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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 1, 2014
Creating a digital retinoscope by combining a mobile smartphone camera and a retinoscope
Weng Onn Chan, Matthew Crabb, David Sia, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
February 27, 2014
Multisegment coloboma in a case of Marfan syndrome: another possible effect of increased TGFβ signaling
Shannon K LeBlanc, Deepa Taranath, Scott Morris, et al.
AJP Reports
|
July 5, 2017
Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality
Florencia Angkasa, Leila Mohammadi, Deepa Taranath, et al.
The Australasian Journal of Dermatology
|
January 15, 2014
Intense pulsed light therapy (IPL) induced iritis following treatment for a medial canthal capillary malformation
Matthew Crabb, Weng Onn Chan, Deepa Taranath, et al.
Survey of Ophthalmology
|
May 21, 2023
Fundus fluorescein angiography imaging of retinopathy of prematurity in infants: A review
Michael Kvopka, WengOnn Chan, Stewart R Lake, et al.
Clinical & Experimental Ophthalmology
|
March 20, 2014
Spontaneously resolved infantile glaucoma
Tzu-Ting Hsu, Sudha Cugati, Jamie E Craig, et al.
Clinical & Experimental Ophthalmology
|
December 28, 2024
Utilisation of Genetic Testing of Inherited Retinal Diseases in an Australian Public Tertiary Hospital Setting
Jai Ethan Paris, Carmelo Zak Macri, Deepa Taranath, et al.
Plos One
|
September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia
Alpana Dave, Kate Laurie, Sandra E Staffieri, 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.
G3 (Bethesda, Md.)
|
August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
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of 3
Search research articles
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Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 1, 2014
Creating a digital retinoscope by combining a mobile smartphone camera and a retinoscope
Weng Onn Chan, Matthew Crabb, David Sia, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
February 27, 2014
Multisegment coloboma in a case of Marfan syndrome: another possible effect of increased TGFβ signaling
Shannon K LeBlanc, Deepa Taranath, Scott Morris, et al.
AJP Reports
|
July 5, 2017
Orbital Subperiosteal Hematoma in the Newborn Causing Unilateral Proptosis: Ultrasound as First-Line Imaging Modality
Florencia Angkasa, Leila Mohammadi, Deepa Taranath, et al.
The Australasian Journal of Dermatology
|
January 15, 2014
Intense pulsed light therapy (IPL) induced iritis following treatment for a medial canthal capillary malformation
Matthew Crabb, Weng Onn Chan, Deepa Taranath, et al.
Survey of Ophthalmology
|
May 21, 2023
Fundus fluorescein angiography imaging of retinopathy of prematurity in infants: A review
Michael Kvopka, WengOnn Chan, Stewart R Lake, et al.
Clinical & Experimental Ophthalmology
|
March 20, 2014
Spontaneously resolved infantile glaucoma
Tzu-Ting Hsu, Sudha Cugati, Jamie E Craig, et al.
Clinical & Experimental Ophthalmology
|
December 28, 2024
Utilisation of Genetic Testing of Inherited Retinal Diseases in an Australian Public Tertiary Hospital Setting
Jai Ethan Paris, Carmelo Zak Macri, Deepa Taranath, et al.
Plos One
|
September 10, 2013
Mutations in the EPHA2 gene are a major contributor to inherited cataracts in South-Eastern Australia
Alpana Dave, Kate Laurie, Sandra E Staffieri, 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.
G3 (Bethesda, Md.)
|
August 26, 2017
High-Throughput Genetic Screening of 51 Pediatric Cataract Genes Identifies Causative Mutations in Inherited Pediatric Cataract in South Eastern Australia
Shari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
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of 3