Assessment of the Electronic Retinal Implant Alpha AMS in Restoring Vision to Blind Patients with End-Stage Retinitis Pigmentosa
Edwards TL. et al, (2018), Ophthalmology, 125, 432 - 443
Novel non-contiguous exon duplication in choroideremia
Edwards TL. et al, (2018), Clinical Genetics, 93, 144 - 148
The Spectrum of CHM Gene Mutations in Choroideremia and Their Relationship to Clinical Phenotype
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
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
Xue K. et al, (2016), Investigative Opthalmology & Visual Science, 57, 3674 - 3674
Visual Acuity after Retinal Gene Therapy for Choroideremia
Edwards TL. et al, (2016), New England Journal of Medicine, 374, 1996 - 1998
Correlation of Retinal Structure and Function in Choroideremia Carriers
Edwards TL. et al, (2015), Ophthalmology, 122, 1274 - 1276
Bleb Management
Edwards TL. et al, (2015), International Society of Glaucoma Surgery - ISGS Textbook on Glaucoma Surgery
Molteno Glaucoma Drainage Device
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)
Tang J. et al, (2014), Translational Vision Science & Technology, 3, 1 - 1
Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutations
Edwards TL. et al, (2012), Clinical & Experimental Ophthalmology, 40, 476 - 483
Telemedicine model to prevent blindness from familial glaucoma
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
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
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?
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
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
Reid E. et al, (2005), Human Molecular Genetics, 14, 19 - 38
PREVALENCE AND AETIOLOGY OF LYMPHOEDEMA AFTER BREAST CANCER TREATMENT IN SOUTHERN TASMANIA
Edwards TL., (2000), ANZ Journal of Surgery, 70, 412 - 418