Oldfors A - Search Results

1

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.

Horvath R, Kemp JP, Tuppen HA, Hudson G, Oldfors A, Marie SK, Moslemi AR, Servidei S, Holme E, Shanske S, Kollberg G, Jayakar P, Pyle A, Marks HM, Holinski-Feder E, Scavina M, Walter MC, Coku J, Günther-Scholz A, Smith PM, McFarland R, Chrzanowska-Lightowlers ZM, Lightowlers RN, Hirano M, Lochmüller H, Taylor RW, Chinnery PF, Tulinius M, DiMauro S. Horvath R, et al. Among authors: oldfors a. Brain. 2009 Nov;132(Pt 11):3165-74. doi: 10.1093/brain/awp221. Epub 2009 Aug 31. Brain. 2009. PMID: 19720722 Free PMC article.

2

Mitochondrial ATP-synthase deficiency in a child with 3-methylglutaconic aciduria.

Holme E, Greter J, Jacobson CE, Larsson NG, Lindstedt S, Nilsson KO, Oldfors A, Tulinius M. Holme E, et al. Among authors: oldfors a. Pediatr Res. 1992 Dec;32(6):731-5. doi: 10.1203/00006450-199212000-00022. Pediatr Res. 1992. PMID: 1287564

3

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres.

Oldfors A, Larsson NG, Holme E, Tulinius M, Kadenbach B, Droste M. Oldfors A, et al. J Neurol Sci. 1992 Jul;110(1-2):169-77. doi: 10.1016/0022-510x(92)90025-g. J Neurol Sci. 1992. PMID: 1324295

4

Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

Larsson NG, Tulinius MH, Holme E, Oldfors A, Andersen O, Wahlström J, Aasly J. Larsson NG, et al. Among authors: oldfors a. Am J Hum Genet. 1992 Dec;51(6):1201-12. Am J Hum Genet. 1992. PMID: 1463006 Free PMC article.

5

Leber's hereditary optic neuropathy and complex I deficiency in muscle.

Larsson NG, Andersen O, Holme E, Oldfors A, Wahlström J. Larsson NG, et al. Among authors: oldfors a. Ann Neurol. 1991 Nov;30(5):701-8. doi: 10.1002/ana.410300511. Ann Neurol. 1991. PMID: 1763894

6

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations.

Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A. Tulinius MH, et al. Among authors: oldfors a. J Pediatr. 1991 Aug;119(2):242-50. doi: 10.1016/s0022-3476(05)80734-6. J Pediatr. 1991. PMID: 1861209

7

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes.

Tulinius MH, Holme E, Kristiansson B, Larsson NG, Oldfors A. Tulinius MH, et al. Among authors: oldfors a. J Pediatr. 1991 Aug;119(2):251-9. doi: 10.1016/s0022-3476(05)80735-8. J Pediatr. 1991. PMID: 1861210

8

Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome.

Larsson NG, Holme E, Kristiansson B, Oldfors A, Tulinius M. Larsson NG, et al. Among authors: oldfors a. Pediatr Res. 1990 Aug;28(2):131-6. doi: 10.1203/00006450-199008000-00011. Pediatr Res. 1990. PMID: 2395603

9

Cytochrome c oxidase deficiency in infancy.

Oldfors A, Sommerland H, Holme E, Tulinius M, Kristiansson B. Oldfors A, et al. Acta Neuropathol. 1989;77(3):267-75. doi: 10.1007/BF00687578. Acta Neuropathol. 1989. PMID: 2538042

10

Mitochondrial myopathy and cardiomyopathy in siblings.

Tulinius MH, Eriksson BO, Hjalmarson O, Holme E, Oldfors A. Tulinius MH, et al. Among authors: oldfors a. Pediatr Neurol. 1989 May-Jun;5(3):182-8. doi: 10.1016/0887-8994(89)90069-6. Pediatr Neurol. 1989. PMID: 2742628

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

296 results

Search Page