Výsledky vyhledávání

Analysis of penetrating keratoplasty in Northern Alberta, Canada, from 2000 to 2015

Autor: Khaliq H. Kurji, Calvin Tseng, Matthew D. Benson, Bo Bao, Dean Mah

Publikováno v: Canadian Journal of Ophthalmology. 53:568-573

Objective To study indications for penetrating keratoplasty (PK) at a single site. The trends in the causative organisms for infectious keratitis requiring surgery were also evaluated. Design Retrospective observational study. Participants A total of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e4fa77e69995faf78f945ea32449129
https://doi.org/10.1016/j.jcjo.2018.01.024

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Trabecular Micro-Bypass Stent Use in Necrotizing Scleritis

Autor: Simrenjeet Sandhu, Lisa Heckler, Dean Mah, Michael W. Dorey

Publikováno v: Journal of glaucoma. 26(2)

PURPOSE In this case report, we describe the successful implantation of multiple trabecular micro-bypass iStents in a patient with necrotizing scleritis. DESIGN The study design is a case report. PARTICIPANTS The participant was a patient who underwe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b30feaf94c259462ec263a339aed74e
https://pubmed.ncbi.nlm.nih.gov/27977475

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Focal limbal stem cell deficiency in Turner syndrome: report of two patients and review of the literature

Autor: M. Hermina Strungaru, Clara C. Chan, Dean Mah

Publikováno v: Cornea. 33(2)

Purpose The aim of this study was to report the presence of focal limbal stem cell deficiency (LSCD) in 2 cases of Turner syndrome. Methods This is a case review. Results A 25-year-old woman with a history of Turner syndrome diagnosed at 15 years of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4b919457bdbd6b135c6925281276ff0
https://pubmed.ncbi.nlm.nih.gov/24342891

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Choroideremia gene testing

Autor: Ian M. MacDonald, Christina Sereda, Kerry E. McTaggart, Dean Mah

Publikováno v: Expert review of molecular diagnostics. 4(4)

Choroideremia is a chorioretinal degeneration displaying X-linked recessive inheritance. In recent years, technological advances have increased the accessibility of genetic testing for mutations in the gene that lead to this disorder. The disorder it

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92714de921dab9ecd488a64ab43e9ffc
https://pubmed.ncbi.nlm.nih.gov/15225095

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