Majamaa K - Search Results

1

Cerebral oxygen and glucose metabolism in patients with mitochondrial m.3243A>G mutation.

Lindroos MM, Borra RJ, Parkkola R, Virtanen SM, Lepomäki V, Bucci M, Virta JR, Rinne JO, Nuutila P, Majamaa K. Lindroos MM, et al. Among authors: majamaa k. Brain. 2009 Dec;132(Pt 12):3274-84. doi: 10.1093/brain/awp259. Brain. 2009. PMID: 19843652

2

Demyelinating polyneuropathy in a patient with the tRNA(Leu)(UUR) mutation at base pair 3243 of the mitochondrial DNA.

Rusanen H, Majamaa K, Tolonen U, Remes AM, Myllylä R, Hassinen IE. Rusanen H, et al. Among authors: majamaa k. Neurology. 1995 Jun;45(6):1188-92. doi: 10.1212/wnl.45.6.1188. Neurology. 1995. PMID: 7783887

3

Adult-onset diabetes mellitus and neurosensory hearing loss in maternal relatives of MELAS patients in a family with the tRNA(Leu(UUR)) mutation.

Remes AM, Majamaa K, Herva R, Hassinen IE. Remes AM, et al. Among authors: majamaa k. Neurology. 1993 May;43(5):1015-20. doi: 10.1212/wnl.43.5.1015. Neurology. 1993. PMID: 8492919

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. Neurology. 1997 Nov;49(5):1331-4. doi: 10.1212/wnl.49.5.1331. Neurology. 1997. PMID: 9371917

5

Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G.

Moilanen JS, Majamaa K. Moilanen JS, et al. Among authors: majamaa k. Eur J Hum Genet. 2001 Jan;9(1):59-62. doi: 10.1038/sj.ejhg.5200550. Eur J Hum Genet. 2001. PMID: 11175302

6

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

Uimonen S, Moilanen JS, Sorri M, Hassinen IE, Majamaa K. Uimonen S, et al. Among authors: majamaa k. Hum Genet. 2001 Apr;108(4):284-9. doi: 10.1007/s004390100475. Hum Genet. 2001. PMID: 11379873

7

Ubiquinone and nicotinamide treatment of patients with the 3243A-->G mtDNA mutation.

Remes AM, Liimatta EV, Winqvist S, Tolonen U, Ranua JA, Reinikainen K, Hassinen IE, Majamaa K. Remes AM, et al. Among authors: majamaa k. Neurology. 2002 Oct 22;59(8):1275-7. doi: 10.1212/wnl.59.8.1275. Neurology. 2002. PMID: 12391367 Clinical Trial.

8

Pigmentary retinopathy in patients with the MELAS mutation 3243A-->G in mitochondrial DNA.

Latvala T, Mustonen E, Uusitalo R, Majamaa K. Latvala T, et al. Among authors: majamaa k. Graefes Arch Clin Exp Ophthalmol. 2002 Oct;240(10):795-801. doi: 10.1007/s00417-002-0555-y. Epub 2002 Sep 21. Graefes Arch Clin Exp Ophthalmol. 2002. PMID: 12397426

9

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

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

10

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. Among authors: majamaa k. J Neurol. 2004 May;251(5):556-63. doi: 10.1007/s00415-004-0363-x. J Neurol. 2004. PMID: 15164188

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