The effects of dystrophin gene mutations on the ERG in mice and humans von Cibis, GW, Fitzgerald, KM, Harris, DJ, Rothberg, PG, Rupani, M

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Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations von PILLERS, D.-A. M, FITZGERALD, K. M, WELEBER, R. G, DUNCAN, N. M, RASH, S. M, WHITE, R. A, DWINNELL, S. J, POWELL, B. R, SCHNUR, R. E, RAY, P. N, CIBIS, G. W

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Electroretinography is necessary for spasmus nutans diagnosis von Smith, Daniel E, Fitzgerald, Kathleen, Stass-Isern, Merrill, Cibis, Gerhard W

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Discordant Duane's Retraction Syndrome in Monozygotic Twins von Smith, Daniel E., Cibis, Gerhard W.

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ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy von Fitzgerald, Kathleen M, Cibis, Gerhard W, Gettel, Ann Headrick, Rinaldi, Robert, Harris, David J, White, Robert A

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Dystrophin localization in cone cells von Fitzgerald, K M, Cibis, G W, White, R A

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The negative ERG is not synonymous with nightblindness von Cibis, G W, Fitzgerald, K M

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Electroretinography in congenital idiopathic nystagmus von Cibis, Gerhard W., Fitzgerald, Kathleen M.

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Glaucoma in Sturge-Weber Syndrome von Cibis, Gerhard W., Tripathi, Ramesh C., Tripathi, Brenda J.

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Amblyopia in unilateral congenital ptosis : early detection by sweep visual evoked potential von CIBIS, G. W, FITZGERALD, K. M

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ERG in Duchenne/Becker muscular dystrophy von Fitzgerald, K M, Cibis, G W, White, R A

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Clinical and electroretinographic findings in fetal alcohol syndrome von Hug, Timothy E., Fitzgerald, Kathleen M., Cibis, Gerhard W.

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Familial Total Ophthalmoplegia With Iris Transillumination (a Neurocristopathy) von Cibis, Gerhard W., Tripathi, Ramesh C., Tripathi, Brenda J., Seidel, F. Glen

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Optic nerve hypoplasia in association with brain anomalies and an abnormal electroretinogram von CIBIS, G. W, FITZGERALD, K. M

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Bilateral Choroidal Neonatal Neuroblastoma von Cibis, Gerhard W., Freeman, Arnold I., Pang, Victor, Roloson, Gary J., Case, William F., Ost, Mark, Huntrakoon, Manop, Rothberg, Paul G.

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Autosomal dominant inheritance of a negative electroretinogram phenotype in three generations von Fitzgerald, Kathleen M, Hashimoto, Takao, Hug, Timothy E, Cibis, Gerhard W, Harris, David J

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Pathogenesis of Cataracts in Patients with Lowe's Syndrome von Tripathi, Ramesh C., Cibis, Gerhard W., Tripathi, Brenda J.

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Video vision development assessment (VVDA): combining the Brückner test with eccentric photorefraction for dynamic identification of amblyogenic factors in infants and children von Cibis, G W

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Lenticular Opacities in Carriers of Lowe's Syndrome von Cibis, Gerhard W., Waeltermann, Joanne M., Whitcraft, Chauncey T., Tripathi, Ramesh C., Harris, David J.

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Congenital Pupillary-Iris-Lens Membrane with Goniodysgenesis von Cibis, Gerhard W., Waeltermann, Joanne M., Hurst, Edward, Tripathi, Ramesh C., Richardson, Walter

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