Heon E - Search Results

1

Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task Force.

Drack AV, Miraldi Utz V, Wang K, Alcorn DM, Brooks BP, Costakos DM, Couser NL, Heon E, Levin AV, Lloyd IC, Morse CL, Schmitt MA, Whitman MC, Traboulsi EI. Drack AV, et al. Among authors: heon e. J AAPOS. 2019 Aug;23(4):226-228.e1. doi: 10.1016/j.jaapos.2019.04.005. Epub 2019 Jun 21. J AAPOS. 2019. PMID: 31233830

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

Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS gene and apparent locus heterogeneity.

Oh J, Ho L, Ala-Mello S, Amato D, Armstrong L, Bellucci S, Carakushansky G, Ellis JP, Fong CT, Green JS, Heon E, Legius E, Levin AV, Nieuwenhuis HK, Pinckers A, Tamura N, Whiteford ML, Yamasaki H, Spritz RA. Oh J, et al. Among authors: heon e. Am J Hum Genet. 1998 Mar;62(3):593-8. doi: 10.1086/301757. Am J Hum Genet. 1998. PMID: 9497254 Free PMC article.

4

Mutation analysis of 3 genes in patients with Leber congenital amaurosis.

Lotery AJ, Namperumalsamy P, Jacobson SG, Weleber RG, Fishman GA, Musarella MA, Hoyt CS, Héon E, Levin A, Jan J, Lam B, Carr RE, Franklin A, Radha S, Andorf JL, Sheffield VC, Stone EM. Lotery AJ, et al. Among authors: heon e. Arch Ophthalmol. 2000 Apr;118(4):538-43. doi: 10.1001/archopht.118.4.538. Arch Ophthalmol. 2000. PMID: 10766140

5

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.

6

Ultrasound biomicroscopy of the eye in cystinosis.

Mungan N, Nischal KK, Héon E, MacKeen L, Balfe JW, Levin AV. Mungan N, et al. Among authors: heon e. Arch Ophthalmol. 2000 Oct;118(10):1329-33. doi: 10.1001/archopht.118.10.1329. Arch Ophthalmol. 2000. PMID: 11030813

7

Focal therapy in the management of retinoblastoma: when to start and when to stop.

Hamel P, Heon E, Gallie BL, Budning AS. Hamel P, et al. Among authors: heon e. J AAPOS. 2000 Dec;4(6):334-7. doi: 10.1067/mpa.2000.107902. J AAPOS. 2000. PMID: 11124666

8

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: heon e. Hum Mol Genet. 2001 Aug 1;10(16):1631-8. doi: 10.1093/hmg/10.16.1631. Hum Mol Genet. 2001. PMID: 11487566

9

Values of electroretinogram responses according to axial length.

Westall CA, Dhaliwal HS, Panton CM, Sigesmun D, Levin AV, Nischal KK, Héon E. Westall CA, et al. Among authors: heon e. Doc Ophthalmol. 2001 Mar;102(2):115-30. doi: 10.1023/a:1017535207481. Doc Ophthalmol. 2001. PMID: 11518455

10

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: heon e. 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.

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