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Molecular Vision
|
March 13, 2008
Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis
Vedam Lakshmi Ramprasad, Nagasamy Soumittra, Derek Nancarrow, et al.
Clinical Genetics
|
July 11, 2023
Mutation profile of Bardet-Biedl syndrome patients from India: Implicative role of multiallelic rare variants and oligogenic inheritance pattern
Harshavardhini Gnanasekaran, Sathya Priya Chandrasekhar, Suganya Kandeeban, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
February 11, 2018
Surgical outcomes and complications of sutured scleral fixated intraocular lenses in pediatric eyes
Parveen Sen, Vinay Kumar S, Pramod Bhende, et al.
Ophthalmic Genetics
|
June 3, 2017
Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss
Dhandayuthapani Sudha, Irene Rosita Pia Patric, Aparna Ganapathy, et al.
Indian Journal of Ophthalmology
|
March 23, 2019
Enhanced S-cone syndrome: Clinical spectrum in Indian population
Anmol Naik, Dhanashree Ratra, Aniruddha Banerjee, et al.
Indian Journal of Ophthalmology
|
August 19, 2017
Incidence, outcomes, and risk factors for hemorrhagic complications in eyes with polypoidal choroidal vasculopathy following photodynamic therapy in Indian subjects
Pukhraj Rishi, Ekta Rishi, Minal Sharma, et al.
Ophthalmology and Therapy
|
September 24, 2022
Optical Coherence Tomography-Based Choroidal Structural Analysis and Vascularity Index in Best Vitelliform Macular Dystrophy
Xin Wei, Rupak Roy, Kumar Saurabh, et al.
Indian Journal of Ophthalmology
|
June 16, 2023
Next-generation sequencing--based genetic testing and phenotype correlation in retinitis pigmentosa patients from India
Parveen Sen, Natarajan Srikrupa, Puja Maitra, et al.
The British Journal of Ophthalmology
|
January 22, 2016
Comparison of photodynamic therapy, ranibizumab/bevacizumab or combination in the treatment of myopic choroidal neovascularisation: a 9-year-study from a single centre
Pukhraj Rishi, Ekta Rishi, Muna Bhende, et al.
Plos One
|
June 1, 2018
Understanding variable disease severity in X-linked retinoschisis: Does RS1 secretory mechanism determine disease severity?
Dhandayuthapani Sudha, Srividya Neriyanuri, Ramya Sachidanandam, et al.
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of 12
Search research articles
Search
Showing results (91-100 of 112) with videos related to
Sort By:
Page
of 12
Molecular Vision
|
March 13, 2008
Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis
Vedam Lakshmi Ramprasad, Nagasamy Soumittra, Derek Nancarrow, et al.
Clinical Genetics
|
July 11, 2023
Mutation profile of Bardet-Biedl syndrome patients from India: Implicative role of multiallelic rare variants and oligogenic inheritance pattern
Harshavardhini Gnanasekaran, Sathya Priya Chandrasekhar, Suganya Kandeeban, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie
|
February 11, 2018
Surgical outcomes and complications of sutured scleral fixated intraocular lenses in pediatric eyes
Parveen Sen, Vinay Kumar S, Pramod Bhende, et al.
Ophthalmic Genetics
|
June 3, 2017
Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss
Dhandayuthapani Sudha, Irene Rosita Pia Patric, Aparna Ganapathy, et al.
Indian Journal of Ophthalmology
|
March 23, 2019
Enhanced S-cone syndrome: Clinical spectrum in Indian population
Anmol Naik, Dhanashree Ratra, Aniruddha Banerjee, et al.
Indian Journal of Ophthalmology
|
August 19, 2017
Incidence, outcomes, and risk factors for hemorrhagic complications in eyes with polypoidal choroidal vasculopathy following photodynamic therapy in Indian subjects
Pukhraj Rishi, Ekta Rishi, Minal Sharma, et al.
Ophthalmology and Therapy
|
September 24, 2022
Optical Coherence Tomography-Based Choroidal Structural Analysis and Vascularity Index in Best Vitelliform Macular Dystrophy
Xin Wei, Rupak Roy, Kumar Saurabh, et al.
Indian Journal of Ophthalmology
|
June 16, 2023
Next-generation sequencing--based genetic testing and phenotype correlation in retinitis pigmentosa patients from India
Parveen Sen, Natarajan Srikrupa, Puja Maitra, et al.
The British Journal of Ophthalmology
|
January 22, 2016
Comparison of photodynamic therapy, ranibizumab/bevacizumab or combination in the treatment of myopic choroidal neovascularisation: a 9-year-study from a single centre
Pukhraj Rishi, Ekta Rishi, Muna Bhende, et al.
Plos One
|
June 1, 2018
Understanding variable disease severity in X-linked retinoschisis: Does RS1 secretory mechanism determine disease severity?
Dhandayuthapani Sudha, Srividya Neriyanuri, Ramya Sachidanandam, et al.
Page
of 12