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Ophthalmology
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April 9, 2021
Reply
Ayub Qassim, Sean Mullany, Lachlan S W Knight, et al.
BMJ Open
|
July 20, 2022
Quality of life in children with glaucoma: a qualitative interview study in Australia
Lachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Ophthalmology. Glaucoma
|
February 13, 2022
The Caregiver Experience in Childhood Glaucoma: An Interview Study
Lachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Ophthalmology. Glaucoma
|
September 25, 2021
Quality of Life in Adults with Childhood Glaucoma: An Interview Study
Lachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Clinical & Experimental Ophthalmology
|
March 3, 2021
Impact of cardiometabolic factors on retinal vasculature: A 3 × 3, 6 × 6 and 8 × 8-mm ocular coherence tomography angiography study
Michelle T Sun, Sonia Huang, WengOnn Chan, et al.
Cornea
|
March 30, 2022
Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants
Mallika Prem Senthil, Lachlan S W Knight, Deepa Taranath, et al.
Journal of Neurology
|
April 30, 2026
"Getting to diagnosis was an absolute nightmare": survey insights about the lived experience of spinal CSF leak in Australia and Aotearoa New Zealand
Lachlan S W Knight, Rachel L Smith, Alexis Ceecee Britten-Jones, et al.
American Journal of Medical Genetics. Part A
|
November 24, 2020
Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variants
Emmanuelle Souzeau, Owen M Siggs, Francesca Pasutto, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 12, 2025
Axenfeld-Rieger syndrome associated with a megabase-scale inversion separating <i>PITX2</i> from a conserved enhancer locus
Lucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
European Journal of Human Genetics : EJHG
|
March 27, 2026
Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndrome
Lucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
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Search research articles
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Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Ophthalmology
|
April 9, 2021
Reply
Ayub Qassim, Sean Mullany, Lachlan S W Knight, et al.
BMJ Open
|
July 20, 2022
Quality of life in children with glaucoma: a qualitative interview study in Australia
Lachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Ophthalmology. Glaucoma
|
February 13, 2022
The Caregiver Experience in Childhood Glaucoma: An Interview Study
Lachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Ophthalmology. Glaucoma
|
September 25, 2021
Quality of Life in Adults with Childhood Glaucoma: An Interview Study
Lachlan S W Knight, Bronwyn Ridge, Sandra E Staffieri, et al.
Clinical & Experimental Ophthalmology
|
March 3, 2021
Impact of cardiometabolic factors on retinal vasculature: A 3 × 3, 6 × 6 and 8 × 8-mm ocular coherence tomography angiography study
Michelle T Sun, Sonia Huang, WengOnn Chan, et al.
Cornea
|
March 30, 2022
Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants
Mallika Prem Senthil, Lachlan S W Knight, Deepa Taranath, et al.
Journal of Neurology
|
April 30, 2026
"Getting to diagnosis was an absolute nightmare": survey insights about the lived experience of spinal CSF leak in Australia and Aotearoa New Zealand
Lachlan S W Knight, Rachel L Smith, Alexis Ceecee Britten-Jones, et al.
American Journal of Medical Genetics. Part A
|
November 24, 2020
Gene-specific facial dysmorphism in Axenfeld-Rieger syndrome caused by FOXC1 and PITX2 variants
Emmanuelle Souzeau, Owen M Siggs, Francesca Pasutto, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 12, 2025
Axenfeld-Rieger syndrome associated with a megabase-scale inversion separating <i>PITX2</i> from a conserved enhancer locus
Lucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
European Journal of Human Genetics : EJHG
|
March 27, 2026
Non-coding structural variants disrupting conserved PITX2 enhancer loci in Axenfeld-Rieger syndrome
Lucas A Mitchell, Joshua Schmidt, Emmanuelle Souzeau, et al.
Page
of 2