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Genetics
Citations 151-160 of 255 total displayed.
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Past content
(since May 1998):
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- Laboratory Sciences
Chemokine Receptor CCR5 Expression in Conjunctival Epithelium of Patients With Dry Eye Syndrome
- Abha Gulati; Marta Sacchetti; Stefano Bonini; Reza Dana
Arch Ophthalmol 2006; 124: 710-716.
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- Laboratory Sciences
Endothelin B Receptor in Human Glaucoma and Experimentally Induced Optic Nerve Damage
- Lin Wang; Brad Fortune; Grant Cull; Jin Dong; George A. Cioffi
Arch Ophthalmol 2006; 124: 717-724.
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- Clinical Sciences
Altered Expression of Neurotransmitter Receptors and Neuromediators in Vernal Keratoconjunctivitis
- Laura Motterle; Yolanda Diebold; Amalia Enríquez de Salamanca; Victoria Saez; Carmen Garcia-Vazquez; Michael E. Stern; Margarita Calonge; Andrea Leonardi
Arch Ophthalmol 2006; 124: 462-468.
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- Editorials
Complement Factor H and Macular Degeneration: The Genome Yields an Important Clue
- Janey L. Wiggs
Arch Ophthalmol 2006; 124: 577-578.
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- Clinicopathologic Reports, Case Reports, and Small Case Series
Photodynamic Therapy for Exudative Hamartoma in Tuberous Sclerosis
- Stefan Mennel; Norbert Hausmann; Carsten H. Meyer; Silvia Peter
Arch Ophthalmol 2006; 124: 597-599.
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- Clinical Sciences
Immunohistochemical Evaluation of Conjunctival Fibrillin-1 in Marfan Syndrome
- Anuradha Ganesh; Charles Smith; Wilson Chan; Sheila Unger; Nada Quercia; Maurice Godfrey; Stephen Kraft; Raymond Buncic; Alex Levin
Arch Ophthalmol 2006; 124: 205-209.
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- Ophthalmic Molecular Genetics
A Novel Mutation in the GJA1 Gene in a Family With Oculodentodigital Dysplasia
- José P. C. Vasconcellos; Mônica B. Melo; Rui B. Schimiti; Norisvaldo C. Bressanim; Fernando F. Costa; Vital P. Costa
Arch Ophthalmol 2005; 123: 1422-1426.
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- Clinicopathologic Reports, Case Reports, and Small Case Series
Bilateral, Localized Orbital Neurofibromas and Charcot-Marie-Tooth Disease
- Riad N. Ma’luf; Baha’ N. Noureddin; Nicola G. Ghazi; Ayman N. Tawil; Suha S. Allam
Arch Ophthalmol 2005; 123: 1443-1445.
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- Epidemiology
Genetic Risk of Rhegmatogenous Retinal Detachment: A Familial Aggregation Study
- Sioe Lie Go; Carel B. Hoyng; Caroline C. W. Klaver
Arch Ophthalmol 2005; 123: 1237-1241.
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- Ophthalmic Molecular Genetics
A Novel KIF21A Mutation in a Patient With Congenital Fibrosis of the Extraocular Muscles and Marcus Gunn Jaw-Winking Phenomenon
- Koki Yamada; David G. Hunter; Caroline Andrews; Elizabeth C. Engle
Arch Ophthalmol 2005; 123: 1254-1259.
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