L.
,
Navas, Alejandro
Published in
AJO International
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Association study of multiple gene polymorphisms with the risk of adult-onset primary open-angle glaucoma in a Mexican population
by
Buentello-Volante, Beatriz
,
Elizondo-Olascoaga, Celia
,
Miranda-Duarte, Antonio
,
Guadarrama-Vallejo, Dalia
,
Cabral-Macias, Jesús
,
Zenteno, Juan C.
Published in
Experimental eye research
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Aplasia Cutis Congenita of the Scalp in a Female Infant With Anophthalmia/Microphthalmia-Esophageal Atresia Syndrome Negative for SOX2 Mutation
by
Corona-Rivera, J. Román
,
Zenteno, Juan Carlos
,
Pelcastre-Luna, Erika
,
Miguel-Jiménez, Karla
,
Aguirre-Guillén, Rafael L.
,
Cabral-Macías, Jesús
,
Peña-Padilla, Christian
,
Bobadilla-Morales, Lucina
,
Corona-Rivera, Alfredo
Published in
American journal of medical genetics. Part A
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Combined Bacterial and Herpes Simplex Virus Keratitis following Small-Incision Lenticule Extraction for the Correction of Myopia
by
Ramirez-Miranda, Arturo
,
Mangwani-Mordani, Simran
,
Quiroz-Casian, Natalia
,
Oliva-Bienzobas, Valeria
,
Cabral-Macias, Jesus
,
Navas, Alejandro
,
Graue-Hernandez, Enrique O.
Published in
Case reports in ophthalmology
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Aplasia Cutis Congenita of the Scalp in a Female Infant With Anophthalmia/ M icrophthalmia– E sophageal Atresia Syndrome Negative for SOX 2 Mutation
by
Corona‐Rivera, J. Román
,
Zenteno, Juan Carlos
,
Pelcastre‐Luna, Erika
,
Miguel‐Jiménez, Karla
,
Aguirre‐Guillén, Rafael L.
,
Cabral‐Macías, Jesús
,
Peña‐Padilla, Christian
,
Bobadilla‐Morales, Lucina
,
Corona‐Rivera, Alfredo
Published in
American journal of medical genetics. Part A
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Doble lentículo como complicación de SMILE
by
Navas, Alejandro
,
Graue-Hernández, Enrique O.
,
Ramírez-Miranda, Arturo
,
Cabral-Macias, Jesús
Published in
Revista mexicana de oftalmología
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Clinical, histopathological, and in silico pathogenicity analyses in a pedigree with familial amyloidosis of the Finnish type (Meretoja syndrome) caused by a novel gelsolin mutatio...
by
Cabral-Macias, Jesus
,
Garcia-Montaño, Leopoldo A
,
Pérezpeña-Díazconti, Mario
,
Aguilar, Marisa-Cruz
,
Garcia, Guillermo
,
Vencedor-Meraz, Carlos I
,
Graue-Hernandez, Enrique O
,
Chacón-Camacho, Oscar F
,
Zenteno, Juan C
Published in
Molecular vision
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Rhodopsin p.N78I dominant mutation causing sectorial retinitis pigmentosa in a pedigree with intrafamilial clinical heterogeneity
by
Rivera-De la Parra, David
,
Cabral-Macias, Jesus
,
Matias-Florentino, Margarita
,
Rodriguez-Ruiz, Gabriela
,
Robredo, Violeta
,
Zenteno, Juan Carlos
Published in
Gene
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Update on the Surgical Reconstruction of Ocular Surface in Eyes with Limbal Stem Cell Deficiency
by
Cabral-Macias, Jesus
,
Martinez, Jaime D.
,
Naranjo, Andrea
,
Amescua, Guillermo
Published in
Current ophthalmology reports
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Combined Bacterial and Herpes Simplex Virus Keratitis following Small-Incision Lenticule Extraction for the Correction of Myopia
by
Ramirez-Miranda, Arturo
,
Mangwani-Mordani, Simran
,
Quiroz-Casian, Natalia
,
Oliva-Bienzobas, Valeria
,
Cabral-Macias, Jesus
,
Navas, Alejandro
,
Graue-Hernandez, Enrique O
Published in
Case reports in ophthalmology
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