Works by Collison, Frederick
Results: 13
Genetic and Clinical Analysis of ABCA4-Associated Disease in African American Patients.
- Published in:
- Human Mutation, 2014, v. 35, n. 10, p. 1187, doi. 10.1002/humu.22626
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- Article
Comment on Rosa et al. Optic Nerve Drusen Evaluation: A Comparison between Ultrasound and OCT. J. Clin. Med. 2022, 11, 3715.
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- 2023
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- Publication type:
- Letter to the Editor
Analysis of the ABCA4 genomic locus in Stargardt disease.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu396
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- Article
Whole Exome Sequencing Identifies an Adult-Onset Case of Methylmalonic Aciduria and Homocystinuria Type C (cblC) with Non-Syndromic Bull’s Eye Maculopathy.
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- Ophthalmic Genetics, 2015, v. 36, n. 3, p. 270, doi. 10.3109/13816810.2015.1010736
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- Article
Resolution of Mid-Peripheral Schisis in X-Linked Retinoschisis with the Use of Dorzolamide.
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- Ophthalmic Genetics, 2014, v. 35, n. 2, p. 125, doi. 10.3109/13816810.2013.779383
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- Article
Retrolaminar cerebrospinal fluid pressure in compression of the intracranial optic nerves and chiasm.
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- Acta Ophthalmologica (1755375X), 2011, v. 89, n. 5, p. e476, doi. 10.1111/j.1755-3768.2011.02195.x
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- Article
Safety and Proof-of-Concept Study of Oral QLT091001 in Retinitis Pigmentosa Due to Inherited Deficiencies of Retinal Pigment Epithelial 65 Protein (RPE65) or Lecithin:Retinol Acyltransferase (LRAT).
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- PLoS ONE, 2015, v. 10, n. 12, p. 1, doi. 10.1371/journal.pone.0143846
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- Article
Pathognomonic macular ripples are revealed by polarized infrared retinal imaging.
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- Experimental Biology & Medicine, 2021, v. 246, n. 20, p. 2202, doi. 10.1177/15353702211021089
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- Article
Analysis of the ABCA4 genomic locus in Stargardt disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6797, doi. 10.1093/hmg/ddu396
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- Publication type:
- Article
Two-color pupillometry in KCNV2 retinopathy.
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- Documenta Ophthalmologica, 2019, v. 139, n. 1, p. 11, doi. 10.1007/s10633-019-09691-w
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- Publication type:
- Article
Abnormal 8-Hz flicker electroretinograms in carriers of X-linked retinoschisis.
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- Documenta Ophthalmologica, 2016, v. 133, n. 1, p. 61, doi. 10.1007/s10633-016-9551-0
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- Article
Two-color pupillometry in enhanced S-cone syndrome caused by NR2E3 mutations.
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- Documenta Ophthalmologica, 2016, v. 132, n. 3, p. 157, doi. 10.1007/s10633-016-9535-0
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- Article
Rod and cone contributions to the dark-adapted 15-Hz flicker electroretinogram.
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- Documenta Ophthalmologica, 2015, v. 130, n. 2, p. 111, doi. 10.1007/s10633-015-9480-3
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- Publication type:
- Article