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2. MERRF: a model disease for understanding the principles of mitochondrial genetics. Shoffner JM; Lott MT; Wallace DC Rev Neurol (Paris); 1991; 147(6-7):431-5. PubMed ID: 1962048 [TBL] [Abstract][Full Text] [Related]
3. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Holt IJ; Harding AE; Morgan-Hughes JA Nature; 1988 Feb; 331(6158):717-9. PubMed ID: 2830540 [TBL] [Abstract][Full Text] [Related]
4. Mitochondrial abnormalities in muscle and other aging cells: classification, causes, and effects. DiMauro S; Tanji K; Bonilla E; Pallotti F; Schon EA Muscle Nerve; 2002 Nov; 26(5):597-607. PubMed ID: 12402281 [TBL] [Abstract][Full Text] [Related]
6. [Clinical aspects of mitochondrial encephalomyopathy--abnormality of mitochondrial respiratory chain]. Nakagawa M; Osame M No To Shinkei; 1990 Aug; 42(8):719-33. PubMed ID: 2121197 [No Abstract] [Full Text] [Related]
7. Mitochondrial myopathies. DiMauro S; Bonilla E; Zeviani M; Nakagawa M; DeVivo DC Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817 [TBL] [Abstract][Full Text] [Related]
8. Mitochondrial disease criteria: diagnostic applications in children. Morava E; van den Heuvel L; Hol F; de Vries MC; Hogeveen M; Rodenburg RJ; Smeitink JA Neurology; 2006 Nov; 67(10):1823-6. PubMed ID: 17130416 [TBL] [Abstract][Full Text] [Related]
9. Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA. Holt IJ; Harding AE; Cooper JM; Schapira AH; Toscano A; Clark JB; Morgan-Hughes JA Ann Neurol; 1989 Dec; 26(6):699-708. PubMed ID: 2604380 [TBL] [Abstract][Full Text] [Related]
10. [Mitochondrial encephalomyopathy]. Scarlato G; Bresolin N; Moggio M; Bet L; Meola G Recenti Prog Med; 1989 Dec; 80(12):665-72. PubMed ID: 2560839 [TBL] [Abstract][Full Text] [Related]
11. [Mitochondrial function and mitochondrial DNA in a series of 64 patients suspected of having mitochondrial myopathy]. Marsac C; Degoul F; Bonne G; Romero N; Nelson I; Fardeau M; François D; Ponsot G; Harpey JP; Eymard B Rev Neurol (Paris); 1991; 147(6-7):462-6. PubMed ID: 1962051 [TBL] [Abstract][Full Text] [Related]
12. Neonatal muscular manifestations in mitochondrial disorders. Tulinius M; Oldfors A Semin Fetal Neonatal Med; 2011 Aug; 16(4):229-35. PubMed ID: 21596636 [TBL] [Abstract][Full Text] [Related]
13. Muscle glycogenosis and mitochondrial hepatopathy in an infant with mutations in both the myophosphorylase and deoxyguanosine kinase genes. Mancuso M; Filosto M; Tsujino S; Lamperti C; Shanske S; Coquet M; Desnuelle C; DiMauro S Arch Neurol; 2003 Oct; 60(10):1445-7. PubMed ID: 14568816 [TBL] [Abstract][Full Text] [Related]
14. Mitochondrial mutations in neuro-ophthalmological diseases. A review. Morris MA J Clin Neuroophthalmol; 1990 Sep; 10(3):159-66. PubMed ID: 2144533 [TBL] [Abstract][Full Text] [Related]
16. [Biochemistry of mitochondrial encephalomyopathy]. Ozawa T; Tanaka M No To Shinkei; 1990 Aug; 42(8):707-17. PubMed ID: 2223265 [No Abstract] [Full Text] [Related]
17. Current perspectives in the study of human mitochondriopathies. Byrne E; Marzuki S; Dennett X Med J Aust; 1988 Jul; 149(1):30-3. PubMed ID: 3290634 [TBL] [Abstract][Full Text] [Related]
18. Epidemiology and treatment of mitochondrial disorders. Chinnery PF; Turnbull DM Am J Med Genet; 2001; 106(1):94-101. PubMed ID: 11579428 [TBL] [Abstract][Full Text] [Related]
19. D-loop mutations in mitochondrial DNA: link with mitochondrial DNA depletion? Barthélémy C; de Baulny HO; Lombès A Hum Genet; 2002 May; 110(5):479-87. PubMed ID: 12073019 [TBL] [Abstract][Full Text] [Related]