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Journal Abstract Search
232 related items for PubMed ID: 9678512
1. 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 [Abstract] [Full Text] [Related]
2. Polymyositis with mitochondrial pathology or atypical form of sporadic inclusion body myositis: case series and review of the literature. Papadimas GK, Kokkinis C, Xirou S, Chrysanthou M, Kararizou E, Papadopoulos C. Rheumatol Int; 2019 Aug; 39(8):1459-1466. PubMed ID: 31055642 [Abstract] [Full Text] [Related]
3. 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 [Abstract] [Full Text] [Related]
6. Ubiquitin immunostaining and inclusion body myositis: study of 30 patients with inclusion body myositis. Prayson RA, Cohen ML. Hum Pathol; 1997 Aug; 28(8):887-92. PubMed ID: 9269823 [Abstract] [Full Text] [Related]
7. Characterization of the mitochondrial DNA abnormalities in the skeletal muscle of patients with inclusion body myositis. Horvath R, Fu K, Johns T, Genge A, Karpati G, Shoubridge EA. J Neuropathol Exp Neurol; 1998 May; 57(5):396-403. PubMed ID: 9596410 [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 [Abstract] [Full Text] [Related]
9. Congenital myopathy with tubular aggregates and tubulofilamentous IBM-type inclusions. Fidziańska A, Kamińska A, Ryniewicz B. Neuropediatrics; 2005 Feb; 36(1):35-9. PubMed ID: 15776320 [Abstract] [Full Text] [Related]
10. Inflammatory myopathies with mitochondrial pathology and protein aggregates. Temiz P, Weihl CC, Pestronk A. J Neurol Sci; 2009 Mar 15; 278(1-2):25-9. PubMed ID: 19101700 [Abstract] [Full Text] [Related]
11. Mitochondrial abnormalities and peripheral neuropathy in inflammatory myopathy, especially inclusion body myositis. Schröder JM, Molnar M. Mol Cell Biochem; 1997 Sep 15; 174(1-2):277-81. PubMed ID: 9309700 [Abstract] [Full Text] [Related]
12. Bcl-2, Bcl-x, and Bax expression by immunohistochemistry in inclusion body myositis: a study of 27 cases. Prayson RA, Yu AC. Arch Pathol Lab Med; 2001 Oct 15; 125(10):1326-30. PubMed ID: 11570908 [Abstract] [Full Text] [Related]
13. Quantitative morphometric study of muscle in inclusion body myositis. Verma A, Bradley WG, Soule NW, Pendlebury WW, Kelly J, Adelman LS, Chou SM, Karpati G, Brenner JF. J Neurol Sci; 1992 Oct 15; 112(1-2):192-8. PubMed ID: 1335036 [Abstract] [Full Text] [Related]
14. 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 15; 21(11):1959-63. PubMed ID: 25311418 [Abstract] [Full Text] [Related]
15. Mitochondrial pathology in inclusion body myositis. Lindgren U, Roos S, Hedberg Oldfors C, Moslemi AR, Lindberg C, Oldfors A. Neuromuscul Disord; 2015 Apr 15; 25(4):281-8. PubMed ID: 25638290 [Abstract] [Full Text] [Related]
16. T-Cell-Mediated Inflammatory Myopathies in HIV-Positive Individuals: A Histologic Study of 19 Cases. Hiniker A, Daniels BH, Margeta M. J Neuropathol Exp Neurol; 2016 Mar 15; 75(3):239-45. PubMed ID: 26843609 [Abstract] [Full Text] [Related]
17. [Inclusion body myositis and neuromuscular diseases with rimmed vacuoles]. Figarella-Branger D, Pellissier JF, Pouget J, Calore EE, Azulay JP, Desnuelle C, Serratrice G. Rev Neurol (Paris); 1992 Mar 15; 148(4):281-90. PubMed ID: 1332175 [Abstract] [Full Text] [Related]
18. Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments. Mendell JR, Sahenk Z, Gales T, Paul L. Arch Neurol; 1991 Dec 15; 48(12):1229-34. PubMed ID: 1668977 [Abstract] [Full Text] [Related]
19. p62/SQSTM1 is overexpressed and prominently accumulated in inclusions of sporadic inclusion-body myositis muscle fibers, and can help differentiating it from polymyositis and dermatomyositis. Nogalska A, Terracciano C, D'Agostino C, King Engel W, Askanas V. Acta Neuropathol; 2009 Sep 15; 118(3):407-13. PubMed ID: 19557423 [Abstract] [Full Text] [Related]