Cataract management in children: a review of the literature and current practice across five large UK centres von Self, J. E., Taylor, R., Solebo, A. L., Biswas, S., Parulekar, M., Dev Borman, A., Ashworth, J., McClenaghan, R., Abbott, J., O’Flynn, E., Hildebrand, D., Lloyd, I. C.

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Applanation tonometry in silicone hydrogel contact lens wearers von Allen, R.J, Dev Borman, A, Saleh, G.M

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Ophthalmic histopathology samples – are we sending enough? von DEV BORMAN, A, HASSANI, M, KESHARAJU, R, NADERI, K, GHAZI‐NOURI, S

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A Genotype - Phenotype Study of Childhood Onset Retinal Dystrophies von Dev Borman, A

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Cataract management in children: a review of the literature and current practice across five large UK centres von Self, JE, Taylor, R, Solebo, AL, Biswas, S, Parulekar, M, Dev Borman, A, Ashworth, J, McClenaghan, R, Abbott, J, O’Flynn, E, Hildebrand, D, Lloyd, IC

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Reevaluation of the Retinal Dystrophy Due to Recessive Alleles of RGR With the Discovery of a Cis-Acting Mutation in CDHR1 von Arno, G, Hull, S, Carss, K, Dev-Borman, A, Chakarova, C, Bujakowska, K, van den Born, I, Robson, AG, Holder, GE, Michaelides, M, Cremers, FP, Pierce, E, Raymond, FL, Moore, AT, Webster, AR

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Leber congenital amaurosis associated with AIPL1: Challenges in ascribing disease causation, clinical findings, and implications for gene therapy von Tan, MH, Mackay, DS, Cowing, J, Tran, HV, Smith, AJ, Wright, GA, Dev-Borman, A, Henderson, RH, Moradi, P, Russell-Eggitt, I, MacLaren, RE, Robson, AG, Cheetham, ME, Thompson, DA, Webster, AR, Michaelides, M, Ali, RR, Moore, AT

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Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy von Tan, MH, Mackay, DS, Cowing, J, Tran, HV, Smith, AJ, Wright, GA, Dev-Borman, A, Henderson, RH, Moradi, P, Russell-Eggitt, I, MacLaren, RE, Robson, AG, Cheetham, ME, Thompson, DA, Webster, AR, Michaelides, M, Ali, RR, Moore, AT

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Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease von Payne, Felicity, Lim, Koini, Girousse, Amandine, Brown, Rebecca J., Kory, Nora, Robbins, Ann, Xue, Yali, Sleigh, Alison, Cochran, Elaine, Adams, Claire, Borman, Arundhati Dev, Russel-Jones, David, Gorden, Phillip, Semple, Robert K., Saudek, Vladimir, O'Rahilly, Stephen, Walther, Tobias C., Barroso, Inês, Savage, David B.

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NMNAT1 mutations cause Leber congenital amaurosis von Falk, Marni J, Zhang, Qi, Nakamaru-Ogiso, Eiko, Kannabiran, Chitra, Fonseca-Kelly, Zoe, Chakarova, Christina, Audo, Isabelle, Mackay, Donna S, Zeitz, Christina, Borman, Arundhati Dev, Staniszewska, Magdalena, Shukla, Rachna, Palavalli, Lakshmi, Mohand-Said, Saddek, Waseem, Naushin H, Jalali, Subhadra, Perin, Juan C, Place, Emily, Ostrovsky, Julian, Xiao, Rui, Bhattacharya, Shomi S, Consugar, Mark, Webster, Andrew R, Sahel, José-Alain, Moore, Anthony T, Berson, Eliot L, Liu, Qin, Gai, Xiaowu, Pierce, Eric A

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Autonomic instability, arrhythmia and visual impairment in a new presentation of MTFMT‐related mitochondrial disease von Howard, Caoimhe, Dev‐Borman, Arundhati, Stokes, John, O'Rourke, Declan, Gillespie, Ciara, Twomey, Eilish, Knerr, Ina, Boruah, Ritma

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Nonaccidental injury presenting as unilateral retinal detachment in two infants von Sornalingam, Krishanthy, Borman, Arundhati Dev, Ashworth, Jane

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Benign Yellow Dot Maculopathy: A New Macular Phenotype von Dev Borman, Arundhati, Rachitskaya, Aleksandra, Suzani, Martina, Sisk, Robert A, Ahmed, Zubair M, Holder, Graham E, Cipriani, Valentina, Arno, Gavin, Webster, Andrew R, Hufnagel, Robert B, Berrocal, Audina, Moore, Anthony T

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RDH12 retinopathy: novel mutations and phenotypic description von Mackay, Donna S, Dev Borman, Arundhati, Moradi, Phillip, Henderson, Robert H, Li, Zheng, Wright, Genevieve A, Waseem, Naushin, Gandra, Mamatha, Thompson, Dorothy A, Bhattacharya, Shomi S, Holder, Graham E, Webster, Andrew R, Moore, Anthony T

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Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic study von Dev Borman, Arundhati, Ocaka, Louise A, Mackay, Donna S, Ripamonti, Caterina, Henderson, Robert H, Moradi, Phillip, Hall, Georgina, Black, Graeme C, Robson, Anthony G, Holder, Graham E, Webster, Andrew R, Fitzke, Fred, Stockman, Andrew, Moore, Anthony T

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Benign Yellow Dot Maculopathy von Dev Borman, Arundhati, MD(Res), FRCOphth, Rachitskaya, Aleksandra, MD, Suzani, Martina, MD, Sisk, Robert A., MD, FACS, Ahmed, Zubair M., PhD, Holder, Graham E., PhD, Cipriani, Valentina, PhD, Arno, Gavin, PhD, Webster, Andrew R., MD(Res), FRCOphth, Hufnagel, Robert B., MD, PhD, Berrocal, Audina, MD, Moore, Anthony T., FRCOphth, FMedSci

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Clinical and Molecular Characterization of Enhanced S-Cone Syndrome in Children von Hull, Sarah, Arno, Gavin, Sergouniotis, Panagiotis I, Tiffin, Peter, Borman, Arundhati Dev, Chandra, Aman, Robson, Anthony G, Holder, Graham E, Webster, Andrew R, Moore, Anthony T

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A Homozygous Mutation in the TUB Gene Associated with Retinal Dystrophy and Obesity von Borman, Arundhati Dev, Pearce, Laura R., Mackay, Donna S., Nagel-Wolfrum, Kerstin, Davidson, Alice E., Henderson, Robert, Garg, Sumedha, Waseem, Naushin H., Webster, Andrew R., Plagnol, Vincent, Wolfrum, Uwe, Farooqi, I. Sadaf, Moore, Anthony T.

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Leber congenital amaurosis associated with AIPL1: challenges in ascribing disease causation, clinical findings, and implications for gene therapy von Tan, Mei Hong, Mackay, Donna S, Cowing, Jill, Tran, Hoai Viet, Smith, Alexander J, Wright, Genevieve A, Dev-Borman, Arundhati, Henderson, Robert H, Moradi, Phillip, Russell-Eggitt, Isabelle, MacLaren, Robert E, Robson, Anthony G, Cheetham, Michael E, Thompson, Dorothy A, Webster, Andrew R, Michaelides, Michel, Ali, Robin R, Moore, Anthony T

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Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations von Mackay, Donna S, Ocaka, Louise A, Borman, Arundhati Dev, Sergouniotis, Panagiotis I, Henderson, Robert H, Moradi, Phillip, Robson, Anthony G, Thompson, Dorothy A, Webster, Andrew R, Moore, Anthony T

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