Levin AV - Search Results

1

Ophthalmologic findings in the Cornelia de Lange syndrome.

Shi A, Levin AV. Shi A, et al. Among authors: levin av. Ophthalmic Genet. 2019 Feb;40(1):1-6. doi: 10.1080/13816810.2019.1571617. Epub 2019 Feb 15. Ophthalmic Genet. 2019. PMID: 30767692 Review.

2

Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement.

Kline AD, Moss JF, Selicorni A, Bisgaard AM, Deardorff MA, Gillett PM, Ishman SL, Kerr LM, Levin AV, Mulder PA, Ramos FJ, Wierzba J, Ajmone PF, Axtell D, Blagowidow N, Cereda A, Costantino A, Cormier-Daire V, FitzPatrick D, Grados M, Groves L, Guthrie W, Huisman S, Kaiser FJ, Koekkoek G, Levis M, Mariani M, McCleery JP, Menke LA, Metrena A, O'Connor J, Oliver C, Pie J, Piening S, Potter CJ, Quaglio AL, Redeker E, Richman D, Rigamonti C, Shi A, Tümer Z, Van Balkom IDC, Hennekam RC. Kline AD, et al. Among authors: levin av. Nat Rev Genet. 2018 Oct;19(10):649-666. doi: 10.1038/s41576-018-0031-0. Nat Rev Genet. 2018. PMID: 29995837 Free PMC article. Review.

3

Retinal Findings in Young Children With Increased Intracranial Pressure From Nontraumatic Causes.

Shi A, Kulkarni A, Feldman KW, Weiss A, McCourt EA, Schloff S, Partington M, Forbes B, Geddie BE, Bierbrauer K, Phillips PH, Rogers DL, Abed Alnabi W, Binenbaum G, Levin AV. Shi A, et al. Among authors: levin av. Pediatrics. 2019 Feb;143(2):e20181182. doi: 10.1542/peds.2018-1182. Epub 2019 Jan 10. Pediatrics. 2019. PMID: 30630868 Free PMC article.

4

Spectral-domain optical coherence tomography findings in Alström syndrome.

Dotan G, Khetan V, Marshall JD, Affel E, Armiger-George D, Naggert JK, Collin GB, Levin AV. Dotan G, et al. Among authors: levin av. Ophthalmic Genet. 2017 Sep-Oct;38(5):440-445. doi: 10.1080/13816810.2016.1257029. Epub 2017 Jan 23. Ophthalmic Genet. 2017. PMID: 28112973 Free PMC article.

5

Ocular anomalies in an infant with Klinefelter Syndrome.

Juhn AT, Nabi NU, Levin AV. Juhn AT, et al. Among authors: levin av. Ophthalmic Genet. 2012 Dec;33(4):232-4. doi: 10.3109/13816810.2012.670361. Epub 2012 Apr 9. Ophthalmic Genet. 2012. PMID: 22486321

6

Ophthalmic manifestations of Heimler syndrome due to PEX6 mutations.

Wangtiraumnuay N, Alnabi WA, Tsukikawa M, Thau A, Capasso J, Sharony R, Inglehearn CF, Levin AV. Wangtiraumnuay N, et al. Among authors: levin av. Ophthalmic Genet. 2018 Jun;39(3):384-390. doi: 10.1080/13816810.2018.1432063. Ophthalmic Genet. 2018. PMID: 29676688

7

Ethical considerations in gene therapy.

Levin AV. Levin AV. Ophthalmic Genet. 2016 Sep;37(3):249-51. doi: 10.3109/13816810.2015.1121501. Epub 2016 Feb 8. Ophthalmic Genet. 2016. PMID: 26854599 No abstract available.

8

Cornelia de Lange syndrome: parental preferences regarding the provision of medical information.

Hinkson DA, Atenafu E, Kennedy SJ, Vohra S, Garg D, Levin AV. Hinkson DA, et al. Among authors: levin av. Am J Med Genet A. 2006 Oct 15;140(20):2170-9. doi: 10.1002/ajmg.a.31404. Am J Med Genet A. 2006. PMID: 16906566

9

Paradoxical response to carbonic anhydrase inhibitors in patients with intraretinal cystoid spaces.

Guimaraes TAC, Capasso JE, Levin AV. Guimaraes TAC, et al. Among authors: levin av. Ophthalmic Genet. 2019 Jun;40(3):213-218. doi: 10.1080/13816810.2019.1622021. Epub 2019 Jul 2. Ophthalmic Genet. 2019. PMID: 31266384

10

Macular cystoid spaces in patients with retinal dystrophy.

Lingao MD, Ganesh A, Karthikeyan AS, Al Zuhaibi S, Al-Hosni A, Al Khayat A, Capasso J, Trumler AA, Stroh E, Al Shekaili H, Cater JR, Levin AV. Lingao MD, et al. Among authors: levin av. Ophthalmic Genet. 2016 Dec;37(4):377-383. doi: 10.3109/13816810.2015.1101775. Epub 2016 Feb 19. Ophthalmic Genet. 2016. PMID: 26894784

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