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

2

Disorders associated with multiple deletions of mitochondrial DNA.

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

3

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. Lancet. 1992 Nov 28;340(8831):1319-20. doi: 10.1016/0140-6736(92)92496-3. Lancet. 1992. PMID: 1360038

4

[Mitochondrial diseases].

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

5

[Short stature and calcium deposits in the brain of an 8-year-old girl].

Pihko H, Suomalainen A, Majander A, Wallden T. Pihko H, et al. Among authors: suomalainen a. Duodecim. 1992;108(6):603-6. Duodecim. 1992. PMID: 1366121 Finnish. No abstract available.

6

Use of single strand conformation polymorphism analysis to detect point mutations in human mitochondrial DNA.

Suomalainen A, Ciafaloni E, Koga Y, Peltonen L, DiMauro S, Schon EA. Suomalainen A, et al. J Neurol Sci. 1992 Sep;111(2):222-6. doi: 10.1016/0022-510x(92)90074-u. J Neurol Sci. 1992. PMID: 1431990

7

PCR in the analysis of mutations in mitochondrial DNA.

Suomalainen A. Suomalainen A. Ann Med. 1992 Jun;24(3):201-5. doi: 10.3109/07853899209147822. Ann Med. 1992. PMID: 1627317 Free article. Review. No abstract available.

8

Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion.

Majander A, Suomalainen A, Vettenranta K, Sariola H, Perkkiö M, Holmberg C, Pihko H. Majander A, et al. Among authors: suomalainen a. Pediatr Res. 1991 Oct;30(4):327-30. doi: 10.1203/00006450-199110000-00007. Pediatr Res. 1991. PMID: 1956715

9

Correlation between the clinical symptoms and the proportion of mitochondrial DNA carrying the 8993 point mutation in the NARP syndrome.

Mäkelä-Bengs P, Suomalainen A, Majander A, Rapola J, Kalimo H, Nuutila A, Pihko H. Mäkelä-Bengs P, et al. Among authors: suomalainen a. Pediatr Res. 1995 May;37(5):634-9. doi: 10.1203/00006450-199505000-00014. Pediatr Res. 1995. PMID: 7603783

10

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

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

257 results

Search Page

Filters