Rusanen H - Search Results

1

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. Cell Motil Cytoskeleton. 2002 Nov;53(3):231-8. doi: 10.1002/cm.10066. Cell Motil Cytoskeleton. 2002. PMID: 12211104

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

3

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: rusanen h. Life Sci. 1996;58(8):691-9. doi: 10.1016/s0024-3205(96)80008-7. Life Sci. 1996. PMID: 8594319

4

Metabolic interventions against complex I deficiency in MELAS syndrome.

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

5

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

Majamaa K, Moilanen JS, Uimonen S, Remes AM, Salmela PI, Kärppä M, Majamaa-Voltti KA, Rusanen H, Sorri M, Peuhkurinen KJ, Hassinen IE. Majamaa K, et al. Among authors: rusanen h. Am J Hum Genet. 1998 Aug;63(2):447-54. doi: 10.1086/301959. Am J Hum Genet. 1998. PMID: 9683591 Free PMC article.

6

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. 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.

7

Epidemiology of the mitochondrial DNA 8344A>G mutation for the myoclonus epilepsy and ragged red fibres (MERRF) syndrome.

Remes AM, Kärppä M, Moilanen JS, Rusanen H, Hassinen IE, Majamaa K, Uimonen S, Sorri M, Salmela PI, Karvonen SL, Karvonen SL. Remes AM, et al. Among authors: rusanen h. J Neurol Neurosurg Psychiatry. 2003 Aug;74(8):1158-9. doi: 10.1136/jnnp.74.8.1158. J Neurol Neurosurg Psychiatry. 2003. PMID: 12876264 Free PMC article. No abstract available.

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: rusanen h. Neurology. 2005 Mar 22;64(6):976-81. doi: 10.1212/01.WNL.0000154518.31302.ED. Neurology. 2005. PMID: 15781811

9

A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic hypogonadism.

Kytövuori L, Lipponen J, Rusanen H, Komulainen T, Martikainen MH, Majamaa K. Kytövuori L, et al. Among authors: rusanen h. J Neurol. 2016 Nov;263(11):2188-2195. doi: 10.1007/s00415-016-8249-2. Epub 2016 Aug 8. J Neurol. 2016. PMID: 27502083

10

Molecular epidemiology of hereditary ataxia in Finland.

Lipponen J, Helisalmi S, Raivo J, Siitonen A, Doi H, Rusanen H, Lehtilahti M, Ryytty M, Laakso M, Tanaka F, Majamaa K, Kytövuori L. Lipponen J, et al. Among authors: rusanen h. BMC Neurol. 2021 Oct 2;21(1):382. doi: 10.1186/s12883-021-02409-z. BMC Neurol. 2021. PMID: 34600502 Free PMC article.

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