Héon E - Search Results

1

A modified protocol for the assessment of visual function in patients with retinitis pigmentosa.

Lodha N, Westall CA, Brent M, Abdolell M, Héon E. Lodha N, et al. Among authors: heon e. Adv Exp Med Biol. 2003;533:49-57. doi: 10.1007/978-1-4615-0067-4_7. Adv Exp Med Biol. 2003. PMID: 15180247

2

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

Sigesmund DA, Weleber RG, Pillers DA, Westall CA, Panton CM, Powell BR, Héon E, Murphey WH, Musarella MA, Ray PN. Sigesmund DA, et al. Among authors: heon e. Ophthalmology. 1994 May;101(5):856-65. doi: 10.1016/s0161-6420(13)31249-4. Ophthalmology. 1994. PMID: 8190471

3

Visual prognosis of Coats' disease.

Budning AS, Heon E, Gallie BL. Budning AS, et al. Among authors: heon e. J AAPOS. 1998 Dec;2(6):356-9. doi: 10.1016/s1091-8531(98)90034-9. J AAPOS. 1998. PMID: 10532724

4

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

5

Sleep and daytime sleepiness in retinitis pigmentosa patients.

Ionescu D, Driver HS, Heon E, Flanagan J, Shapiro CM. Ionescu D, et al. Among authors: heon e. J Sleep Res. 2001 Dec;10(4):329-35. doi: 10.1046/j.1365-2869.2001.00271.x. J Sleep Res. 2001. PMID: 11903863

6

Visual results in children treated for macular retinoblastoma.

Watts P, Westall C, Colpa L, MacKeen L, Abdolell M, Gallie B, Héon E. Watts P, et al. Among authors: heon e. Eye (Lond). 2002 Jan;16(1):75-80. doi: 10.1038/sj.eye.6700070. Eye (Lond). 2002. PMID: 11913894

7

VSX1: a gene for posterior polymorphous dystrophy and keratoconus.

Héon E, Greenberg A, Kopp KK, Rootman D, Vincent AL, Billingsley G, Priston M, Dorval KM, Chow RL, McInnes RR, Heathcote G, Westall C, Sutphin JE, Semina E, Bremner R, Stone EM. Héon E, et al. Hum Mol Genet. 2002 May 1;11(9):1029-36. doi: 10.1093/hmg/11.9.1029. Hum Mol Genet. 2002. PMID: 11978762

8

Pontocerebellar hypoplasia type 1: new leads for an earlier diagnosis.

Salman MS, Blaser S, Buncic JR, Westall CA, Héon E, Becker L. Salman MS, et al. Among authors: heon e. J Child Neurol. 2003 Mar;18(3):220-5. doi: 10.1177/08830738030180031201. J Child Neurol. 2003. PMID: 12731647

9

Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome.

Héon E, Westall C, Carmi R, Elbedour K, Panton C, Mackeen L, Stone EM, Sheffield VC. Héon E, et al. Am J Med Genet A. 2005 Jan 30;132A(3):283-7. doi: 10.1002/ajmg.a.30466. Am J Med Genet A. 2005. PMID: 15690372

10

Assessment of central retinal function in patients with advanced retinitis pigmentosa.

Gerth C, Wright T, Héon E, Westall CA. Gerth C, et al. Among authors: heon e. Invest Ophthalmol Vis Sci. 2007 Mar;48(3):1312-8. doi: 10.1167/iovs.06-0630. Invest Ophthalmol Vis Sci. 2007. PMID: 17325178

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