Assessment of the Electronic Retinal Implant Alpha AMS in Restoring Vision to Blind Patients with End-Stage Retinitis Pigmentosa
Journal article
Edwards TL. et al, (2018), Ophthalmology, 125, 432 - 443
Novel non-contiguous exon duplication in choroideremia
Journal article
Edwards TL. et al, (2018), Clinical Genetics, 93, 144 - 148
The Spectrum of CHM Gene Mutations in Choroideremia and Their Relationship to Clinical Phenotype
Journal article
Simunovic MP. et al, (2016), Investigative Opthalmology & Visual Science, 57, 6033 - 6033
A Qualitative and Quantitative Assessment of Fundus Autofluorescence Patterns in Patients With Choroideremia
Journal article
Jolly JK. et al, (2016), Investigative Opthalmology & Visual Science, 57, 4498 - 4498
Correlation of Optical Coherence Tomography and Autofluorescence in the Outer Retina and Choroid of Patients With Choroideremia
Journal article
Xue K. et al, (2016), Investigative Opthalmology & Visual Science, 57, 3674 - 3674
Visual Acuity after Retinal Gene Therapy for Choroideremia
Journal article
Edwards TL. et al, (2016), New England Journal of Medicine, 374, 1996 - 1998
Correlation of Retinal Structure and Function in Choroideremia Carriers
Journal article
Edwards TL. et al, (2015), Ophthalmology, 122, 1274 - 1276
Outcomes following cataract surgery in choroideremia
Journal article
Edwards TL. et al, (2015), Eye, 29, 460 - 464
Bleb Management
Chapter
Edwards TL. et al, (2015), International Society of Glaucoma Surgery - ISGS Textbook on Glaucoma Surgery
Molteno Glaucoma Drainage Device
Chapter
Edwards TL. et al, (2015), International Society of Glaucoma Surgery - ISGS Textbook on Glaucoma Surgery
The Test–Retest Reliability of the Photopic Negative Response (PhNR)
Journal article
Tang J. et al, (2014), Translational Vision Science & Technology, 3, 1 - 1
Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations
Journal article
Edwards TL. et al, (2012), Clinical & Experimental Ophthalmology, 40, 476 - 483
Telemedicine model to prevent blindness from familial glaucoma
Journal article
Staffieri SE. et al, (2011), Clinical & Experimental Ophthalmology, 39, 760 - 765
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling
Journal article
Tsang HTH. et al, (2009), Human Molecular Genetics, 18, 3805 - 3821
Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5
Journal article
Edwards TL. et al, (2009), Biochemical Journal, 423, 31 - 39
Is Second Eye Involvement in Leber's Hereditary Optic Neuropathy Due to Retro-Chiasmal Spread of Apoptosis?
Journal article
Edwards TL. et al, (2007), Neuro-Ophthalmology, 31, 87 - 98
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners
Journal article
Sanderson CM. et al, (2006), Human Molecular Genetics, 15, 307 - 318
The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B
Journal article
Reid E. et al, (2005), Human Molecular Genetics, 14, 19 - 38
PREVALENCE AND AETIOLOGY OF LYMPHOEDEMA AFTER BREAST CANCER TREATMENT IN SOUTHERN TASMANIA
Journal article
Edwards TL., (2000), ANZ Journal of Surgery, 70, 412 - 418