Casey T - Search Results

1

Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataract.

Javadiyan S, Craig JE, Souzeau E, Sharma S, Lower KM, Pater J, Casey T, Hodson T, Burdon KP. Javadiyan S, et al. Among authors: casey t. BMC Res Notes. 2016 Feb 11;9:83. doi: 10.1186/s13104-016-1890-0. BMC Res Notes. 2016. PMID: 26867756 Free PMC article.

2

Identification of a novel oligomerization disrupting mutation in CRYΑA associated with congenital cataract in a South Australian family.

Laurie KJ, Dave A, Straga T, Souzeau E, Chataway T, Sykes MJ, Casey T, Teo T, Pater J, Craig JE, Sharma S, Burdon KP. Laurie KJ, et al. Among authors: casey t. Hum Mutat. 2013 Mar;34(3):435-8. doi: 10.1002/humu.22260. Epub 2013 Jan 17. Hum Mutat. 2013. PMID: 23255486

3

Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome).

Javadiyan S, Craig JE, Sharma S, Lower KM, Casey T, Haan E, Souzeau E, Burdon KP. Javadiyan S, et al. Among authors: casey t. BMC Med Genet. 2017 May 8;18(1):52. doi: 10.1186/s12881-017-0414-7. BMC Med Genet. 2017. PMID: 28482824 Free PMC article.

4

High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia.

Javadiyan S, Craig JE, Souzeau E, Sharma S, Lower KM, Mackey DA, Staffieri SE, Elder JE, Taranath D, Straga T, Black J, Pater J, Casey T, Hewitt AW, Burdon KP. Javadiyan S, et al. Among authors: casey t. G3 (Bethesda). 2017 Oct 5;7(10):3257-3268. doi: 10.1534/g3.117.300109. G3 (Bethesda). 2017. PMID: 28839118 Free PMC article.

5

Pathogenic genetic variants identified in Australian families with paediatric cataract.

Jones JL, McComish BJ, Staffieri SE, Souzeau E, Kearns LS, Elder JE, Charlesworth JC, Mackey DA, Ruddle JB, Taranath D, Pater J, Casey T, Craig JE, Burdon KP. Jones JL, et al. Among authors: casey t. BMJ Open Ophthalmol. 2022 Aug;7(1):e001064. doi: 10.1136/bmjophth-2022-001064. BMJ Open Ophthalmol. 2022. PMID: 36161833 Free PMC article.

6

Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucoma.

Dimasi DP, Hewitt AW, Straga T, Pater J, MacKinnon JR, Elder JE, Casey T, Mackey DA, Craig JE. Dimasi DP, et al. Among authors: casey t. Clin Genet. 2007 Sep;72(3):255-60. doi: 10.1111/j.1399-0004.2007.00864.x. Clin Genet. 2007. PMID: 17718864

7

Can intraoperative use of limbal stay suture in strabismus surgery cause epithelial ingrowth?

Ullrich K, Taranath D, Casey T. Ullrich K, et al. Among authors: casey t. J Pediatr Ophthalmol Strabismus. 2013 Jun 4;50 Online:e21-3. doi: 10.3928/01913913-20130528-01. J Pediatr Ophthalmol Strabismus. 2013. PMID: 23739587

8

Can intraoperative use of limbal stay suture in strabismus surgery cause epithelial ingrowth?

Ullrich K, Taranath D, Casey T. Ullrich K, et al. Among authors: casey t. J Pediatr Ophthalmol Strabismus. 2013 Jun 4;50 Online:e21-3. doi: 10.3928/01913913-20130528-01. J Pediatr Ophthalmol Strabismus. 2013. PMID: 24601432

9

Fryns "Anophthalmia-Plus" syndrome associated with developmental regression.

Wiltshire E, Moore M, Casey T, Smith G, Smith S, Thompson E. Wiltshire E, et al. Among authors: casey t. Clin Dysmorphol. 2003 Jan;12(1):41-3. doi: 10.1097/00019605-200301000-00007. Clin Dysmorphol. 2003. PMID: 12514364

10

Ophthalmic sequelae of Crouzon syndrome.

Gray TL, Casey T, Selva D, Anderson PJ, David DJ. Gray TL, et al. Among authors: casey t. Ophthalmology. 2005 Jun;112(6):1129-34. doi: 10.1016/j.ophtha.2004.12.037. Ophthalmology. 2005. PMID: 15885794

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