Hassinen IE - Search Results

1

Increased activities of antioxidant enzymes and decreased ATP concentration in cultured myoblasts with the 3243A-->G mutation in mitochondrial DNA.

Rusanen H, Majamaa K, Hassinen IE. Rusanen H, et al. Among authors: hassinen ie. Biochim Biophys Acta. 2000 Jan 3;1500(1):10-6. doi: 10.1016/s0925-4439(99)00081-2. Biochim Biophys Acta. 2000. PMID: 10564713 Free article.

2

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

Majamaa-Voltti K, Peuhkurinen K, Kortelainen ML, Hassinen IE, Majamaa K. Majamaa-Voltti K, et al. Among authors: hassinen ie. BMC Cardiovasc Disord. 2002 Aug 1;2:12. doi: 10.1186/1471-2261-2-12. BMC Cardiovasc Disord. 2002. PMID: 12150714 Free PMC article.

3

Cytoskeletal structure of myoblasts with the mitochondrial DNA 3243A-->G mutation and of osteosarcoma cells with respiratory chain deficiency.

Rusanen H, Annunen J, Ylä-Outinen H, Laurila A, Peltonen J, Hassinen IE, Majamaa K. Rusanen H, et al. Among authors: hassinen ie. Cell Motil Cytoskeleton. 2002 Nov;53(3):231-8. doi: 10.1002/cm.10066. Cell Motil Cytoskeleton. 2002. PMID: 12211104

4

LHON/MELAS overlap mutation in ND1 subunit of mitochondrial complex I affects ubiquinone binding as revealed by modeling in Escherichia coli NDH-1.

Pätsi J, Maliniemi P, Pakanen S, Hinttala R, Uusimaa J, Majamaa K, Nyström T, Kervinen M, Hassinen IE. Pätsi J, et al. Among authors: hassinen ie. Biochim Biophys Acta. 2012 Feb;1817(2):312-8. doi: 10.1016/j.bbabio.2011.10.014. Epub 2011 Nov 4. Biochim Biophys Acta. 2012. PMID: 22079202 Free article.

5

Myocardial glucose uptake in patients with the m.3243A > G mutation in mitochondrial DNA.

Lindroos MM, Pärkkä JP, Taittonen MT, Iozzo P, Kärppä M, Hassinen IE, Knuuti J, Nuutila P, Majamaa K. Lindroos MM, et al. Among authors: hassinen ie. J Inherit Metab Dis. 2016 Jan;39(1):67-74. doi: 10.1007/s10545-015-9865-1. Epub 2015 Jun 26. J Inherit Metab Dis. 2016. PMID: 26112752

6

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: hassinen ie. Neurology. 1995 Jun;45(6):1188-92. doi: 10.1212/wnl.45.6.1188. Neurology. 1995. PMID: 7783887

7

Increase of blood NAD+ and attenuation of lactacidemia during nicotinamide treatment of a patient with the MELAS syndrome.

Majamaa K, Rusanen H, Remes AM, Pyhtinen J, Hassinen IE. Majamaa K, et al. Among authors: hassinen ie. Life Sci. 1996;58(8):691-9. doi: 10.1016/s0024-3205(96)80008-7. Life Sci. 1996. PMID: 8594319

8

Metabolic interventions against complex I deficiency in MELAS syndrome.

Majamaa K, Rusanen H, Remes A, Hassinen IE. Majamaa K, et al. Among authors: hassinen ie. Mol Cell Biochem. 1997 Sep;174(1-2):291-6. Mol Cell Biochem. 1997. PMID: 9309702

9

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

10

Increased prevalence of vitiligo, but no evidence of premature ageing, in the skin of patients with bp 3243 mutation in mitochondrial DNA in the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome (MELAS).

Karvonen SL, Haapasaari KM, Kallioinen M, Oikarinen A, Hassinen IE, Majamaa K. Karvonen SL, et al. Among authors: hassinen ie. Br J Dermatol. 1999 Apr;140(4):634-9. doi: 10.1046/j.1365-2133.1999.02761.x. Br J Dermatol. 1999. PMID: 10233312

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