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    Sankara Nethralaya

    EST. 1976
    1,603论文总数
    2.4万引用总数

    Sankara Nethralaya is a not-for-profit missionary institution for ophthalmic care (i.e., an eye hospital) headquartered in Chennai, India. In the name "Sankara Nethralaya", "Sankara" is a reference to Adi Shankaracharya and "Nethralaya" means "The Temple of the Eye". Sankara Nethralaya receives patients from India and abroad. Sankara Nethralaya has over 1000 employees and serves around 1500 patients per day, performing over 100 surgeries per day. The annual revenue as per the taxes is close to US$100 million.Sankara Nethralaya was rated among the top four ophthalmic institutions worldwide in 2020 by Newsweek. Nani A. Palkivala, former Indian ambassador to United States, described Sankara Nethralaya as the "Best managed charitable organization in India".

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    论文(1603)

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    1Predicting Progression to Proliferative Diabetic Retinopathy Using Automated Versus Manual Quantification of Retinal Haemorrhages
    Aditya Verma, Muneeswar G. Nittala, Roxan Mansoori Dara, Marius Facktor, Chaithanya A. Ramachandra,Malavika Bhaskaranand,Sandeep Bhat, Kaushal Solanki,Chaitra Jayadev, Swetha B. Velaga,Gavin Robertson, Bradley Yates,

    To compare automated and manual quantification of retinal haemorrhages in eyes with diabetic retinopathy (DR) and to analyse the risk of progression to proliferative DR (PDR). Retinal haemorrhages on ultra-widefield (UWF) pseudocolor images in eyes with non-proliferative diabetic retinopathy (NPDR) were manually segmented. DR severity was assessed within the seven ETDRS fields at baseline and 1-year follow-up. Lesions were also automatically segmented using EyeRead UWF software (Eyenuk) and the frequency and area of retinal haemorrhages and the average distance of haemorrhages from the optic nerve centre were computed. Manual and automated results were compared and correlated with progression to PDR at one year. Sixty-three eyes with NPDR at baseline were included, of which 29 progressed to PDR over one year. The automated measurements of total haemorrhage frequency, area and the distance from the optic nerve were significantly lower compared to manual grading, but the parameters were significantly correlated (r = 0.5–0.96; all P < 0.001). The distance of the haemorrhages from the optic nerve was found to be a significant risk factor for progression to proliferative DR from both approaches. Automated detection of retinal haemorrhages may serve as a surrogate to the manual grading in predicting the progression to PDR. Although the automated approach detects a lower number of lesions compared to manual grading, the results are correlated and the automatically determined parameters are still predictive of progression.

    2026Eye(2026)引用:2
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    2Congenital Grouped Albinotic Spots of the Retinal Pigment Epithelium-a Case Report.
    Dhanashree Ratra, Devika Damle

    To describe the clinical and multimodal imaging characteristics of congenital grouped albinotic spots (CGAS) and to explore their functional implications using full-field electroretinography (ERG). Two patients with incidentally detected CGAS underwent comprehensive ophthalmic examination, including best-corrected visual acuity, refraction, dilated fundus evaluation, swept-source optical coherence tomography (SSOCT), fundus autofluorescence (FAF) imaging, and full-field ERG. Longitudinal follow-up was available for one case over 7 years. Clinical and imaging findings were qualitatively compared with previously reported CGAS features and with differential diagnoses of flecked retina disorders. Both patients demonstrated numerous, bilaterally symmetrical, flat hypopigmented lesions that were small and round at the posterior pole, sparing the fovea and larger, linear, and radially oriented in the periphery. FAF showed striking hyperautofluorescence corresponding to the hypopigmented patches. SSOCT in both cases showed preserved foveal contour, normal retinal architecture, and intact RPE–photoreceptor complex. Visual acuity was 20/20 in both patients at last examination, after refractive correction. ERG responses were largely within normal reference limits, although each case exhibited minimally reduced photopic responses. CGAS represents a benign, nonprogressive RPE abnormality with characteristic peripheral hypopigmented spots that are paradoxically hyperautofluorescent on FAF and associated with preserved retinal structure and good visual function. FAF and OCT are valuable, non-invasive tools for confirming the diagnosis, delineating lesion extent, and distinguishing CGAS from inherited flecked-retina dystrophies. Additional case series and genetic studies are warranted to clarify underlying mechanisms and potential associations.

    2026Documenta Ophthalmologica(2026)
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    3Lifetime Risk of Perimetric Blindness among Patients with Glaucoma
    Ronnie George,Georgin Jacob,Reni Philip,Raghu Prasad,Gary Lee, Baskaran Mani
    2026INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE(2026)
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    4The Vanishing Golden Fundus: Visualizing the Mizuo-Nakamura Phenomenon in GRK1-associated Oguchi Disease in a Child.
    Vipin Rana,Rupak Roy, Amit Nandan Tripathi
    2026Eye (London, England)(2026)
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    5Pupil, Palsy, and the Puff of Smoke – A Peculiar Association!!
    Selvakumar Ambika, Padma Lakshmi,Olma Veena Noronha, Swatee Vasant Halbe, Nisar Sonam Poonam
    2026Neuro-Ophthalmology(2026)
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    合作机构(100)

    L. V. Prasad 眼科研究所合作论文 40
    Narayana Health合作论文 32
    Aravind Eye Hospital合作论文 31
    新加坡国立大学合作论文 23
    Medical Research Foundation合作论文 21
    印第安纳大学合作论文 20
    新加坡眼科研究所合作论文 20
    新加坡陈笃生医院合作论文 19
    悉尼大学合作论文 18
    西北大学合作论文 17

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