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Year | Number of Results |
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1989 | 1 |
1990 | 1 |
1991 | 1 |
1994 | 1 |
1998 | 2 |
2007 | 1 |
2024 | 0 |
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Page 1
Familial vascular retinopathy. A preliminary report.
Doc Ophthalmol. 1990 Oct;75(3-4):259-61. doi: 10.1007/BF00164839.
Doc Ophthalmol. 1990.
PMID: 2090400
A new autosomal dominant vascular retinopathy syndrome.
Storimans CW, Van Schooneveld MJ, Oosterhuis JA, Bos PJ.
Storimans CW, et al.
Eur J Ophthalmol. 1991 Apr-Jun;1(2):73-8. doi: 10.1177/112067219100100204.
Eur J Ophthalmol. 1991.
PMID: 1821204
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C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy.
Richards A, van den Maagdenberg AM, Jen JC, Kavanagh D, Bertram P, Spitzer D, Liszewski MK, Barilla-Labarca ML, Terwindt GM, Kasai Y, McLellan M, Grand MG, Vanmolkot KR, de Vries B, Wan J, Kane MJ, Mamsa H, Schäfer R, Stam AH, Haan J, de Jong PT, Storimans CW, van Schooneveld MJ, Oosterhuis JA, Gschwendter A, Dichgans M, Kotschet KE, Hodgkinson S, Hardy TA, Delatycki MB, Hajj-Ali RA, Kothari PH, Nelson SF, Frants RR, Baloh RW, Ferrari MD, Atkinson JP.
Richards A, et al. Among authors: storimans cw.
Nat Genet. 2007 Sep;39(9):1068-70. doi: 10.1038/ng2082. Epub 2007 Jul 29.
Nat Genet. 2007.
PMID: 17660820
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Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.
Terwindt GM, Haan J, Ophoff RA, Groenen SM, Storimans CW, Lanser JB, Roos RA, Bleeker-Wagemakers EM, Frants RR, Ferrari MD.
Terwindt GM, et al. Among authors: storimans cw.
Brain. 1998 Feb;121 ( Pt 2):303-16. doi: 10.1093/brain/121.2.303.
Brain. 1998.
PMID: 9549508
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Serotoninergic status in patients with hereditary vascular retinopathy syndrome.
Storimans CW, Fekkes D, van Dalen A, Bleeker-Wagemakers ED, Oosterhuis JA.
Storimans CW, et al.
Br J Ophthalmol. 1998 Aug;82(8):897-900. doi: 10.1136/bjo.82.8.897.
Br J Ophthalmol. 1998.
PMID: 9828773
Free PMC article.
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[With an eye on... the champagne cork].
Keunen JE, Storimans CW.
Keunen JE, et al. Among authors: storimans cw.
Ned Tijdschr Geneeskd. 1994 Dec 24;138(52):2594-6.
Ned Tijdschr Geneeskd. 1994.
PMID: 7808531
Dutch.
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Rieger's eye anomaly and persistent hyperplastic primary vitreous.
Storimans CW, Van Schooneveld MJ.
Storimans CW, et al.
Ophthalmic Paediatr Genet. 1989 Dec;10(4):257-62. doi: 10.3109/13816818909009880.
Ophthalmic Paediatr Genet. 1989.
PMID: 2628817
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