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1دورية أكاديمية
المؤلفون: Susmita Chowdhury, Prakash Chermakani, Girish Baliga, Rupa Anjanamurthy, Periasamy Sundaresan
المصدر: Indian Journal of Ophthalmology, Vol 72, Iss 6, Pp 902-911 (2024)
مصطلحات موضوعية: cell adhesion, negative erg, photoreceptors, rs1 gene, retinoschisis, spoke wheel-like macula, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: https://journals.lww.com/10.4103/IJO.IJO_2525_23Test; https://doaj.org/toc/0301-4738Test; https://doaj.org/toc/1998-3689Test
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2دورية أكاديمية
المؤلفون: Sriee Viswarubhiny, Rupa Anjanamurthy, Ayyasamy Vanniarajan, Devarajan Bharanidharan, Vijayalakshmi Perumalsamy, Periasamy Sundaresan
المصدر: Eye and Vision, Vol 8, Iss 1, Pp 1-11 (2021)
مصطلحات موضوعية: Leber congenital amaurosis, Clinical exome sequencing, Southern India, Molecular diagnosis, Genotype-phenotype correlation, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2326-0254Test
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3دورية أكاديمية
المؤلفون: Rajendran Kadarkarai Raj, Pankaja Dhoble, Rupa Anjanamurthy, Prakash Chermakani, Manojkumar Kumaran, Bharanidharan Devarajan, Periasamy Sundaresan
المصدر: Eye and Vision, Vol 7, Iss 1, Pp 1-10 (2020)
مصطلحات موضوعية: Stargardt, ABCA4, Macular degeneration, Yellow white flecks, Mutation detection, South Indian population, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2326-0254Test
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4دورية أكاديمية
المؤلفون: Vidya Raja, Shiva Krishna Manthravadi, Rupa Anjanamurthy
المصدر: Indian Journal of Ophthalmology, Vol 70, Iss 7, Pp 2657-2658 (2022)
مصطلحات موضوعية: angle-closure glaucoma, autosomal recessive bestrophinopathy, electro-oculography, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: http://www.ijo.in/article.asp?issn=0301-4738;year=2022;volume=70;issue=7;spage=2657;epage=2658;aulast=RajaTest; https://doaj.org/toc/0301-4738Test; https://doaj.org/toc/1998-3689Test
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5دورية أكاديمية
المصدر: Indian Journal of Ophthalmology, Vol 67, Iss 10, Pp 1768-1771 (2019)
مصطلحات موضوعية: Closantel, reversible blindness, side effect, toxicity, Ophthalmology, RE1-994
وصف الملف: electronic resource
العلاقة: http://www.ijo.in/article.asp?issn=0301-4738;year=2019;volume=67;issue=10;spage=1768;epage=1771;aulast=KumarTest; https://doaj.org/toc/0301-4738Test; https://doaj.org/toc/1998-3689Test
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6دورية أكاديمية
المؤلفون: Susmita Chowdhury (2836532), Roopam Duvesh (11668227), Manojkumar Kumaran (6850169), Rupa Anjanamurthy (8272011), Jayant Kumar (1780936), Ayyasamy Vanniarajan (19102), Bharanidharan Devarajan (6850175), Periasamy Sundaresan (50306)
مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Neuroscience, Cancer, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, BEST1, autosomal recessive bestrophinopathy, trio-whole-exome sequencing, molecular modeling, South India
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7دورية أكاديمية
المؤلفون: Sriee Viswarubhiny (10761104), Rupa Anjanamurthy (8272011), Ayyasamy Vanniarajan (19102), Devarajan Bharanidharan (10761107), Vijayalakshmi Perumalsamy (458889), Periasamy Sundaresan (50306)
مصطلحات موضوعية: Genetics, Leber congenital amaurosis, Clinical exome sequencing, Southern India, Molecular diagnosis, Genotype-phenotype correlation
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8
المؤلفون: Vijayalakshmi Perumalsamy, Rupa Anjanamurthy, Periasamy Sundaresan, Devarajan Bharanidharan, Ayyasamy Vanniarajan, Sriee Viswarubhiny
المصدر: Eye and Vision, Vol 8, Iss 1, Pp 1-11 (2021)
Eye and Visionمصطلحات موضوعية: 0301 basic medicine, Retinal degeneration, Candidate gene, Genotype-phenotype correlation, medicine.disease_cause, Leber congenital amaurosis, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Retinitis pigmentosa, medicine, Exome, Exome sequencing, Genetics, Sanger sequencing, Mutation, Genetic heterogeneity, business.industry, Research, RE1-994, medicine.disease, Southern India, eye diseases, Clinical exome sequencing, Ophthalmology, 030104 developmental biology, 030221 ophthalmology & optometry, symbols, sense organs, Molecular diagnosis, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5fbc5a127d04fe343a86903b221923eTest
https://doaj.org/article/25f9a15be55f4885afed5e711f44e48fTest -
9
المؤلفون: Bharanidharan Devarajan, Roopam Duvesh, Jayant Kumar, Ayyasamy Vanniarajan, Manojkumar Kumaran, Susmita Chowdhury, Periasamy Sundaresan, Rupa Anjanamurthy
مصطلحات موضوعية: Proband, Genetics, Ophthalmology, Retinal Disorder, Pediatrics, Perinatology and Child Health, Mutation (genetic algorithm), Genotype, Biology, Phenotype, Genetics (clinical), Retinal Dystrophies, Autosomal recessive bestrophinopathy, Exome sequencing
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7203e3ea992bd81b0efd129d11d706Test
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10
المؤلفون: Periasamy Sundaresan, Chitaranjan Mishra, Roopam Duvesh, Susmita Chowdhury, Rupa Anjanamurthy, NareshBabu Kannan, Kim Ramasamy
المصدر: Indian Journal of Ophthalmology - Case Reports. 2:136
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::342dae6ac9dbf3b8d3c55d4d9f880fabTest
https://doi.org/10.4103/ijo.ijo_1283_21Test