Nikoskelainen E - Search Results

1

Ophthalmologic findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a cross-sectional study.

Roine S, Harju M, Kivelä TT, Pöyhönen M, Nikoskelainen E, Tuisku S, Kalimo H, Viitanen M, Summanen PA. Roine S, et al. Among authors: nikoskelainen e. Ophthalmology. 2006 Aug;113(8):1411-7. doi: 10.1016/j.ophtha.2006.03.030. Ophthalmology. 2006. PMID: 16877080

2

Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.

Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H. Tyni T, et al. Among authors: nikoskelainen e. Ophthalmology. 1998 May;105(5):810-24. doi: 10.1016/S0161-6420(98)95019-9. Ophthalmology. 1998. PMID: 9593380

3

Scanning laser Doppler flowmetry shows reduced retinal capillary blood flow in CADASIL.

Harju M, Tuominen S, Summanen P, Viitanen M, Pöyhönen M, Nikoskelainen E, Kalimo H, Kivelä T. Harju M, et al. Among authors: nikoskelainen e. Stroke. 2004 Nov;35(11):2449-52. doi: 10.1161/01.STR.0000145048.94499.b9. Epub 2004 Oct 7. Stroke. 2004. PMID: 15472092

4

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations.

Nikoskelainen EK, Huoponen K, Juvonen V, Lamminen T, Nummelin K, Savontaus ML. Nikoskelainen EK, et al. Ophthalmology. 1996 Mar;103(3):504-14. doi: 10.1016/s0161-6420(96)30665-9. Ophthalmology. 1996. PMID: 8600429

5

Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy.

Vilkki J, Savontaus ML, Kalimo H, Nikoskelainen EK. Vilkki J, et al. Among authors: nikoskelainen ek. Hum Genet. 1989 Jun;82(3):208-12. doi: 10.1007/BF00291155. Hum Genet. 1989. PMID: 2567271

6

Ophthalmologic heterogeneity in subjects with gyrate atrophy of choroid and retina harboring the L402P mutation of ornithine aminotransferase.

Peltola KE, Näntö-Salonen K, Heinonen OJ, Jääskeläinen S, Heinänen K, Simell O, Nikoskelainen E. Peltola KE, et al. Among authors: nikoskelainen e. Ophthalmology. 2001 Apr;108(4):721-9. doi: 10.1016/s0161-6420(00)00587-x. Ophthalmology. 2001. PMID: 11297489

7

[Subacute necrotizing encephalomyelopathy (Leigh's disease)].

Kalimo H, Nikoskelainen E, Molnár G. Kalimo H, et al. Among authors: nikoskelainen e. Duodecim. 1980;96(16):1075-84. Duodecim. 1980. PMID: 7227232 Finnish. No abstract available.

8

Dominant optic atrophy: correlation between clinical and molecular genetic studies.

Puomila A, Huoponen K, Mäntyjärvi M, Hämäläinen P, Paananen R, Sankila EM, Savontaus ML, Somer M, Nikoskelainen E. Puomila A, et al. Among authors: nikoskelainen e. Acta Ophthalmol Scand. 2005 Jun;83(3):337-46. doi: 10.1111/j.1600-0420.2005.00448.x. Acta Ophthalmol Scand. 2005. PMID: 15948788 Free article.

9

Does sporadic Leber's disease exist?

Nikoskelainen E, Nummelin K, Savontaus ML. Nikoskelainen E, et al. J Clin Neuroophthalmol. 1988 Dec;8(4):225-9. J Clin Neuroophthalmol. 1988. PMID: 2977137

10

Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

Nikoskelainen E, Hassinen IE, Paljärvi L, Lang H, Kalimo H. Nikoskelainen E, et al. Lancet. 1984 Dec 22;2(8417-8418):1474. doi: 10.1016/s0140-6736(84)91669-6. Lancet. 1984. PMID: 6151084 No abstract available.

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