Nikoskelainen E - Search Results

1

Neurological symptoms and natural course of xeroderma pigmentosum.

Anttinen A, Koulu L, Nikoskelainen E, Portin R, Kurki T, Erkinjuntti M, Jaspers NG, Raams A, Green MH, Lehmann AR, Wing JF, Arlett CF, Marttila RJ. Anttinen A, et al. Among authors: nikoskelainen e. Brain. 2008 Aug;131(Pt 8):1979-89. doi: 10.1093/brain/awn126. Epub 2008 Jun 21. Brain. 2008. PMID: 18567921 Free article.

2

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

Nikoskelainen EK, Marttila RJ, Huoponen K, Juvonen V, Lamminen T, Sonninen P, Savontaus ML. Nikoskelainen EK, et al. J Neurol Neurosurg Psychiatry. 1995 Aug;59(2):160-4. doi: 10.1136/jnnp.59.2.160. J Neurol Neurosurg Psychiatry. 1995. PMID: 7629530 Free PMC article.

3

Familial olivopontocerebellar atrophy with macular degeneration: a separate entity among the olivopontocerebellar atrophies.

Anttinen A, Nikoskelainen E, Marttila RJ, Grenman R, Falck B, Aarnisalo E, Kalimo H. Anttinen A, et al. Among authors: nikoskelainen e. Acta Neurol Scand. 1986 Feb;73(2):180-90. doi: 10.1111/j.1600-0404.1986.tb03261.x. Acta Neurol Scand. 1986. PMID: 3705927

4

[Olfactory nerve meningioma].

Tani P, Nikoskelainen E, Marttila R. Tani P, et al. Among authors: nikoskelainen e. Duodecim. 1987;103(13):810-6. Duodecim. 1987. PMID: 3665778 Finnish. No abstract available.

5

[Rare extrapyramidal disorders: progressive supranuclear paralysis and striato-nigral degeneration].

Marttila R, Kalimo H, Nikoskelainen E, Rinne UK. Marttila R, et al. Among authors: nikoskelainen e. Duodecim. 1982;98(3):191-200. Duodecim. 1982. PMID: 7060514 Finnish. No abstract available.

6

Vigabatrin, a gabaergic antiepileptic drug, causes concentric visual field defects.

Kälviäinen R, Nousiainen I, Mäntyjärvi M, Nikoskelainen E, Partanen J, Partanen K, Riekkinen P Sr. Kälviäinen R, et al. Among authors: nikoskelainen e. Neurology. 1999 Sep 22;53(5):922-6. doi: 10.1212/wnl.53.5.922. Neurology. 1999. PMID: 10496247 Clinical Trial.

7

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

8

Pre-excitation syndrome in Leber's hereditary optic neuropathy.

Nikoskelainen EK, Savontaus ML, Huoponen K, Antila K, Hartiala J. Nikoskelainen EK, et al. Lancet. 1994 Sep 24;344(8926):857-8. doi: 10.1016/s0140-6736(94)92830-4. Lancet. 1994. PMID: 7916404

9

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.

10

Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism.

Vilkki J, Savontaus ML, Nikoskelainen EK. Vilkki J, et al. Among authors: nikoskelainen ek. Am J Hum Genet. 1989 Aug;45(2):206-11. Am J Hum Genet. 1989. PMID: 2757028 Free PMC article.

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