Found: 22
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Management of Pediatric Aphakic Glaucoma With Vitrectomy and Tube Shunts.
- Published in:
- Journal of Pediatric Ophthalmology & Strabismus, 2016, v. 53, n. 6, p. 339, doi. 10.3928/01913913-20160818-01
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- Publication type:
- Article
Exome-based investigation of the genetic basis of human pigmentary glaucoma.
- Published in:
- BMC Genomics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12864-021-07782-0
- By:
- Publication type:
- Article
A Genome-Wide Association Study for Primary Open Angle Glaucoma and Macular Degeneration Reveals Novel Loci.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058657
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- Publication type:
- Article
GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery.
- Published in:
- JAMA Ophthalmology, 2023, v. 141, n. 9, p. 872, doi. 10.1001/jamaophthalmol.2023.3535
- By:
- Publication type:
- Article
Myocilin Mutations in Patients With Normal-Tension Glaucoma.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Ptosis Masquerading as Progression of Severe Glaucoma.
- Published in:
- JAMA Ophthalmology, 2017, v. 139, n. 9, p. 1
- By:
- Publication type:
- Article
Thin Central Corneal Thickness and Early-Onset Glaucoma in Lacrimo-auriculo-dento-digital Syndrome.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Successful Long-term Management of Iris Flocculi and Miosis in a Patient With a Strong Family History of Thoracic Aortic Aneurysms and Dissections Associated With an MYH11 Mutation.
- Published in:
- JAMA Ophthalmology, 2014, v. 132, n. 6, p. 778, doi. 10.1001/jamaophthalmol.2014.294
- By:
- Publication type:
- Article
Thin Central Corneal Thickness and Early-Onset Glaucomain Lacrimo-auriculo-dento-digital Syndrome.
- Published in:
- JAMA Ophthalmology, 2014, v. 132, n. 6, p. 782, doi. 10.1001/jamaophthalmol.2014.306
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- Publication type:
- Article
Intralesional Ethanol for an Unresectable Epithelial Inclusion Cyst.
- Published in:
- JAMA Ophthalmology, 2013, v. 131, n. 2, p. 262, doi. 10.1001/2013.jamaophthalmol.113
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- Publication type:
- Article
TANK-BINDING KINASE 1 (TBK1) GENE AND OPEN-ANGLE GLAUCOMAS (AN AMERICAN OPHTHALMOLOGICAL SOCIETY THESIS).
- Published in:
- Transactions of the American Ophthalmological Society, 2016, v. 114, p. 1
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- Publication type:
- Article
LADD syndrome with glaucoma is caused by a novel gene.
- Published in:
- Molecular Vision, 2017, v. 23, p. 179
- By:
- Publication type:
- Article
THE CONTROL OF HEPATITIS B VIRUS INFECTION WITH VACCINE IN YUPIK ESKIMOS.
- Published in:
- American Journal of Epidemiology, 1985, v. 121, n. 6, p. 914, doi. 10.1093/oxfordjournals.aje.a114061
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- Publication type:
- Article
Primary congenital and developmental glaucomas.
- Published in:
- Human Molecular Genetics, 2017, v. 26, p. R28, doi. 10.1093/hmg/ddx205
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- Publication type:
- Article
SQSTM1 Mutations and Glaucoma.
- Published in:
- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0156001
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- Publication type:
- Article
Reply.
- Published in:
- Journal of Infectious Diseases, 1986, v. 153, n. 6, p. 1180, doi. 10.1093/infdis/153.6.1180
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- Publication type:
- Article
Reply.
- Published in:
- Journal of Infectious Diseases, 1986, v. 153, n. 1, p. 171, doi. 10.1093/infdis/153.1.171a
- By:
- Publication type:
- Article
The Long-Term Serological Course of Asymptomatic Hepatitis B Virus Carriers and the Development of Primary Hepatocellular Carcinoma.
- Published in:
- Journal of Infectious Diseases, 1985, v. 151, n. 4, p. 604
- By:
- Publication type:
- Article
Acute Hepatitis B Virus Infection: Relation of Age to the Clinical Expression of Disease and Subsequent Development of the Carrier State.
- Published in:
- Journal of Infectious Diseases, 1985, v. 151, n. 4, p. 599
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- Publication type:
- Article
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 7, p. 1021, doi. 10.1093/hmg/9.7.1021
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- Publication type:
- Article
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25.
- Published in:
- Nature Genetics, 1998, v. 19, n. 2, p. 140, doi. 10.1038/493
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- Publication type:
- Article
Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.
- Published in:
- Human Molecular Genetics, 1999, v. 8, n. 5, p. 899, doi. 10.1093/hmg/8.5.899
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- Publication type:
- Article