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Gene Therapy
|
April 2, 2024
A multinational survey of potential participant perspectives on ocular gene therapy
Alexis Ceecee Britten-Jones, Myra B McGuinness, Fred K Chen, et al.
Clinical Genetics
|
August 8, 2023
Genetic testing and gene therapy in retinal diseases: Knowledge and perceptions of optometrists in Australia and New Zealand
Alexis Ceecee Britten-Jones, Heather G Mack, Andrea L Vincent, et al.
Annals of Medicine
|
August 27, 2023
Characterising the diagnosis of genetic maculopathies in a real-world private tertiary retinal practice in Australia: protocol for a retrospective clinical audit
Alexis Ceecee Britten-Jones, Demi Markakis, Robyn H Guymer, et al.
Translational Vision Science & Technology
|
February 8, 2022
Measurement Properties of the Attitudes to Gene Therapy for the Eye (AGT-Eye) Instrument for People With Inherited Retinal Diseases
Myra B McGuinness, Alexis Ceecee Britten-Jones, Lauren N Ayton, et al.
Journal of the Endocrine Society
|
June 7, 2022
The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing
Mark Stevenson, Alistair T Pagnamenta, Heather G Mack, et al.
Clinical & Experimental Optometry
|
September 15, 2024
Forty-year odyssey to Refsum disease diagnosis: impact of diagnostic delay on effective treatment
Parker Truong, Heather G Mack, Andrew B Metha, et al.
Clinical & Experimental Ophthalmology
|
April 10, 2025
Retinal Gene Therapy: Perceptions of Ophthalmologists in Australia and New Zealand
John O T Britton, Heather G Mack, Andrea L Vincent, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
April 21, 2022
Genetic Testing of Inherited Retinal Disease in Australian Private Tertiary Ophthalmology Practice
Sena A Gocuk, Yuanzhang Jiao, Alexis Ceecee Britten-Jones, et al.
Ophthalmic Genetics
|
December 29, 2022
<i>KCTD1</i> and Scalp-Ear-Nipple ('Finlay-Marks') syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains
Dongmao Wang, Paul Trevillian, Stephen May, et al.
BMJ Open
|
June 23, 2021
Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey
Heather G Mack, Fred K Chen, John Grigg, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 65) with videos related to
Sort By:
Page
of 7
Gene Therapy
|
April 2, 2024
A multinational survey of potential participant perspectives on ocular gene therapy
Alexis Ceecee Britten-Jones, Myra B McGuinness, Fred K Chen, et al.
Clinical Genetics
|
August 8, 2023
Genetic testing and gene therapy in retinal diseases: Knowledge and perceptions of optometrists in Australia and New Zealand
Alexis Ceecee Britten-Jones, Heather G Mack, Andrea L Vincent, et al.
Annals of Medicine
|
August 27, 2023
Characterising the diagnosis of genetic maculopathies in a real-world private tertiary retinal practice in Australia: protocol for a retrospective clinical audit
Alexis Ceecee Britten-Jones, Demi Markakis, Robyn H Guymer, et al.
Translational Vision Science & Technology
|
February 8, 2022
Measurement Properties of the Attitudes to Gene Therapy for the Eye (AGT-Eye) Instrument for People With Inherited Retinal Diseases
Myra B McGuinness, Alexis Ceecee Britten-Jones, Lauren N Ayton, et al.
Journal of the Endocrine Society
|
June 7, 2022
The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing
Mark Stevenson, Alistair T Pagnamenta, Heather G Mack, et al.
Clinical & Experimental Optometry
|
September 15, 2024
Forty-year odyssey to Refsum disease diagnosis: impact of diagnostic delay on effective treatment
Parker Truong, Heather G Mack, Andrew B Metha, et al.
Clinical & Experimental Ophthalmology
|
April 10, 2025
Retinal Gene Therapy: Perceptions of Ophthalmologists in Australia and New Zealand
John O T Britton, Heather G Mack, Andrea L Vincent, et al.
Clinical Ophthalmology (Auckland, N.Z.)
|
April 21, 2022
Genetic Testing of Inherited Retinal Disease in Australian Private Tertiary Ophthalmology Practice
Sena A Gocuk, Yuanzhang Jiao, Alexis Ceecee Britten-Jones, et al.
Ophthalmic Genetics
|
December 29, 2022
<i>KCTD1</i> and Scalp-Ear-Nipple ('Finlay-Marks') syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains
Dongmao Wang, Paul Trevillian, Stephen May, et al.
BMJ Open
|
June 23, 2021
Perspectives of people with inherited retinal diseases on ocular gene therapy in Australia: protocol for a national survey
Heather G Mack, Fred K Chen, John Grigg, et al.
Page
of 7