IFT80 mutations cause a novel complex ciliopathy phenotype with retinal degeneration von Moran, J., G. Sanderson, K., Maynes, J., Vig, A., Batmanabane, V., Kannu, P., Tavares, E., Vincent, A., Héon, E.

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The combination of vestibular impairment and congenital sensorineural hearing loss predisposes patients to ocular anomalies, including Usher syndrome von Kletke, S., Batmanabane, V., Dai, T., Vincent, A., Li, S., Gordon, K.A., Papsin, B.C., Cushing, S.L., Héon, E.

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Liver anomalies as a phenotype parameter of Bardet-Biedl syndrome von Branfield Day, L., Quammie, C., Héon, E., Bhan, A., Batmanabane, V., Dai, T., Kamath, B.M.

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Spectrum of Leptospira species identified in patients with leptospiral uveitis in an ophthalmological institute in South India von Batmanabane, V, Chidambaranathan, GP, Rathinam, S

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Spectrum of Leptospira species identified in patients with leptospiral uveitis in an ophthalmological institute in South India von Batmanabane, V, Chidambaranathan, G P, Rathinam, S

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Morphological patterns of indirect choroidal rupture on spectral domain optical coherence tomography von Nair, Unnikrishnan, Soman, Manoj, Ganekal, Sunil, Batmanabane, Vaishnavi, Nair, Kgr

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The selection and use of essential medicines von WHO Expert Committee

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EYS Mutations Causing Autosomal Recessive Retinitis Pigmentosa: Changes of Retinal Structure and Function with Disease Progression von McGuigan, David B, Heon, Elise, Cideciyan, Artur V, Ratnapriya, Rinki, Lu, Monica, Sumaroka, Alexander, Roman, Alejandro J, Batmanabane, Vaishnavi, Garafalo, Alexandra V, Stone, Edwin M, Swaroop, Anand, Jacobson, Samuel G

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C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations von Gerth-Kahlert, Christina, Tiwari, Amit, Hanson, James V M, Batmanabane, Vaishnavi, Traboulsi, Elias, Pennesi, Mark E, Al-Qahtani, Abdullah A, Lam, Byron L, Heckenlively, John, Zweifel, Sandrine A, Vincent, Ajoy, Fierz, Fabienne, Barthelmes, Daniel, Branham, Kari, Khan, Naheed, Bahr, Angela, Baehr, Luzy, Magyar, István, Koller, Samuel, Azzarello-Burri, Silvia, Niedrist, Dunja, Heon, Elise, Berger, Wolfgang

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C2orf71 Mutations as a Frequent Cause of Autosomal-Recessive Retinitis Pigmentosa: Clinical Analysis and Presentation of 8 Novel Mutations von Gerth-Kahlert, Christina, Tiwari, Amit, Hanson, James V M, Batmanabane, Vaishnavi, Traboulsi, Elias, Pennesi, Mark E, Al-Qahtani, Abdullah A, Lam, Byron L, Heckenlively, John, Zweifel, Sandrine A, Vincent, Ajoy, Fierz, Fabienne, Barthelmes, Daniel, Branham, Kari, Khan, Naheed, Bahr, Angela, Baehr, Luzy, Magyar, István, Koller, Samuel, Azzarello-Burri, Silvia, Niedrist, Dunja, Heon, Elise, Berger, Wolfgang

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