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Genetic Disorders
Citations 61-70 of 188 total displayed.
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Past content
(since May 1998):
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- Clinicopathologic Reports, Case Reports, and Small Case Series
Neovascular Glaucoma From Advanced Coats Disease as the Initial Manifestation of Facioscapulohumeral Dystrophy in a 2-Year-Old Child
- Carol L. Shields; Jonathan Zahler; Naomi Falk; Minoru Furuta; Ralph C. Eagle Jr; Luis E. Bello Espinosa; Philip R. Fischer; Jerry A. Shields
Arch Ophthalmol 2007; 125: 840-842.
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- Clinical Sciences
Sweep Visual Evoked Potential Testing as a Predictor of Recognition Acuity in Albinism
- Yasmin S. Bradfield; Thomas D. France; James Verhoeve; Ronald E. Gangnon
Arch Ophthalmol 2007; 125: 628-633.
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- Laboratory Sciences
Effect of Smad7 Gene Overexpression on Transforming Growth Factor Induced Retinal Pigment Fibrosis in a Proliferative Vitreoretinopathy Mouse Model
- Shizuya Saika; Osamu Yamanaka; Iku Nishikawa-Ishida; Ai Kitano; Kathleen C. Flanders; Yuka Okada; Yoshitaka Ohnishi; Yuji Nakajima; Kazuo Ikeda
Arch Ophthalmol 2007; 125: 647-654.
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- Clinicopathologic Reports, Case Reports, and Small Case Series
Optic Disc Tuber
- Michael C. Brodsky; Ammar N. Safar
Arch Ophthalmol 2007; 125: 710-712.
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- Book and Software Reviews
Retina, 4th ed
- Thomas S. Stevens
Arch Ophthalmol 2007; 125: 719-a-720-a.
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- Book and Software Reviews
Cornea Atlas, 2nd ed
- Matthew J. Thompson
Arch Ophthalmol 2007; 125: 719.
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- Clinicopathologic Reports, Case Reports, and Small Case Series
Orbital Rhabdomyosarcoma in Li-Fraumeni Syndrome
- Deborah Y. Chong; Hakan Demirci; Shawn M. Ronan; Andrew Flint; Victor M. Elner
Arch Ophthalmol 2007; 125: 566-569.
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- Book and Software Reviews
A Compendium of Inherited Disorders and the Eye
- David M. Gamm
Arch Ophthalmol 2007; 125: 582.
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- Laboratory Sciences
Ocular Pathologic Findings of Neurofibromatosis Type 2
- Margaret E. McLaughlin; Susan M. Pepin; Mia MacCollin; Pitipol Choopong; Simmons Lessell
Arch Ophthalmol 2007; 125: 389-394.
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- Correspondence
Familial Exudative Vitreoretinopathy and Osteoporosis-Pseudoglioma Syndrome Caused by a Mutation in the LRP5 Gene
- Kimberly A. Drenser; Michael T. Trese
Arch Ophthalmol 2007; 125: 431-b-432-b.
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