Date: 2020 / Author/Creator: Fan, Kenneth C. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Date 2020 Author/Creator Fan, Kenneth C.

1. A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations. (3rd July 2020)

Authors:: Han, Elaine; Patel, Nimesh A.; Yannuzzi, Nicolas A.; Laura, Diana M.; Fan, Kenneth C.; Negron, Catherin I.; Prakhunhungsit, Supalert; Thorson, Willa L.; Berrocal, Audina M.
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 4(2020)
Page Start:: 363
Record Type:: Journal Article
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2. A unique case of coats plus syndrome and dyskeratosis congenita in a patient with CTC1 mutations. (3rd July 2020)

Authors:: Han, Elaine; Patel, Nimesh A.; Yannuzzi, Nicolas A.; Laura, Diana M.; Fan, Kenneth C.; Negron, Catherin I.; Prakhunhungsit, Supalert; Thorson, Willa L.; Berrocal, Audina M.
Journal:: Ophthalmic genetics
Issue:: Volume 41:Number 4(2020)
Page Start:: 363
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. The Perioperative Management of Giant Retinal Tears. Issue 3 (2020)

Authors:: Fan, Jason; Lin, James; Fan, Kenneth C.; Sridhar, Jayanth
Journal:: International ophthalmology clinics
Issue:: Volume 60:Issue 3(2020:Summer)
Page Start:
Record Type:: Journal Article
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4. X-Linked Retinoschisis and a Coats-Like Response in the Setting of Retinopathy of Prematurity. (November 2020)

Authors:: Fan, Kenneth C.; McAllister, Mark A.; Yannuzzi, Nicolas A.; Patel, Nimesh A.; Prakhunhungsit, Supalert; Negron, Catherin I.; Capó, Hilda; Berrocal, Audina M.
Journal:: Journal of vitreoretinal diseases
Issue:: Volume 4:Number 6(2020)
Page Start:: 525
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗