Héon E - Search Results

1

Correction: Gene therapy: perspectives from young adults with Leber's congenital amaurosis.

Napier MP, Selvan K, Hayeems RZ, Shuman C, Chitayat D, Sutherland JE, Day MA, Héon E. Napier MP, et al. Among authors: heon e. Eye (Lond). 2022 Nov;36(11):2228. doi: 10.1038/s41433-022-01994-8. Eye (Lond). 2022. PMID: 35217829 Free PMC article. No abstract available.

2

Natural history of Alström syndrome in early childhood: onset with dilated cardiomyopathy.

Michaud JL, Héon E, Guilbert F, Weill J, Puech B, Benson L, Smallhorn JF, Shuman CT, Buncic JR, Levin AV, Weksberg R, Brevière GM. Michaud JL, et al. Among authors: heon e. J Pediatr. 1996 Feb;128(2):225-9. doi: 10.1016/s0022-3476(96)70394-3. J Pediatr. 1996. PMID: 8636816

3

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: heon e. 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.

4

Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma.

Punnett A, Teshima I, Heon E, Budning A, Sutherland J, Gallie BL, Chan HS. Punnett A, et al. Among authors: heon e. Am J Med Genet A. 2003 Jul 1;120A(1):105-9. doi: 10.1002/ajmg.a.20116. Am J Med Genet A. 2003. PMID: 12794701

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: heon e. Can J Ophthalmol. 2006 Apr;41(2):190-6. doi: 10.1139/I06-007. Can J Ophthalmol. 2006. PMID: 16767206

6

Ocular Genetics Program: multidisciplinary care of patients with ocular genetic eye disease.

Morad Y, Sutherland J, DaSilva L, Ulster A, Shik J, Gallie B, Héon E, Levin AV. Morad Y, et al. Among authors: heon e. Can J Ophthalmol. 2007 Oct;42(5):734-8. doi: 10.3129/i07-144. Can J Ophthalmol. 2007. PMID: 17891201

7

Management and outcome of unilateral retinoblastoma.

Mallipatna AC, Sutherland JE, Gallie BL, Chan H, Héon E. Mallipatna AC, et al. Among authors: heon e. J AAPOS. 2009 Dec;13(6):546-50. doi: 10.1016/j.jaapos.2009.09.004. J AAPOS. 2009. PMID: 20006813

8

Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population.

Billingsley G, Bin J, Fieggen KJ, Duncan JL, Gerth C, Ogata K, Wodak SS, Traboulsi EI, Fishman GA, Paterson A, Chitayat D, Knueppel T, Millán JM, Mitchell GA, Deveault C, Héon E. Billingsley G, et al. Among authors: heon e. J Med Genet. 2010 Jul;47(7):453-63. doi: 10.1136/jmg.2009.073205. Epub 2010 May 14. J Med Genet. 2010. PMID: 20472660

9

Ultrasound biomicroscopy in the management of retinoblastoma.

Vasquez LM, Giuliari GP, Halliday W, Pavlin CJ, Gallie BL, Héon E. Vasquez LM, et al. Among authors: heon e. Eye (Lond). 2011 Feb;25(2):141-7. doi: 10.1038/eye.2010.193. Epub 2011 Jan 14. Eye (Lond). 2011. PMID: 21242989 Free PMC article.

10

BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition.

Deveault C, Billingsley G, Duncan JL, Bin J, Theal R, Vincent A, Fieggen KJ, Gerth C, Noordeh N, Traboulsi EI, Fishman GA, Chitayat D, Knueppel T, Millán JM, Munier FL, Kennedy D, Jacobson SG, Innes AM, Mitchell GA, Boycott K, Héon E. Deveault C, et al. Among authors: heon e. Hum Mutat. 2011 Jun;32(6):610-9. doi: 10.1002/humu.21480. Epub 2011 Mar 22. Hum Mutat. 2011. PMID: 21344540

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