Casteels I - Search Results

1

Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutations.

Cassiman C, Spileers W, De Baere E, de Ravel T, Casteels I. Cassiman C, et al. Among authors: casteels i. Ophthalmic Genet. 2013 Mar-Jun;34(1-2):105-8. doi: 10.3109/13816810.2012.726395. Epub 2012 Oct 5. Ophthalmic Genet. 2013. PMID: 23039133

2

Mucolipidosis type IV. Presentation of a mild variant.

Casteels I, Taylor DS, Lake BD, Spalton DJ, Bach G. Casteels I, et al. Ophthalmic Paediatr Genet. 1992 Dec;13(4):205-10. doi: 10.3109/13816819209105168. Ophthalmic Paediatr Genet. 1992. PMID: 1488220

3

Leber congenital amaurosis and Lhermitte-Duclos syndrome: a previously unreported association.

Casteels I, Demaerel P, De Cock P, Casaer P, Spileers W, Wilms G. Casteels I, et al. J Pediatr Ophthalmol Strabismus. 1995 Mar-Apr;32(2):117-9. doi: 10.3928/0191-3913-19950301-13. J Pediatr Ophthalmol Strabismus. 1995. PMID: 7629666 No abstract available.

4

Optic atrophy as the presenting sign in Hallervorden-Spatz syndrome.

Casteels I, Spileers W, Swinnen T, Demaerel P, Silberstein J, Casaer P, Missotten L. Casteels I, et al. Neuropediatrics. 1994 Oct;25(5):265-7. doi: 10.1055/s-2008-1073034. Neuropediatrics. 1994. PMID: 7885538

5

Leber congenital amaurosis--differential diagnosis, ophthalmological and neuroradiological report of 18 patients.

Casteels I, Spileers W, Demaerel P, Casaer P, De Cock P, Dralands L, Missotten L. Casteels I, et al. Neuropediatrics. 1996 Aug;27(4):189-93. doi: 10.1055/s-2007-973785. Neuropediatrics. 1996. PMID: 8892367

6

Evolution of ophthalmic and electrophysiological findings in identical twin sisters with the carbohydrate deficient glycoprotein syndrome type 1 over a period of 14 years.

Casteels I, Spileers W, Leys A, Lagae L, Jaeken J. Casteels I, et al. Br J Ophthalmol. 1996 Oct;80(10):900-2. doi: 10.1136/bjo.80.10.900. Br J Ophthalmol. 1996. PMID: 8976701 Free PMC article.

7

Cortical visual impairment following perinatal hypoxia: clinicoradiologic correlation using magnetic resonance imaging.

Casteels I, Demaerel P, Spileers W, Lagae L, Missotten L, Casaer P. Casteels I, et al. J Pediatr Ophthalmol Strabismus. 1997 Sep-Oct;34(5):297-305. doi: 10.3928/0191-3913-19970901-09. J Pediatr Ophthalmol Strabismus. 1997. PMID: 9310919

8

The baby with poor visual contact.

Casteels I, Spileers W, Missotten L, Casaer P. Casteels I, et al. Br J Ophthalmol. 1998 Nov;82(11):1228-9. doi: 10.1136/bjo.82.11.1228. Br J Ophthalmol. 1998. PMID: 9924322 Free PMC article. No abstract available.

9

Microarray-based mutation detection and phenotypic characterization of patients with Leber congenital amaurosis.

Yzer S, Leroy BP, De Baere E, de Ravel TJ, Zonneveld MN, Voesenek K, Kellner U, Ciriano JP, de Faber JT, Rohrschneider K, Roepman R, den Hollander AI, Cruysberg JR, Meire F, Casteels I, van Moll-Ramirez NG, Allikmets R, van den Born LI, Cremers FP. Yzer S, et al. Among authors: casteels i. Invest Ophthalmol Vis Sci. 2006 Mar;47(3):1167-76. doi: 10.1167/iovs.05-0848. Invest Ophthalmol Vis Sci. 2006. PMID: 16505055 Free article.

10

Literature review on preschool vision screening.

Cools G, Houtman AC, Spileers W, Van Kerschaver E, Casteels I. Cools G, et al. Among authors: casteels i. Bull Soc Belge Ophtalmol. 2009;(313):49-63. Bull Soc Belge Ophtalmol. 2009. PMID: 20108573 Review.

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