451 related articles for article (PubMed ID: 16432145)
1. Mitochondrial abnormalities in inclusion-body myositis.
Oldfors A; Moslemi AR; Jonasson L; Ohlsson M; Kollberg G; Lindberg C
Neurology; 2006 Jan; 66(2 Suppl 1):S49-55. PubMed ID: 16432145
[TBL] [Abstract][Full Text] [Related]
2. Analysis of multiple mitochondrial DNA deletions in inclusion body myositis.
Moslemi AR; Lindberg C; Oldfors A
Hum Mutat; 1997; 10(5):381-6. PubMed ID: 9375854
[TBL] [Abstract][Full Text] [Related]
3. Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.
Santorelli FM; Sciacco M; Tanji K; Shanske S; Vu TH; Golzi V; Griggs RC; Mendell JR; Hays AP; Bertorini TE; Pestronk A; Bonilla E; DiMauro S
Ann Neurol; 1996 Jun; 39(6):789-95. PubMed ID: 8651651
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial DNA deletions in muscle fibers in inclusion body myositis.
Oldfors A; Moslemi AR; Fyhr IM; Holme E; Larsson NG; Lindberg C
J Neuropathol Exp Neurol; 1995 Jul; 54(4):581-7. PubMed ID: 7602331
[TBL] [Abstract][Full Text] [Related]
5. Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.
Auré K; Fayet G; Leroy JP; Lacène E; Romero NB; Lombès A
Brain; 2006 May; 129(Pt 5):1249-59. PubMed ID: 16537564
[TBL] [Abstract][Full Text] [Related]
6. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia.
Moslemi AR; Melberg A; Holme E; Oldfors A
Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011
[TBL] [Abstract][Full Text] [Related]
7. Association of myopathy with large-scale mitochondrial DNA duplications and deletions: which is pathogenic?
Manfredi G; Vu T; Bonilla E; Schon EA; DiMauro S; Arnaudo E; Zhang L; Rowland LP; Hirano M
Ann Neurol; 1997 Aug; 42(2):180-8. PubMed ID: 9266727
[TBL] [Abstract][Full Text] [Related]
8. Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing.
Hedberg-Oldfors C; Lindgren U; Basu S; Visuttijai K; Lindberg C; Falkenberg M; Larsson Lekholm E; Oldfors A
Brain Pathol; 2021 May; 31(3):e12931. PubMed ID: 33354847
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial pathology in inclusion body myositis.
Lindgren U; Roos S; Hedberg Oldfors C; Moslemi AR; Lindberg C; Oldfors A
Neuromuscul Disord; 2015 Apr; 25(4):281-8. PubMed ID: 25638290
[TBL] [Abstract][Full Text] [Related]
10. Low frequency of mtDNA point mutations in patients with PEO associated with POLG1 mutations.
Kollberg G; Jansson M; Pérez-Bercoff A; Melberg A; Lindberg C; Holme E; Moslemi AR; Oldfors A
Eur J Hum Genet; 2005 Apr; 13(4):463-9. PubMed ID: 15702133
[TBL] [Abstract][Full Text] [Related]
11. Functional relevance of mitochondrial abnormalities in sporadic inclusion body myositis.
Joshi PR; Vetterke M; Hauburger A; Tacik P; Stoltenburg G; Hanisch F
J Clin Neurosci; 2014 Nov; 21(11):1959-63. PubMed ID: 25311418
[TBL] [Abstract][Full Text] [Related]
12. Age-dependent respiratory function decline and DNA deletions in human muscle mitochondria.
Hsieh RH; Hou JH; Hsu HS; Wei YH
Biochem Mol Biol Int; 1994 Apr; 32(6):1009-22. PubMed ID: 8061617
[TBL] [Abstract][Full Text] [Related]
13. Multiple mitochondrial DNA deletions in hereditary inclusion body myopathy.
Jansson M; Darin N; Kyllerman M; Martinsson T; Wahlström J; Oldfors A
Acta Neuropathol; 2000 Jul; 100(1):23-8. PubMed ID: 10912916
[TBL] [Abstract][Full Text] [Related]
14. Mitochondrial (mt)DNA changes in tissue may not be reflected by depletion of mtDNA in peripheral blood mononuclear cells in HIV-infected patients.
Maagaard A; Holberg-Petersen M; Kollberg G; Oldfors A; Sandvik L; Bruun JN
Antivir Ther; 2006; 11(5):601-8. PubMed ID: 16964828
[TBL] [Abstract][Full Text] [Related]
15. POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
Di Fonzo A; Bordoni A; Crimi M; Sara G; Del Bo R; Bresolin N; Comi GP
Hum Mutat; 2003 Dec; 22(6):498-9. PubMed ID: 14635118
[TBL] [Abstract][Full Text] [Related]
16. Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions.
Molnar M; Schröder JM
Acta Neuropathol; 1998 Jul; 96(1):41-51. PubMed ID: 9678512
[TBL] [Abstract][Full Text] [Related]
17. Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes.
Rostedt Punga A; Ahlqvist K; Bartoccioni E; Scuderi F; Marino M; Suomalainen A; Kalimo H; Stålberg EV
Clin Neurophysiol; 2006 Jul; 117(7):1434-43. PubMed ID: 16737845
[TBL] [Abstract][Full Text] [Related]
18. Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies.
Filosto M; Mancuso M; Vives-Bauza C; Vilà MR; Shanske S; Hirano M; Andreu AL; DiMauro S
Ann Neurol; 2003 Oct; 54(4):524-6. PubMed ID: 14520667
[TBL] [Abstract][Full Text] [Related]
19. Spectrum of myopathic findings in 50 patients with the 3243A>G mutation in mitochondrial DNA.
Kärppä M; Herva R; Moslemi AR; Oldfors A; Kakko S; Majamaa K
Brain; 2005 Aug; 128(Pt 8):1861-9. PubMed ID: 15857931
[TBL] [Abstract][Full Text] [Related]
20. Correlation of functional and ultrastructural abnormalities of mitochondria in mouse heart carrying a pathogenic mutant mtDNA with a 4696-bp deletion.
Nakada K; Inoue K; Chen CS; Nonaka I; Goto Y; Ogura A; Hayashi JI
Biochem Biophys Res Commun; 2001 Nov; 288(4):901-7. PubMed ID: 11688994
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]