Haltia M - Search Results

1

Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.

Suomalainen A, Majander A, Haltia M, Somer H, Lönnqvist J, Savontaus ML, Peltonen L. Suomalainen A, et al. Among authors: haltia m. J Clin Invest. 1992 Jul;90(1):61-6. doi: 10.1172/JCI115856. J Clin Invest. 1992. PMID: 1634620 Free PMC article.

2

An autosomal locus predisposing to deletions of mitochondrial DNA.

Suomalainen A, Kaukonen J, Amati P, Timonen R, Haltia M, Weissenbach J, Zeviani M, Somer H, Peltonen L. Suomalainen A, et al. Among authors: haltia m. Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146. Nat Genet. 1995. PMID: 7719341

3

Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.

Suomalainen A, Majander A, Wallin M, Setälä K, Kontula K, Leinonen H, Salmi T, Paetau A, Haltia M, Valanne L, Lonnqvist J, Peltonen L, Somer H. Suomalainen A, et al. Among authors: haltia m. Neurology. 1997 May;48(5):1244-53. doi: 10.1212/wnl.48.5.1244. Neurology. 1997. PMID: 9153451

4

Disorders associated with multiple deletions of mitochondrial DNA.

Haltia M, Suomalainen A, Majander A, Somer H. Haltia M, et al. Brain Pathol. 1992 Apr;2(2):133-9. doi: 10.1111/j.1750-3639.1992.tb00681.x. Brain Pathol. 1992. PMID: 1341954 Review.

5

[Mitochondrial diseases].

Pihko H, Suomalainen A, Somer H, Haltia M, Majander A. Pihko H, et al. Among authors: haltia m. Duodecim. 1992;108(6):578-90. Duodecim. 1992. PMID: 1366118 Review. Finnish. No abstract available.

6

Linkage map of the chromosomal region surrounding the infantile neuronal ceroid lipofuscinosis on 1p.

Järvelä I, Santavuori P, Puhakka L, Haltia M, Peltonen L. Järvelä I, et al. Among authors: haltia m. Am J Med Genet. 1992 Feb 15;42(4):546-8. doi: 10.1002/ajmg.1320420425. Am J Med Genet. 1992. PMID: 1609836

7

Adult onset limb-girdle muscular dystrophy with autosomal dominant inheritance.

Somer H, Laulumaa V, Paljärvi L, Partanen J, Haltia M. Somer H, et al. Among authors: haltia m. Prog Clin Biol Res. 1989;306:69-71. Prog Clin Biol Res. 1989. PMID: 2740412 No abstract available.

8

Congenital fiber type disproportion in an adult: a morphometric and microchemical study.

Haltia M, Somer H, Rehunen S. Haltia M, et al. Acta Neurol Scand. 1988 Jul;78(1):65-71. doi: 10.1111/j.1600-0404.1988.tb03621.x. Acta Neurol Scand. 1988. PMID: 2972157

9

Neuromuscular pathology in hereditary gelsolin amyloidosis.

Kiuru-Enari S, Somer H, Seppäläinen AM, Notkola IL, Haltia M. Kiuru-Enari S, et al. Among authors: haltia m. J Neuropathol Exp Neurol. 2002 Jun;61(6):565-71. doi: 10.1093/jnen/61.6.565. J Neuropathol Exp Neurol. 2002. PMID: 12071640

10

Toward understanding the pathogenic mechanisms in gelsolin-related amyloidosis: in vitro expression reveals an abnormal gelsolin fragment.

Paunio T, Kangas H, Kalkkinen N, Haltia M, Palo J, Peltonen L. Paunio T, et al. Among authors: haltia m. Hum Mol Genet. 1994 Dec;3(12):2223-9. doi: 10.1093/hmg/3.12.2223. Hum Mol Genet. 1994. PMID: 7881424

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