Levin AV - Search Results

1

Molecular characterisation of congenital glaucoma in a consanguineous Canadian community: a step towards preventing glaucoma related blindness.

Martin SN, Sutherland J, Levin AV, Klose R, Priston M, Héon E. Martin SN, et al. Among authors: levin av. J Med Genet. 2000 Jun;37(6):422-7. doi: 10.1136/jmg.37.6.422. J Med Genet. 2000. PMID: 10851252 Free PMC article.

2

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene.

Vincent AL, Billingsley G, Buys Y, Levin AV, Priston M, Trope G, Williams-Lyn D, Héon E. Vincent AL, et al. Among authors: levin av. Am J Hum Genet. 2002 Feb;70(2):448-60. doi: 10.1086/338709. Epub 2002 Jan 3. Am J Hum Genet. 2002. PMID: 11774072 Free PMC article.

3

Further support of the role of CYP1B1 in patients with Peters anomaly.

Vincent A, Billingsley G, Priston M, Glaser T, Oliver E, Walter M, Ritch R, Levin A, Heon E. Vincent A, et al. Mol Vis. 2006 May 16;12:506-10. Mol Vis. 2006. PMID: 16735991 Free article.

4

Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly.

Vincent A, Billingsley G, Priston M, Williams-Lyn D, Sutherland J, Glaser T, Oliver E, Walter MA, Heathcote G, Levin A, Héon E. Vincent A, et al. J Med Genet. 2001 May;38(5):324-6. doi: 10.1136/jmg.38.5.324. J Med Genet. 2001. PMID: 11403040 Free PMC article. No abstract available.

5

Utility of molecular testing for related retinal dystrophies.

Mezer E, Sutherland J, Goei SL, Héon E, Levin AV. Mezer E, et al. Among authors: levin av. Can J Ophthalmol. 2006 Apr;41(2):190-6. doi: 10.1139/I06-007. Can J Ophthalmol. 2006. PMID: 16767206

6

Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome.

Priston M, Kozlowski K, Gill D, Letwin K, Buys Y, Levin AV, Walter MA, Héon E. Priston M, et al. Among authors: levin av. Hum Mol Genet. 2001 Aug 1;10(16):1631-8. doi: 10.1093/hmg/10.16.1631. Hum Mol Genet. 2001. PMID: 11487566

7

In memoriam Maria Musarella.

Héon E, Levin A, MacDonald IM. Héon E, et al. Ophthalmic Genet. 2014 Sep;35(3):129. doi: 10.3109/13816810.2014.907922. Epub 2014 Apr 21. Ophthalmic Genet. 2014. PMID: 24749744 No abstract available.

8

Defining the pathogenicity of optineurin in juvenile open-angle glaucoma.

Willoughby CE, Chan LL, Herd S, Billingsley G, Noordeh N, Levin AV, Buys Y, Trope G, Sarfarazi M, Héon E. Willoughby CE, et al. Among authors: levin av. Invest Ophthalmol Vis Sci. 2004 Sep;45(9):3122-30. doi: 10.1167/iovs.04-0107. Invest Ophthalmol Vis Sci. 2004. PMID: 15326130

9

Eight previously unidentified mutations found in the OA1 ocular albinism gene.

Mayeur H, Roche O, Vêtu C, Jaliffa C, Marchant D, Dollfus H, Bonneau D, Munier FL, Schorderet DF, Levin AV, Héon E, Sutherland J, Lacombe D, Said E, Mezer E, Kaplan J, Dufier JL, Marsac C, Menasche M, Abitbol M. Mayeur H, et al. Among authors: levin av. BMC Med Genet. 2006 Apr 28;7:41. doi: 10.1186/1471-2350-7-41. BMC Med Genet. 2006. PMID: 16646960 Free PMC article.

10

Mutational analysis of the OA1 gene in ocular albinism.

Camand O, Boutboul S, Arbogast L, Roche O, Sternberg C, Sutherland J, Levin A, Héon E, Menasche M, Dufier J, Abitbol M. Camand O, et al. Ophthalmic Genet. 2003 Sep;24(3):167-73. doi: 10.1076/opge.24.3.167.15605. Ophthalmic Genet. 2003. PMID: 12868035

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