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9. Mitochondrial DNA and RNA processing in MELAS. Kaufmann P; Koga Y; Shanske S; Hirano M; DiMauro S; King MP; Schon EA Ann Neurol; 1996 Aug; 40(2):172-80. PubMed ID: 8773598 [TBL] [Abstract][Full Text] [Related]
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11. Pathology of mitochondria in MELAS syndrome: an ultrastructural study. Felczak P; Lewandowska E; Stępniak I; Ołdak M; Pollak A; Lechowicz U; Pasennik E; Stępień T; Wierzba-Bobrowicz T Pol J Pathol; 2017; 68(2):173-181. PubMed ID: 29025253 [TBL] [Abstract][Full Text] [Related]
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13. Diagnosis and management of MELAS. Thambisetty M; Newman NJ Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257 [TBL] [Abstract][Full Text] [Related]
14. Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation. Bataillard M; Chatzoglou E; Rumbach L; Sternberg D; Tournade A; Laforêt P; Jardel C; Maisonobe T; Lombès A Neurology; 2001 Feb; 56(3):405-7. PubMed ID: 11171912 [TBL] [Abstract][Full Text] [Related]
15. Clinical and genetic features in a MELAS child with a 3271T>C mutation. Chou HF; Liang WC; Zhang Q; Goto Y; Jong YJ Pediatr Neurol; 2008 Feb; 38(2):143-6. PubMed ID: 18206799 [TBL] [Abstract][Full Text] [Related]
16. The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families. Vilarinho L; Santorelli FM; Coelho I; Rodrigues L; Maia M; Barata I; Cabral P; Dionísio A; Costa A; Guimarães A; DiMauro S J Neurol Sci; 1999 Mar; 163(2):168-74. PubMed ID: 10371079 [TBL] [Abstract][Full Text] [Related]
17. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA. Terauchi A; Tamagawa K; Morimatsu Y; Kobayashi M; Sano T; Yoda S Brain Dev; 1996; 18(3):224-9. PubMed ID: 8836506 [TBL] [Abstract][Full Text] [Related]
18. MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation. Connolly BS; Feigenbaum AS; Robinson BH; Dipchand AI; Simon DK; Tarnopolsky MA Biochem Biophys Res Commun; 2010 Nov; 402(2):443-7. PubMed ID: 20965148 [TBL] [Abstract][Full Text] [Related]
19. Clinical, physiological, and histological features in a kindred with the T3271C melas mutation. Tarnopolsky MA; Maguire J; Myint T; Applegarth D; Robinson BH Muscle Nerve; 1998 Jan; 21(1):25-33. PubMed ID: 9427220 [TBL] [Abstract][Full Text] [Related]
20. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS). Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]