Vincent AL - Search Results

1

Senior-Løken syndrome and intracranial hypertension.

Tay SA, Vincent AL. Tay SA, et al. Among authors: vincent al. Ophthalmic Genet. 2020 Aug;41(4):354-357. doi: 10.1080/13816810.2020.1766086. Epub 2020 May 20. Ophthalmic Genet. 2020. PMID: 32432520

2

Analysis of the pre-retinal opacities in Gaucher Disease using spectral domain optical coherent tomography.

Sheck LH, Wilson CJ, Vincent AL. Sheck LH, et al. Among authors: vincent al. Ophthalmic Genet. 2012 Dec;33(4):253-6. doi: 10.3109/13816810.2012.716489. Epub 2012 Sep 6. Ophthalmic Genet. 2012. PMID: 22950450

3

Clinical findings and molecular diagnosis of retinoblastoma in older children.

Sheck LH, Ng YS, Watson M, Vincent AL. Sheck LH, et al. Among authors: vincent al. Ophthalmic Genet. 2013 Dec;34(4):238-42. doi: 10.3109/13816810.2012.752015. Epub 2013 Jan 4. Ophthalmic Genet. 2013. PMID: 23289805

4

A novel rhodopsin point mutation, proline-170-histidine, associated with sectoral retinitis pigmentosa.

Shah SP, Wong F, Sharp DM, Vincent AL. Shah SP, et al. Among authors: vincent al. Ophthalmic Genet. 2014 Dec;35(4):241-7. doi: 10.3109/13816810.2014.924014. Epub 2014 Jun 11. Ophthalmic Genet. 2014. PMID: 24918165

5

ADAMTSL4 assessment in ectopia lentis reveals a recurrent founder mutation in Polynesians.

van Bysterveldt KA, Al Taie R, Ikink W, Oliver VF, Vincent AL. van Bysterveldt KA, et al. Among authors: vincent al, al taie r. Ophthalmic Genet. 2017 Dec;38(6):537-543. doi: 10.1080/13816810.2017.1309552. Epub 2017 Apr 10. Ophthalmic Genet. 2017. PMID: 28394649

6

Albinism and a mitochondrial DNA deletion.

Chilibeck CM, Glamuzina EE, Ung CY, Blakely EL, Taylor RW, Vincent AL. Chilibeck CM, et al. Among authors: vincent al. Ophthalmic Genet. 2020 Jun;41(3):295-298. doi: 10.1080/13816810.2020.1750038. Epub 2020 Apr 15. Ophthalmic Genet. 2020. PMID: 32290753 No abstract available.

7

Molecular and phenotypic investigation of a New Zealand cohort of childhood-onset retinal dystrophy.

Hull S, Kiray G, Chiang JP, Vincent AL. Hull S, et al. Among authors: vincent al. Am J Med Genet C Semin Med Genet. 2020 Sep;184(3):708-717. doi: 10.1002/ajmg.c.31836. Epub 2020 Aug 28. Am J Med Genet C Semin Med Genet. 2020. PMID: 32856788

8

The presence and progression of choroidal neurofibromas in a predominantly pediatric population with neurofibromatosis type-1.

Chilibeck CM, Shah S, Russell HC, Vincent AL. Chilibeck CM, et al. Among authors: vincent al. Ophthalmic Genet. 2021 Jun;42(3):223-229. doi: 10.1080/13816810.2021.1881977. Epub 2021 Feb 17. Ophthalmic Genet. 2021. PMID: 33594930

9

Peripheral pigmented lesions in ABCA4-associated retinopathy.

Al-Ani HH, Sheck L, Vincent AL. Al-Ani HH, et al. Among authors: vincent al. Ophthalmic Genet. 2021 Aug;42(4):383-391. doi: 10.1080/13816810.2021.1897850. Epub 2021 Mar 11. Ophthalmic Genet. 2021. PMID: 33706644

10

Best Vitelliform Macular Dystrophy (BVMD) is a phenocopy of North Carolina Macular Dystrophy (NCMD/MCDR1).

Small KW, Jampol LM, Bakall B, Small L, Wiggins R, Agemy S, Udar N, Avetisjan J, Vincent A, Shaya FS. Small KW, et al. Ophthalmic Genet. 2021 Dec 13:1-11. doi: 10.1080/13816810.2021.2010771. Online ahead of print. Ophthalmic Genet. 2021. PMID: 34895015

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

281 results

Search Page