Oldfors A - Search Results

1

Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial disease.

Westerlund E, Marelsson SE, Ehinger JK, Sjövall F, Morota S, Åsander Frostner E, Oldfors A, Darin N, Lundgren J, Hansson MJ, Fellman V, Elmér E. Westerlund E, et al. Among authors: oldfors a. Pediatr Res. 2018 Feb;83(2):455-465. doi: 10.1038/pr.2017.250. Epub 2017 Nov 15. Pediatr Res. 2018. PMID: 28981487

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

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

4

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

5

Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles.

Darin N, Kyllerman M, Wahlström J, Martinsson T, Oldfors A. Darin N, et al. Among authors: oldfors a. Ann Neurol. 1998 Aug;44(2):242-8. doi: 10.1002/ana.410440215. Ann Neurol. 1998. PMID: 9708547

6

Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.

Jansson M, Darin N, Kyllerman M, Martinsson T, Wahlström J, Oldfors A. Jansson M, et al. Among authors: oldfors a. Acta Neuropathol. 2000 Jul;100(1):23-8. doi: 10.1007/s004010051188. Acta Neuropathol. 2000. PMID: 10912916

7

The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities.

Darin N, Oldfors A, Moslemi AR, Holme E, Tulinius M. Darin N, et al. Among authors: oldfors a. Ann Neurol. 2001 Mar;49(3):377-83. Ann Neurol. 2001. PMID: 11261513

8

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age.

Tajsharghi H, Thornell LE, Darin N, Martinsson T, Kyllerman M, Wahlström J, Oldfors A. Tajsharghi H, et al. Among authors: oldfors a. Neurology. 2002 Mar 12;58(5):780-6. doi: 10.1212/wnl.58.5.780. Neurology. 2002. PMID: 11889243

9

Leigh syndrome with cytochrome-c oxidase deficiency and a single T insertion nt 5537 in the mitochondrial tRNATrp gene.

Tulinius M, Moslemi AR, Darin N, Westerberg B, Wiklund LM, Holme E, Oldfors A. Tulinius M, et al. Among authors: oldfors a. Neuropediatrics. 2003 Apr;34(2):87-91. doi: 10.1055/s-2003-39607. Neuropediatrics. 2003. PMID: 12776230

10

Induced shift in myosin heavy chain expression in myosin myopathy by endurance training.

Tajsharghi H, Sunnerhagen KS, Darin N, Kyllerman M, Oldfors A. Tajsharghi H, et al. Among authors: oldfors a. J Neurol. 2004 Feb;251(2):179-83. doi: 10.1007/s00415-004-0295-5. J Neurol. 2004. PMID: 14991352

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

303 results

Search Page

Filters