Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Angel Nava-Castañeda"'
Publikováno v:
Nepalese journal of ophthalmology : a biannual peer-reviewed academic journal of the Nepal Ophthalmic Society : NEPJOPH. 13(24)
Introduction: Functional and anatomical success after canalicular laceration repair using only Crawford bicanalicular stents was evaluated in a ophthalmological teaching center. The objective of this study was to evaluate functional and anatomical su
Autor:
Mario Perezpeña-Diazconti, Thania Ordaz-Robles, Juan Carlos Zenteno, Rocio Arce-Gonzalez, Angel Nava-Castañeda, Oscar F. Chacon-Camacho
Publikováno v:
American Journal of Medical Genetics Part A. 182:2773-2777
Hereditary mucoepithelial dysplasia (HMD) is an uncommon autosomal dominant disease affecting skin, mucosae, hair, eyes, and lungs. Prominent clinical features include non-scarring alopecia, mucosal erythema, perineal erythematous intertrigo, and inv
Autor:
Nicolás Kahuam-López, Abelardo A. Rodríguez-Reyes, Yesica De La Fuente Díez, Lilia Garnica-Hayashi, Fernando Ariel Martin, Angel Nava-Castañeda, Adriana Velásco Y Levy, Franchesca Ginette Sánchez-Bonilla
Publikováno v:
Orbit (Amsterdam, Netherlands). 40(6)
Adenoid cystic carcinoma (ACC) is a slow-growing, locally invasive tumor of epithelial origin. The common sites of origin are the minor and major salivary glands and also the lacrimal glands. ACC accounts for 4.8% of primary orbital neoplasms and com
Autor:
Osiris Olvera-Morales, Angel Nava-Castañeda, Adriana Davila-Camargo, Jose-Luis Tovilla-Canales, Lourdes Rodríguez-Cabrera, Sharon Ball-Burstein
Publikováno v:
Orbit (Amsterdam, Netherlands). 39(5)
To present the clinical picture and radiological characteristics of orbital manifestations of granulomatosis with polyangiitis in a Mexican hospital and compare them with worldwide literature.Retrospective, observational study from January 2007 to Ja
Publikováno v:
Orbit. 38:383-386
Purpose: To describe and evaluate the eyelash transplantation with strip composite eyebrow graft to improve eyelid anatomy in tarsoconjunctival flap eyelid reconstruction procedure.Methods:...
Autor:
Angel Nava-Castañeda, Lourdes Rodríguez-Cabrera, Francisca Zuazo, Lilia Garnica-Hayashi, José Luis Tovilla-Canales
Publikováno v:
Nepalese Journal of Ophthalmology. 9:70-73
Background: Alveolar Soft Part Sarcoma is a rare malignant tumor of uncertain histogenesis, representing 0.5-1% of all soft tissue tumors. It occurs predominantly in head and neck regions, especially the orbit and the tongue, in infants, causing no s
Autor:
Angel Nava-Castañeda, Marisa Cruz-Aguilar, Caroline Guerrero-de Ferran, Juan Carlos Zenteno, José Luis Tovilla-Canales
Publikováno v:
Journal of Investigative Medicine. 65:705-708
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal-dominant, adult-onset disorder defined by blepharoptosis, dysphagia, and proximal muscle weakness. OPMD arises from heterozygous expansions of a trinucleotide (GCN) tract situated at the 5′
Autor:
Genaro Rodríguez-Uribe, Angel Nava-Castañeda, Ana María Borbolla, Acatzin Salgado-Medina, Tania Barragán-Arévalo, Nayeli Alcaraz-Lares, Esther Lieberman, Lourdes Rodríguez-Cabrera, Liliana Fernández-Hernández, Oscar F. Chacon-Camacho, Daniel López-Moreno, Enrique O Graue-Hernandez, Ariadna González-del Angel, Juan Carlos Zenteno
Publikováno v:
Gene. 706
Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) is an autosomal dominant entity characterized by eyelid malformations and caused by mutations in the forkhead box L2 (FOXL2) gene. Clinical and genetic analyses of large cohorts of BPES pati
Autor:
Cynthia Ramos-Castellon, Lilia Garnica-Hayashi, Yonathan Garfias, Osiris Olvera-Morales, Angel Nava-Castañeda
Publikováno v:
Clinical & Experimental Ophthalmology. 42:235-241
Background To investigate the efficacy and safety of subconjunctival bevacizumab application as an adjuvant therapy for primary pterygium. Design This study was a clinical randomized trial performed at the Institute of Ophthalmology ‘Conde de Valen
Autor:
Marisa, Cruz-Aguilar, Caroline, Guerrero-de Ferran, Jose Luis, Tovilla-Canales, Angel, Nava-Castañeda, Juan C, Zenteno
Publikováno v:
Journal of investigative medicine : the official publication of the American Federation for Clinical Research. 65(3)
Oculopharyngeal muscular dystrophy (OPMD) is an autosomal-dominant, adult-onset disorder defined by blepharoptosis, dysphagia, and proximal muscle weakness. OPMD arises from heterozygous expansions of a trinucleotide (GCN) tract situated at the 5' re