Suomalainen A - Search Results

1

Decrease of 3243 A-->G mtDNA mutation from blood in MELAS syndrome: a longitudinal study.

Rahman S, Poulton J, Marchington D, Suomalainen A. Rahman S, et al. Among authors: suomalainen a. Am J Hum Genet. 2001 Jan;68(1):238-40. doi: 10.1086/316930. Epub 2000 Nov 20. Am J Hum Genet. 2001. PMID: 11085913 Free PMC article.

2

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: suomalainen a. J Neurol. 1995 May;242(5):304-12. doi: 10.1007/BF00878873. J Neurol. 1995. PMID: 7643139

3

Quantification of mitochondrial DNA carrying the tRNA(8344Lys) point mutation in myoclonus epilepsy and ragged-red-fiber disease.

Suomalainen A, Kollmann P, Octave JN, Söderlund H, Syvänen AC. Suomalainen A, et al. Eur J Hum Genet. 1993;1(1):88-95. doi: 10.1159/000472391. Eur J Hum Genet. 1993. PMID: 8069655

4

Quantification of tRNA3243(Leu) point mutation of mitochondrial DNA in MELAS patients and its effects on mitochondrial transcription.

Suomalainen A, Majander A, Pihko H, Peltonen L, Syvänen AC. Suomalainen A, et al. Hum Mol Genet. 1993 May;2(5):525-34. doi: 10.1093/hmg/2.5.525. Hum Mol Genet. 1993. PMID: 8518790

5

An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p.

Kaukonen JA, Amati P, Suomalainen A, Rötig A, Piscaglia MG, Salvi F, Weissenbach J, Fratta G, Comi G, Peltonen L, Zeviani M. Kaukonen JA, et al. Among authors: suomalainen a. Am J Hum Genet. 1996 Apr;58(4):763-9. Am J Hum Genet. 1996. PMID: 8644740 Free PMC article.

6

Laminar cortical necrosis in MELAS syndrome: MR and neuropathological observations.

Valanne L, Paetau A, Suomalainen A, Ketonen L, Pihko H. Valanne L, et al. Among authors: suomalainen a. Neuropediatrics. 1996 Jun;27(3):154-60. doi: 10.1055/s-2007-973767. Neuropediatrics. 1996. PMID: 8837076

7

A case of mitochondrial myopathy with MELAS-like features and polyneuropathy: ultrastructural and molecular studies.

Klimek A, Suomalainen A, Bratosiewicz J, Niewinowska-Rupf K, Bogucki A, Liberski PP. Klimek A, et al. Among authors: suomalainen a. Pol J Pathol. 1997;48(3):197-200. Pol J Pathol. 1997. PMID: 9401413 No abstract available.

8

Neuroradiologic findings in children with mitochondrial disorders.

Valanne L, Ketonen L, Majander A, Suomalainen A, Pihko H. Valanne L, et al. Among authors: suomalainen a. AJNR Am J Neuroradiol. 1998 Feb;19(2):369-77. AJNR Am J Neuroradiol. 1998. PMID: 9504497 Free PMC article.

9

A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia.

Kaukonen J, Zeviani M, Comi GP, Piscaglia MG, Peltonen L, Suomalainen A. Kaukonen J, et al. Among authors: suomalainen a. Am J Hum Genet. 1999 Jul;65(1):256-61. doi: 10.1086/302445. Am J Hum Genet. 1999. PMID: 10364542 Free PMC article. No abstract available.

10

Diseases caused by nuclear genes affecting mtDNA stability.

Suomalainen A, Kaukonen J. Suomalainen A, et al. Am J Med Genet. 2001 Spring;106(1):53-61. doi: 10.1002/ajmg.1379. Am J Med Genet. 2001. PMID: 11579425 Review.

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