Riemslag FC - Search Results

1

A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

Assink JJ, Tijmes NT, ten Brink JB, Oostra RJ, Riemslag FC, de Jong PT, Bergen AA. Assink JJ, et al. Among authors: riemslag fc. Am J Hum Genet. 1997 Oct;61(4):934-9. doi: 10.1086/514884. Am J Hum Genet. 1997. PMID: 9382106 Free PMC article.

2

Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region.

Bergen AA, ten Brink JB, Riemslag F, Schuurman EJ, Tijmes N. Bergen AA, et al. Hum Mol Genet. 1995 May;4(5):931-5. doi: 10.1093/hmg/4.5.931. Hum Mol Genet. 1995. PMID: 7633454

3

Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

Bergen AA, ten Brink JB, Riemslag F, Schuurman EJ, Meire F, Tijmes N, de Jong PT. Bergen AA, et al. J Med Genet. 1996 Oct;33(10):869-72. doi: 10.1136/jmg.33.10.869. J Med Genet. 1996. PMID: 8933343 Free PMC article.

4

Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.

van den Born LI, van Schooneveld MJ, de Jong LA, Riemslag FC, de Jong PT, Gal A, Bleeker-Wagemakers EM. van den Born LI, et al. Among authors: riemslag fc. Ophthalmic Genet. 1994 Jun;15(2):51-60. doi: 10.3109/13816819409098864. Ophthalmic Genet. 1994. PMID: 7850269

5

Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epithelium.

van den Born LI, van Soest S, van Schooneveld MJ, Riemslag FC, de Jong PT, Bleeker-Wagemakers EM. van den Born LI, et al. Among authors: riemslag fc. Am J Ophthalmol. 1994 Oct 15;118(4):430-9. doi: 10.1016/s0002-9394(14)75792-7. Am J Ophthalmol. 1994. PMID: 7943119

6

Correspondence.

Boon CJ, van den Born LI, Keunen JE, Bergen AA, Riemslag FC, Florijn RJ, van Schooneveld MJ. Boon CJ, et al. Among authors: riemslag fc. Retina. 2015 Sep;35(9):e57-8. doi: 10.1097/IAE.0000000000000696. Retina. 2015. PMID: 26312452 No abstract available.

7

Clinical course of cone dystrophy caused by mutations in the RPGR gene.

Thiadens AA, Soerjoesing GG, Florijn RJ, Tjiam AG, den Hollander AI, van den Born LI, Riemslag FC, Bergen AA, Klaver CC. Thiadens AA, et al. Among authors: riemslag fc. Graefes Arch Clin Exp Ophthalmol. 2011 Oct;249(10):1527-35. doi: 10.1007/s00417-011-1789-3. Epub 2011 Aug 25. Graefes Arch Clin Exp Ophthalmol. 2011. PMID: 21866333 Free PMC article.

8

Autosomal recessive bestrophinopathy: differential diagnosis and treatment options.

Boon CJ, van den Born LI, Visser L, Keunen JE, Bergen AA, Booij JC, Riemslag FC, Florijn RJ, van Schooneveld MJ. Boon CJ, et al. Among authors: riemslag fc. Ophthalmology. 2013 Apr;120(4):809-20. doi: 10.1016/j.ophtha.2012.09.057. Epub 2013 Jan 3. Ophthalmology. 2013. PMID: 23290749

9

Cone-rod dystrophy can be a manifestation of Danon disease.

Thiadens AA, Slingerland NW, Florijn RJ, Visser GH, Riemslag FC, Klaver CC. Thiadens AA, et al. Among authors: riemslag fc. Graefes Arch Clin Exp Ophthalmol. 2012 May;250(5):769-74. doi: 10.1007/s00417-011-1857-8. Graefes Arch Clin Exp Ophthalmol. 2012. PMID: 22290069 Free PMC article.

10

The key role of electrophysiology in the diagnosis of visually impaired children.

van Genderen M, Riemslag F, Jorritsma F, Hoeben F, Meire F, Stilma J. van Genderen M, et al. Acta Ophthalmol Scand. 2006 Dec;84(6):799-806. doi: 10.1111/j.1600-0420.2006.00717.x. Acta Ophthalmol Scand. 2006. PMID: 17083542 Free article.

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