Launes J - Search Results

1

Assessment of a DJ-1 (PARK7) polymorphism in Finnish PD.

Eerola J, Hernandez D, Launes J, Hellström O, Hague S, Gulick C, Johnson J, Peuralinna T, Hardy J, Tienari PJ, Singleton AB. Eerola J, et al. Among authors: launes j. Neurology. 2003 Oct 14;61(7):1000-2. doi: 10.1212/01.wnl.0000083992.28066.7e. Neurology. 2003. PMID: 14557580

2

Subcortical type cognitive impairment in herpes zoster encephalitis.

Hokkanen L, Launes J, Poutiainen E, Valanne L, Salonen O, Sirén J, Iivanainen M. Hokkanen L, et al. Among authors: launes j. J Neurol. 1997 Apr;244(4):239-45. doi: 10.1007/s004150050078. J Neurol. 1997. PMID: 9112592

3

Unilateral hyperfusion in brain-perfusion SPECT predicts poor prognosis in acute encephalitis.

Launes J, Sirén J, Valanne L, Salonen O, Nikkinen P, Seppäläinen AM, Liewendahl K. Launes J, et al. Neurology. 1997 May;48(5):1347-51. doi: 10.1212/wnl.48.5.1347. Neurology. 1997. PMID: 9153471

4

Release of soluble ICAM-5, a neuronal adhesion molecule, in acute encephalitis.

Lindsberg PJ, Launes J, Tian L, Välimaa H, Subramanian V, Sirén J, Hokkanen L, Hyypiä T, Carpén O, Gahmberg CG. Lindsberg PJ, et al. Among authors: launes j. Neurology. 2002 Feb 12;58(3):446-51. doi: 10.1212/wnl.58.3.446. Neurology. 2002. PMID: 11839847

5

Apolipoprotein E (APOE), PARKIN and catechol-O-methyltransferase (COMT) genes and susceptibility to sporadic Parkinson's disease in Finland.

Eerola J, Launes J, Hellström O, Tienari PJ. Eerola J, et al. Among authors: launes j. Neurosci Lett. 2002 Sep 27;330(3):296-8. doi: 10.1016/s0304-3940(02)00819-4. Neurosci Lett. 2002. PMID: 12270650

6

How useful is [123I]beta-CIT SPECT in clinical practice?

Eerola J, Tienari PJ, Kaakkola S, Nikkinen P, Launes J. Eerola J, et al. Among authors: launes j. J Neurol Neurosurg Psychiatry. 2005 Sep;76(9):1211-6. doi: 10.1136/jnnp.2004.045237. J Neurol Neurosurg Psychiatry. 2005. PMID: 16107353 Free PMC article. Clinical Trial.

7

Attrition in a 30-year follow-up of a perinatal birth risk cohort: factors change with age.

Launes J, Hokkanen L, Laasonen M, Tuulio-Henriksson A, Virta M, Lipsanen J, Tienari PJ, Michelsson K. Launes J, et al. PeerJ. 2014 Jul 8;2:e480. doi: 10.7717/peerj.480. eCollection 2014. PeerJ. 2014. PMID: 25071998 Free PMC article.

8

Carriership of two copies of C9orf72 hexanucleotide repeat intermediate-length alleles is a risk factor for ALS in the Finnish population.

Kaivola K, Salmi SJ, Jansson L, Launes J, Hokkanen L, Niemi AK, Majamaa K, Lahti J, Eriksson JG, Strandberg T, Laaksovirta H, Tienari PJ. Kaivola K, et al. Among authors: launes j. Acta Neuropathol Commun. 2020 Nov 9;8(1):187. doi: 10.1186/s40478-020-01059-5. Acta Neuropathol Commun. 2020. PMID: 33168078 Free PMC article.

9

ALS in Finland: Major Genetic Variants and Clinical Characteristics of Patients With and Without the C9orf72 Hexanucleotide Repeat Expansion.

Laaksovirta H, Launes J, Jansson L, Traynor BJ, Kaivola K, Tienari PJ. Laaksovirta H, et al. Among authors: launes j. Neurol Genet. 2022 Mar 14;8(2):e665. doi: 10.1212/NXG.0000000000000665. eCollection 2022 Apr. Neurol Genet. 2022. PMID: 35295181 Free PMC article.

10

C9orf72 hexanucleotide repeat allele tagging SNPs: Associations with ALS risk and longevity.

Kaivola K, Pirinen M, Laaksovirta H, Jansson L, Rautila O, Launes J, Hokkanen L, Lahti J, Eriksson JG, Strandberg TE, FinnGen, Tienari PJ. Kaivola K, et al. Among authors: launes j. Front Genet. 2023 Mar 1;14:1087098. doi: 10.3389/fgene.2023.1087098. eCollection 2023. Front Genet. 2023. PMID: 36936421 Free PMC article.

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