Visual impairment in children with multiple disabilities in schools for children with special needs in South India von Bhaskaran, Sahithya, Flora, Jeyaseeli, Perumalsamy, Vijayalakshmi, Durairaj, Deepa

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Ocular signs, visual and general developmental outcome in Indian children with radiologically proven periventricular leukomalacia von Vijayalakshmi, Perumalsamy, Flora, Jeyaseeli, Shah, Gargi, Sahithya, Bhaskaran, Gilbert, Clare

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Yoked prisms and cerebral visual impairment: Enhancing the experience of ambient vision von Bhaskaran, Sahithya, Pandurangan, Sneha, Perumalsamy, Vijayalakshmi, Floor, Jeyaseeli

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Mutational screening of LCA genes emphasizing RPE65 in South Indian cohort of patients von Verma, Anshuman, Perumalsamy, Vijayalakshmi, Shetty, Shashikant, Kulm, Maigi, Sundaresan, Periasamy

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Pediatric ophthalmology training in India von Gogate, Parikshit, Biswas, Partha, Perumalsamy, Vijayalakshmi

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Clinical exome sequencing facilitates the understanding of genetic heterogeneity in Leber congenital amaurosis patients with variable phenotype in southern India von Viswarubhiny, Sriee, Anjanamurthy, Rupa, Vanniarajan, Ayyasamy, Bharanidharan, Devarajan, Perumalsamy, Vijayalakshmi, Sundaresan, Periasamy

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Autosomal recessive juvenile onset cataract associated with mutation in BFSP1 von RAMYA DEVI RAMACHANDRAN, PERUMALSAMY, Vijayalakshmi, FIELDING HEJTMANCIK, J

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Optical iridectomy in children with corneal opacities von Sundaresh, Kannan, MS, Jethani, Jitendra, MS, DO, DNB, FNB, Vijayalakshmi, Perumalsamy, MS, DO

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Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea von Devi, Ramachandran Ramya, Vijayalakshmi, Perumalsamy

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Electroretinographic assessment and diagnostic reappraisal of children with visual dysfunction: a prospective study von Vedantham, Vasumathy, Jethani, Jithendra, Vijayalakshmi, Perumalsamy

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Congenital oculomotor nerve palsy due to effects of carotid artery agenesis von Cherungottil, Lakshmi, MS, Shetty, Shashikant, MS, Vijayalakshmi, Perumalsamy, MS, Dwivedi, Malay Kumar, MS, Srinivasan, Kaliappan Gurusamy, MD, Saravanan, Muniasamy, MRCP

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CRYBA4, a Novel Human Cataract Gene, Is Also Involved in Microphthalmia von Billingsley, Gail, Santhiya, Sathiyavedu T., Paterson, Andrew D., Ogata, Koji, Wodak, Shoshana, Hosseini, S. Mohsen, Manisastry, Shyam Manohar, Vijayalakshmi, Perumalsamy, Gopinath, Pudhiya Mundyat, Graw, Jochen, Héon, Elise

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A new surgical “noose” technique for excision of pediatric ocular adnexal and anterior orbital cysts von Arcot Sadagopan, Karthikeyan, DNB, FRCS, Perumalsamy, Vijayalakshmi, MS, DO

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Retinitis pigmentosa associated with blepharophimosis, blue dot cataract and primary inferior oblique overaction: A new syndrome complex? von Vedantham, Vasumathy, Jethani, Jitendra, Agarwal, Anil, Vijayalakshmi, Perumalsamy

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Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population von Devi, Ramachandran Ramya, Reena, Chandrashekar, Vijayalakshmi, Perumalsamy

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Perceptions of eye diseases and eye care needs of children among parents in rural south India: the Kariapatti Pediatric Eye Evaluation Project (KEEP) von Nirmalan, Praveen K, Sheeladevi, Sethu, Tamilselvi, Velayutham, Victor, Arockia C L, Vijayalakshmi, Perumalsamy, Rahmathullah, Lakshmi

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Mutational analysis and genotype-phenotype correlations in southern Indian patients with sporadic and familial aniridia von Dubey, Sushil Kumar, Mahalaxmi, Nagasubramanian, Vijayalakshmi, Perumalsamy, Sundaresan, Periasamy

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Crystallin gene mutations in Indian families with inherited pediatric cataract von Devi, Ramachandran Ramya, Yao, Wenliang, Vijayalakshmi, Perumalsamy, Sergeev, Yuri V, Sundaresan, Periasamy, Hejtmancik, J Fielding

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Intratrochlear steroid injections in acquired Brown syndrome—a case series von Ravilla, Sathya T., Shetty, Shashikant, Perumalsamy, Vijayalakshmi

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Functional and cognitive vision assessment in children with autism spectrum disorder von Bhaskaran, Sahithya, Lawrence, Linda, Flora, Jeyaseeli, Perumalsamy, Vijayalakshmi

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