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Browsing by Author Hewitt, Alex W

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Showing results 11 to 29 of 29
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PreviewIssue DateTitleAuthor(s)
2008Genetic analysis of the clusterin gene in pseudoexfoliation syndrome.Sharma, Shiwani; Burdon, Kathryn Penelope; Craig, Jamie E; Hewitt, Alex W; Wang, Jie Jin; Mackey, David A; Mitchell, Paul; McMellon, Amy E
2008Genetic dissection of myopia: evidence for linkage of ocular axial length to chromosome 5qBrown, Shayne A; MacKinnon, Jane R; Chen, Christine Y; Craig, Jamie E; Martin, Nicholas G; Mackey, David A; Zhu, G; Hewitt, Alex W; Ruddle, Jonathan B; Kearns, Lisa S; Hammond, Christopher J; Montgomery, G W
30-Jul-2012Genetic investigation into the endophenotypic status of central corneal thickness and optic disc parameters in relation to open-angle glaucomaDimasi, David Paul; Burdon, Kathryn Penelope; Hewitt, Alex W; Fitzgerald, J; Wang, Jie Jin; Healey, Paul R; Mitchell, Paul; Mackey, David A; Craig, Jamie E
30-Sep-2013Genetic study of Diabetic Retinopathy: recruitment methodology and analysis of baseline characteristicsKaidonis, Georgia; Abhary, Sotoodeh; Daniell, Mark; Gillies, Mark; Fogarty, Rhys Daniel; Petrovsky, Nikolai; Jenkins, Alicia; Essex, Rohan; Chang, John H; Pal, Bishwanath; Hewitt, Alex W; Burdon, Kathryn Penelope; Craig, Jamie E
2006A glaucoma case-control study of the WDR36 gene D658G sequence variantHewitt, Alex W; Mackey, David A; Craig, Jamie E; Dimasi, David Paul
1-Aug-2012Glaucoma risk alleles at CDKN2B-AS1 are associated with lower intraocular pressure, normal tension glaucoma, and advanced glaucomaBurdon, Kathryn Penelope; Crawford, April; Casson, Robert J; Hewitt, Alex W; Landers, John; Danoy, Patrick; Mackey, David A; Mitchell, Paul; Healey, Paul R; Craig, Jamie E
2007Heritable features of the optic disc: a novel twin method for determining genetic significanceAlward, Wallace L M; Hewitt, Alex W; Poulsen, Johan P; Bennett, Sonya L; Budde, Wido M; Cooper, Richard L; Craig, Jamie E; Fingert, John H; Foster, Paul J; Garway-Heath, David F; Green, Catherine M; Hammond, Christopher J; Hayreh, Sohan S; Jonas, Jost B; Kaufman, Paul L; Miller, Neil R; Morgan, William H; Newman, Nancy J; Quigley, Harry A; Samples, John R; Spaeth, George L; Pesudovs, Konrad; Mackey, David A
28-Feb-2013Higher prevalence of Myocilin mutations in advanced glaucoma in comparison with less advanced disease in an Australasian disease registrySouzeau, Emmanuelle; Burdon, Kathryn Penelope; Dubowsky, A; Grist, S; Usher, Bronwyn; Fitzgerald, JT; Crawford, April; Hewitt, Alex W; Goldberg, Ivan; Mills, Richard Arthur; Ruddle, Jonathan B; Landers, John; Mackey, David A; Craig, Jamie E
2006Influence of photodynamic therapy for age related macular degeneration upon subjective vision related quality of lifeHewitt, Alex W; Jeganathan, Swetha; Kidd, Juanita E; Pesudovs, Konrad; Verma, Nitin
2005Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucomaDimasi, David Paul; Hewitt, Alex W; Green, Catherine M; Mackey, David A; Craig, Jamie E
2008Myocilin allele-specific glaucoma phenotype databaseCraig, Jamie E; Hewitt, Alex W; Mackey, David A
2006A myocilin Gln368STOP homozygote does not exhibit a more severe glaucoma phenotype than heterozygous casesHewitt, Alex W; Bennett, Sonya L; Dimasi, David Paul; Craig, Jamie E; Mackey, David A
2007Myocilin Gly252Arg mutation and glaucoma of intermediate severity in caucasian individualsHewitt, Alex W; Bennett, Sonya L; Richards, J E; Dimasi, David Paul; Booth, Adam P; Inglehearn, Chris; Anwar, Rashida; Yamamoto, Tetsuya; Fingert, John H; Heon, Elise; Craig, Jamie E; Mackey, David A
2007The optic nerve head in myocilin glaucomaHewitt, Alex W; Bennett, Sonya L; Fingert, John H; Cooper, Richard L; Stone, Edwin M; Craig, Jamie E; Mackey, David A
26-Sep-2012The p53 codon 72 PRO/PRO genotype may be associated with initial central visual field defects in Caucasians with primary open angle glaucomaWiggs, Janey L; Hewitt, Alex W; Fan, Bao Jian; Wang, Dan Yi; O'Brien, Colm; Realini, Anthony; Craig, Jamie E; Dimasi, David Paul; Mackey, David A; Haines, Jonathan L; Pasquale, Louis R; Figueiredo Sena, Dayse R
2007Prevalence of CYP1B1 mutations in Australian patients with primary congenital glaucomaElder, James E; Casey, T; Mackey, David A; Craig, Jamie E; MacKinnon, Jane R; Hewitt, Alex W; Dimasi, David Paul; Pater, John Brian; Straga, Tania
2006The role of the Met98Lys optineurin variant in inherited optic nerve diseasesCraig, Jamie E; Hewitt, Alex W; Dimasi, David Paul; Howell, Neil; Toomes, Carmel; Cohn, Amy C; Mackey, David A
Jul-2005The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.McKay, James D; Patterson, B; Craig, Jamie E; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Hewitt, Alex W; Cohn, Amy C; Kerdraon, Y; Mackey, David A
2005The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genesMcKay, James D; Patterson, B; Russell-Eggit, Isabelle M; Wirth, M Gabriela; Burdon, Kathryn Penelope; Cohn, Amy C; Kerdraon, Y; Mackey, David A; Craig, Jamie E; Hewitt, Alex W
Showing results 11 to 29 of 29
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