Héon E - Search Results

1

Ocular manifestations of the Johanson-Blizzard syndrome.

Cheung JC, Thomson H, Buncic JR, Héon E, Levin AV. Cheung JC, et al. Among authors: heon e. J AAPOS. 2009 Oct;13(5):512-4. doi: 10.1016/j.jaapos.2009.05.005. Epub 2009 Aug 29. J AAPOS. 2009. PMID: 19717322 Review.

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

The genetics of glaucoma: an update.

Liu S, Cheung JC, Héon E. Liu S, et al. Among authors: heon e. Can J Ophthalmol. 1997 Jun;32(4):221-8. Can J Ophthalmol. 1997. PMID: 9199828 Review. No abstract available.

4

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

5

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

6

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

7

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.

8

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

9

Mutations in the CRB1 gene cause Leber congenital amaurosis.

Lotery AJ, Jacobson SG, Fishman GA, Weleber RG, Fulton AB, Namperumalsamy P, Héon E, Levin AV, Grover S, Rosenow JR, Kopp KK, Sheffield VC, Stone EM. Lotery AJ, et al. Among authors: heon e. Arch Ophthalmol. 2001 Mar;119(3):415-20. doi: 10.1001/archopht.119.3.415. Arch Ophthalmol. 2001. PMID: 11231775

10

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

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