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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

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

PREVALENCE AND AETIOLOGY OF LYMPHOEDEMA AFTER BREAST CANCER TREATMENT IN SOUTHERN TASMANIA

Journal article

Edwards TL., (2000), ANZ Journal of Surgery, 70, 412 - 418