Flinders University Flinders Academic Commons
 

Flinders Academic Commons >

Browsing by Author Hewitt, Alex W

Jump to: 0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
or enter first few letters:   
Sort by: In order: Results/Page Authors/Record:
Showing results 20 to 30 of 30
< previous 
PreviewIssue DateTitleAuthor(s)
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 20 to 30 of 30
< previous 

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2010  Duraspace - Feedback