Bernstein PS - Search Results

1

Progressive optic nerve changes in cavitary optic disc anomaly: integration of copy number alteration and cis-expression quantitative trait loci to assess disease etiology.

Hwang ES, Morgan DJ, Pennington KL, Owen LA, Fingert JH, Bernstein PS, DeAngelis MM. Hwang ES, et al. Among authors: bernstein ps. BMC Med Genet. 2019 Apr 27;20(1):63. doi: 10.1186/s12881-019-0800-4. BMC Med Genet. 2019. PMID: 31029096 Free PMC article.

2

Temporal macular thinning associated with X-linked Alport syndrome.

Ahmed F, Kamae KK, Jones DJ, Deangelis MM, Hageman GS, Gregory MC, Bernstein PS. Ahmed F, et al. Among authors: bernstein ps. JAMA Ophthalmol. 2013 Jun;131(6):777-82. doi: 10.1001/jamaophthalmol.2013.1452. JAMA Ophthalmol. 2013. PMID: 23572034 Free PMC article.

3

ABSENCE OF MACULAR DEGENERATION IN A PATIENT WITH ACERULOPLASMINEMIA.

Ronquillo CC, Sauer L, Morgan D, Heckzo JB, Creel DJ, Mamalis N, DeAngelis MM, Hagemann GS, Bernstein PS. Ronquillo CC, et al. Among authors: bernstein ps. Retina. 2019 Sep;39(9):1824-1828. doi: 10.1097/IAE.0000000000002628. Retina. 2019. PMID: 31356495

4

Genetic Epidemiologic Analysis of Hypertensive Retinopathy in an Underrepresented and Rare Federally Recognized Native American Population of the Intermountain West.

Hicks PM, Melendez SAC, Vitale A, Self W, Hartnett ME, Bernstein P, Morgan DJ, Feehan M, Shakoor A, Kim I, Owen LA, DeAngelis MM. Hicks PM, et al. J Community Med Public Health. 2019;3(1):152. Epub 2019 Jun 10. J Community Med Public Health. 2019. PMID: 31475247 Free PMC article.

5

Systemic Disease and Ocular Comorbidity Analysis of Geographically Isolated Federally Recognized American Indian Tribes of the Intermountain West.

Hicks PM, Haaland B, Feehan M, Crandall AS, Pettey JH, Nuttall E, Self W, Hartnett ME, Bernstein P, Vitale A, Shakoor A, Shulman JP, Sieminski SF, Kim I, Owen LA, Murtaugh MA, Noyes A, DeAngelis MM. Hicks PM, et al. J Clin Med. 2020 Nov 7;9(11):3590. doi: 10.3390/jcm9113590. J Clin Med. 2020. PMID: 33171720 Free PMC article.

6

Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene.

Bernstein PS, Tammur J, Singh N, Hutchinson A, Dixon M, Pappas CM, Zabriskie NA, Zhang K, Petrukhin K, Leppert M, Allikmets R. Bernstein PS, et al. Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3331-6. Invest Ophthalmol Vis Sci. 2001. PMID: 11726641

7

MACULAR PIGMENT DISTRIBUTION RESPONSES TO HIGH-DOSE ZEAXANTHIN SUPPLEMENTATION IN PATIENTS WITH MACULAR TELANGIECTASIA TYPE 2.

Choi RY, Gorusupudi A, Wegner K, Sharifzadeh M, Gellermann W, Bernstein PS. Choi RY, et al. Among authors: bernstein ps. Retina. 2017 Dec;37(12):2238-2247. doi: 10.1097/IAE.0000000000001450. Retina. 2017. PMID: 28079755 Free PMC article. Clinical Trial.

8

Long-term follow-up of autosomal dominant Stargardt macular dystrophy (STGD3) subjects enrolled in a fish oil supplement interventional trial.

Choi R, Gorusupudi A, Bernstein PS. Choi R, et al. Among authors: bernstein ps. Ophthalmic Genet. 2018 Jun;39(3):307-313. doi: 10.1080/13816810.2018.1430240. Epub 2018 Jan 29. Ophthalmic Genet. 2018. PMID: 29377748 Free PMC article.

9

Genetic Penetrance of Macular Telangiectasia Type 2.

Ronquillo CC, Wegner K, Calvo CM, Bernstein PS. Ronquillo CC, et al. Among authors: bernstein ps. JAMA Ophthalmol. 2018 Oct 1;136(10):1158-1163. doi: 10.1001/jamaophthalmol.2018.3283. JAMA Ophthalmol. 2018. PMID: 30098143 Free PMC article.

10

Pattern of vitreo-retinal diseases at the national referral hospital in Bhutan: a retrospective, hospital-based study.

Rai BB, Morley MG, Bernstein PS, Maddess T. Rai BB, et al. Among authors: bernstein ps. BMC Ophthalmol. 2020 Feb 13;20(1):51. doi: 10.1186/s12886-020-01335-x. BMC Ophthalmol. 2020. PMID: 32054472 Free PMC article.

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