Somer H - 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: somer h. J Clin Invest. 1992 Jul;90(1):61-6. doi: 10.1172/JCI115856. J Clin Invest. 1992. PMID: 1634620 Free PMC article.

2

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: somer h. Neurology. 1997 May;48(5):1244-53. doi: 10.1212/wnl.48.5.1244. Neurology. 1997. PMID: 9153451

3

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: somer h. Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146. Nat Genet. 1995. PMID: 7719341

4

Disorders associated with multiple deletions of mitochondrial DNA.

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

5

Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNA.

Suomalainen A, Paetau A, Leinonen H, Majander A, Peltonen L, Somer H. Suomalainen A, et al. Among authors: somer h. Lancet. 1992 Nov 28;340(8831):1319-20. doi: 10.1016/0140-6736(92)92496-3. Lancet. 1992. PMID: 1360038

6

Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.

Luoma P, Melberg A, Rinne JO, Kaukonen JA, Nupponen NN, Chalmers RM, Oldfors A, Rautakorpi I, Peltonen L, Majamaa K, Somer H, Suomalainen A. Luoma P, et al. Among authors: somer h. Lancet. 2004 Sep 4-10;364(9437):875-82. doi: 10.1016/S0140-6736(04)16983-3. Lancet. 2004. PMID: 15351195

7

ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's disease.

Löfberg M, Lindholm H, Näveri H, Majander A, Suomalainen A, Paetau A, Sovijärvi A, Härkönen M, Somer H. Löfberg M, et al. Among authors: somer h. Neuromuscul Disord. 2001 May;11(4):370-5. doi: 10.1016/s0960-8966(00)00205-4. Neuromuscul Disord. 2001. PMID: 11369188

8

[Mitochondrial diseases].

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

9

Gene deletions in X-linked muscular dystrophy.

Lindlöf M, Kiuru A, Kääriäinen H, Kalimo H, Lang H, Pihko H, Rapola J, Somer H, Somer M, Savontaus ML, et al. Lindlöf M, et al. Among authors: somer h, somer m. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.

10

Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish population.

Nokelainen P, Alanen-Kurki L, Winqvist R, Falck B, Somer H, Leisti J, Johnson K, Savontaus ML, Peltonen L. Nokelainen P, et al. Among authors: somer h. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

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