Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 gene

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Ophthalmic Genetics, Vol. 24, Iss. 4, 2003-12 ,pp. : 233-245

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Ocular Findings in Gillespie-Like Syndrome: Association with a New PAX6 Mutation

By Ticho Benjamin H.   Hilchie-Schmidt Clair   Egel Robert T.   Traboulsi Elias I.   Howarth Rachel J.   Robinson David  

Ophthalmic Genetics, Vol. 27, Iss. 4, 2006-12 ,pp. : 145-149

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Anterior Segment Abnormalities and Angle-Closure Glaucoma in a Family with a Mutation in the BEST1 Gene and Best Vitelliform Macular Dystrophy

By Wittström Elisabeth   Ponjavic Vesna   Bondeson Marie-Louise   Andréasson Sten  

Ophthalmic Genetics, Vol. 32, Iss. 4, 2011-11 ,pp. : 217-227

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Effects of endothelin-1 (ET-1) on ocular hemodynamics

By Schmetterer Leopold   Findl Oliver   Strenn Karin   Jilma Bernd   Graselli Ursula   Eichler Hans-Georg   Wolzt Michael  

Current Eye Research, Vol. 16, Iss. 7, 1997-07 ,pp. : 687-692

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Cone-rod dystrophy associated with amelogenesis imperfecta in a child with neurofibromatosis type 1

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Ophthalmic Genetics, Vol. 33, Iss. 1, 2012-03 ,pp. : 34-38

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