Zobrazeno 1 - 10
of 19
pro vyhledávání: '"José Luis Tovilla-Canales"'
Publikováno v:
Journal of Ophthalmology, Vol 2013 (2013)
Objective. To compare 18-fluorodeoxyglucose (FDG) uptake by positron emission tomography (PET) in extraocular muscles (EOMs) of patients with Graves’ ophthalmopathy (GO) versus patients without GO. Design. Prospective, observational, comparative, a
Externí odkaz:
https://doaj.org/article/c0c6495192124677b4d4544cb1cc3854
Akademický článek
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Publikováno v:
The Pan-American Journal of Ophthalmology, Vol 2, Iss 1, Pp 32-32 (2020)
We present a case of an orbital mass confirmed as Castleman disease (CD) with the histopathological and immunohistochemical review. CD in the orbit is uncommon and has been seldom reported. The case we present justifies the review due to the abnormal
Externí odkaz:
https://doaj.org/article/44200ef4157f47d396088319a704dfab
Publikováno v:
Revista Mexicana de Oftalmología. 95
Publikováno v:
Revista Mexicana de Oftalmología (English Edition). 95
Autor:
Adam Weber, Mica Y Bergman, Juan C. Jiménez-Pérez, J. Javier Servat, Shu Hong Chang, Michael E. Migliori, Catherine Y. Liu, Victoria Starks, Catherine J. Choi, Bradford W. Lee, N. Grace Lee, Osiris Olvera-Morales, Livia Teo, Chau Pham, Liza M. Cohen, Nicholas R. Mahoney, Michael K. Yoon, Peter W. MacIntosh, Joseph Giacometti, Arpine Barsegian, Christina H. Choe, Senmiao Zhan, Omar Dajani, Anne Barmettler, Sonul Mehta, Ashley A. Campbell, Vinay K. Aakalu, Lucas Bonafede, Jeremiah P. Tao, Ann Q. Tran, Suzanne K. Freitag, Sanjai Jalaj, Julius T. Oatts, Roxana Fu, Shu Lang Liao, Lora R. Dagi Glass, Ian F. Dunn, Blair K. Armstrong, Mithra O. Gonzalez, Pete Setabutr, Honglei Liu, Michael T. Yen, Natalie Homer, José Luis Tovilla-Canales, Roman Shinder, Brittany A. Simmons, Alexandra T. Elliott, Seanna Grob, Kian Eftekhari, Edward J. Wladis, Prashant Yadav, Bryan J. Winn, Do Eon Rok, Gary J. Lelli, Sandy Zhang-Nunes, Wenya Linda Bi, Benjamin S. Bleier, Jason S. Mantagos, Larissa H. Habib, Natalie Wolkow, Hunter Yuen, Neil Shah, Kristen E. Dunbar, Michael Tseng, Emily Charlson, Christopher B. Chambers, Alison B. Callahan, Sarina K. Mueller, Nora K. Siegal, Daniel R. Lefebvre, Kyle J. Godfrey, Tieu Vy Nguyen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e301d148267b38565f9f9bd42bc5de27
https://doi.org/10.1055/b-006-163725
https://doi.org/10.1055/b-006-163725
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:
Juan Carlos Zenteno, Francisca Zuazo, Patricia Garcia-Regil, Lourdes Rodríguez-Cabrera, Mirena C Astiazarán, José Luis Tovilla-Canales, Oscar F. Chacon-Camacho
Publikováno v:
Ophthalmic Plastic & Reconstructive Surgery. 34:e61-e63
Barber-Say syndrome is a rare autosomal dominant disease characterized by dysmorphic features, mainly of the eyelids and skin. It is caused by heterozygous mutations in gene TWIST2, localized in chromosome 2q37.3. The authors present the case of a pe