Savontaus ML - 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: savontaus ml. J Clin Invest. 1992 Jul;90(1):61-6. doi: 10.1172/JCI115856. J Clin Invest. 1992. PMID: 1634620 Free PMC article.

2

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: savontaus ml. Am J Hum Genet. 1989 Apr;44(4):496-503. Am J Hum Genet. 1989. PMID: 2929594 Free PMC article.

3

Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON).

Majander A, Huoponen K, Savontaus ML, Nikoskelainen E, Wikström M. Majander A, et al. Among authors: savontaus ml. FEBS Lett. 1991 Nov 4;292(1-2):289-92. doi: 10.1016/0014-5793(91)80886-8. FEBS Lett. 1991. PMID: 1959619 Free article.

4

Mutations in subunit 6 of the F1F0-ATP synthase cause two entirely different diseases.

Majander A, Lamminen T, Juvonen V, Aula P, Nikoskelainen E, Savontaus ML, Wikström M. Majander A, et al. Among authors: savontaus ml. FEBS Lett. 1997 Jul 28;412(2):351-4. doi: 10.1016/s0014-5793(97)00757-6. FEBS Lett. 1997. PMID: 9256250 Free article.

5

The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNA.

Lahermo P, Sajantila A, Sistonen P, Lukka M, Aula P, Peltonen L, Savontaus ML. Lahermo P, et al. Among authors: savontaus ml. Am J Hum Genet. 1996 Jun;58(6):1309-22. Am J Hum Genet. 1996. PMID: 8651309 Free PMC article.

6

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: savontaus ml. Hum Genet. 1990 Oct;85(5):541-5. doi: 10.1007/BF00194234. Hum Genet. 1990. PMID: 1977684

7

Gene defects in Leber hereditary optic neuroretinopathy.

Savontaus ML, Huoponen K, Majander A, Aula P, Nikoskelainen EK. Savontaus ML, et al. Biochim Biophys Acta. 1992 Jul 17;1101(2):204-5. Biochim Biophys Acta. 1992. PMID: 1633186 Review. No abstract available.

8

Catalytic activity of complex I in cell lines that possess replacement mutations in the ND genes in Leber's hereditary optic neuropathy.

Majander A, Finel M, Savontaus ML, Nikoskelainen E, Wikström M. Majander A, et al. Among authors: savontaus ml. Eur J Biochem. 1996 Jul 1;239(1):201-7. doi: 10.1111/j.1432-1033.1996.0201u.x. Eur J Biochem. 1996. PMID: 8706709 Free article.

9

The DM mutation; diagnostic applications in the Finnish population.

Nokelainen P, Shelbourne P, Shaw D, Brook JD, Harley HG, Johnson K, Somer H, Savontaus ML, Peltonen L. Nokelainen P, et al. Among authors: savontaus ml. Clin Genet. 1993 Apr;43(4):190-5. doi: 10.1111/j.1399-0004.1993.tb04446.x. Clin Genet. 1993. PMID: 8101149

10

Benzodiazepine sensitivity in Leber's hereditary optic neuroretinopathy.

Nikoskelainen E, Asola M, Kalimo H, Savontaus ML, Majander A. Nikoskelainen E, et al. Among authors: savontaus ml. Lancet. 1992 Nov 14;340(8829):1223-4. doi: 10.1016/0140-6736(92)92925-6. Lancet. 1992. PMID: 1359290 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

109 results

Search Page

Filters