Kärppä M - Search Results

1

Status epilepticus in POLG disease: a large multinational study.

Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Brodtkorb E, Ostergaard E, de Coo I, Pias-Peleteiro L, Isohanni P, Uusimaa J, Majamaa K, Kärppä M, Ortigoza-Escobar JD, Tangeraas T, Berland S, Harrison E, Biggs H, Horvath R, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. Among authors: karppa m. J Neurol. 2024 Aug;271(8):5156-5164. doi: 10.1007/s00415-024-12463-5. Epub 2024 Jun 1. J Neurol. 2024. PMID: 38822839 Free PMC article.

2

Vapinan erotusdiagnostiikka ja hoito.

Kärppä M. Kärppä M. Duodecim. 2007;123(2):161-8. Duodecim. 2007. PMID: 17328406 Finnish. No abstract available.

3

Impact of age and sex on the efficacy of fremanezumab in patients with difficult-to-treat migraine: results of the randomized, placebo-controlled, phase 3b FOCUS study.

MaassenVanDenBrink A, Terwindt GM, Cohen JM, Barash S, Campos VR, Galic M, Ning X, Kärppä M. MaassenVanDenBrink A, et al. Among authors: karppa m. J Headache Pain. 2021 Dec 18;22(1):152. doi: 10.1186/s10194-021-01336-1. J Headache Pain. 2021. PMID: 34922436 Free PMC article. Clinical Trial.

4

The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct.

Majamaa K, Turkka J, Kärppä M, Winqvist S, Hassinen IE. Majamaa K, et al. Among authors: karppa m. Neurology. 1997 Nov;49(5):1331-4. doi: 10.1212/wnl.49.5.1331. Neurology. 1997. PMID: 9371917

5

Peripheral neuropathy in patients with the 3243A>G mutation in mitochondrial DNA.

Kärppä M, Syrjälä P, Tolonen U, Majamaa K. Kärppä M, et al. J Neurol. 2003 Feb;250(2):216-21. doi: 10.1007/s00415-003-0981-8. J Neurol. 2003. PMID: 12574954 Clinical Trial.

6

A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like disease.

Uusimaa J, Finnilä S, Vainionpää L, Kärppä M, Herva R, Rantala H, Hassinen IE, Majamaa K. Uusimaa J, et al. Among authors: karppa m. Pediatrics. 2003 Mar;111(3):e262-8. doi: 10.1542/peds.111.3.e262. Pediatrics. 2003. PMID: 12612282

7

Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.

Kärppä M, Mahjneh I, Karttunen A, Tolonen U, Majamaa K. Kärppä M, et al. J Neurol. 2004 May;251(5):556-63. doi: 10.1007/s00415-004-0363-x. J Neurol. 2004. PMID: 15164188

8

Prevalence of large-scale mitochondrial DNA deletions in an adult Finnish population.

Remes AM, Majamaa-Voltti K, Kärppä M, Moilanen JS, Uimonen S, Helander H, Rusanen H, Salmela PI, Sorri M, Hassinen IE, Majamaa K. Remes AM, et al. Among authors: karppa m. Neurology. 2005 Mar 22;64(6):976-81. doi: 10.1212/01.WNL.0000154518.31302.ED. Neurology. 2005. PMID: 15781811

9

Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.

Kärppä M, Herva R, Moslemi AR, Oldfors A, Kakko S, Majamaa K. Kärppä M, et al. Brain. 2005 Aug;128(Pt 8):1861-9. doi: 10.1093/brain/awh515. Epub 2005 Apr 27. Brain. 2005. PMID: 15857931

10

A 3-year clinical follow-up of adult patients with 3243A>G in mitochondrial DNA.

Majamaa-Voltti KA, Winqvist S, Remes AM, Tolonen U, Pyhtinen J, Uimonen S, Kärppä M, Sorri M, Peuhkurinen K, Majamaa K. Majamaa-Voltti KA, et al. Among authors: karppa m. Neurology. 2006 May 23;66(10):1470-5. doi: 10.1212/01.wnl.0000216136.61640.79. Neurology. 2006. PMID: 16717204

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