Heon E - Search Results

1

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. Among authors: heon e. Mol Vis. 2006 May 16;12:506-10. Mol Vis. 2006. PMID: 16735991 Free article.

2

Peters' anomaly. The spectrum of associated ocular and systemic malformations.

Heon E, Barsoum-Homsy M, Cevrette L, Jacob JL, Milot J, Polemeno R, Musarella MA. Heon E, et al. Ophthalmic Paediatr Genet. 1992 Jun;13(2):137-43. doi: 10.3109/13816819209087614. Ophthalmic Paediatr Genet. 1992. PMID: 1495764

3

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

4

Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.

Fingert JH, Héon E, Liebmann JM, Yamamoto T, Craig JE, Rait J, Kawase K, Hoh ST, Buys YM, Dickinson J, Hockey RR, Williams-Lyn D, Trope G, Kitazawa Y, Ritch R, Mackey DA, Alward WL, Sheffield VC, Stone EM. Fingert JH, et al. Among authors: heon e. Hum Mol Genet. 1999 May;8(5):899-905. doi: 10.1093/hmg/8.5.899. Hum Mol Genet. 1999. PMID: 10196380

5

The gamma-crystallins and human cataracts: a puzzle made clearer.

Héon E, Priston M, Schorderet DF, Billingsley GD, Girard PO, Lubsen N, Munier FL. Héon E, et al. Am J Hum Genet. 1999 Nov;65(5):1261-7. doi: 10.1086/302619. Am J Hum Genet. 1999. PMID: 10521291 Free PMC article.

6

Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.

Gill D, Klose R, Munier FL, McFadden M, Priston M, Billingsley G, Ducrey N, Schorderet DF, Héon E. Gill D, et al. Among authors: heon e. Invest Ophthalmol Vis Sci. 2000 Jan;41(1):159-65. Invest Ophthalmol Vis Sci. 2000. PMID: 10634616

7

Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.

Mirzayans F, Gould DB, Héon E, Billingsley GD, Cheung JC, Mears AJ, Walter MA. Mirzayans F, et al. Among authors: heon e. Eur J Hum Genet. 2000 Jan;8(1):71-4. doi: 10.1038/sj.ejhg.5200354. Eur J Hum Genet. 2000. PMID: 10713890

8

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

9

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.

10

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

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