These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. Mitochondrial dysfunction in skeletal muscle of children with cardiomyopathy. Marin-Garcia J; Ananthakrishnan R; Goldenthal MJ; Filiano JJ; Perez-Atayde A Pediatrics; 1999 Feb; 103(2):456-9. PubMed ID: 9925841 [TBL] [Abstract][Full Text] [Related]
6. Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients harboring the A3243G point mutation or large-scale deletions of mitochondrial DNA. Vielhaber S; Varlamov DA; Kudina TA; Schröder R; Kappes-Horn K; Elger CE; Seibel M; Seibel P; Kunz WS J Neuropathol Exp Neurol; 2002 Oct; 61(10):885-95. PubMed ID: 12387454 [TBL] [Abstract][Full Text] [Related]
7. Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders. Uusimaa J; Remes AM; Rantala H; Vainionpää L; Herva R; Vuopala K; Nuutinen M; Majamaa K; Hassinen IE Pediatrics; 2000 Mar; 105(3 Pt 1):598-603. PubMed ID: 10699115 [TBL] [Abstract][Full Text] [Related]
8. Unaltered respiratory chain enzyme activity and mitochondrial DNA in skeletal muscle from patients with idiopathic Parkinson's syndrome. Reichmann H; Janetzky B; Bischof F; Seibel P; Schöls L; Kuhn W; Przuntek H Eur Neurol; 1994; 34(5):263-7. PubMed ID: 7995300 [TBL] [Abstract][Full Text] [Related]
9. Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system. Janssen AJ; Schuelke M; Smeitink JA; Trijbels FJ; Sengers RC; Lucke B; Wintjes LT; Morava E; van Engelen BG; Smits BW; Hol FA; Siers MH; Ter Laak H; van der Knaap MS; Van Spronsen FJ; Rodenburg RJ; van den Heuvel LP Ann Neurol; 2008 Apr; 63(4):473-81. PubMed ID: 18306232 [TBL] [Abstract][Full Text] [Related]
10. Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype. Ignatieva E; Smolina N; Kostareva A; Dmitrieva R Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34298968 [TBL] [Abstract][Full Text] [Related]
11. Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies. Jaksch M; Kleinle S; Scharfe C; Klopstock T; Pongratz D; Müller-Höcker J; Gerbitz KD; Liechti-Gallati S; Lochmuller H; Horvath R J Med Genet; 2001 Oct; 38(10):665-73. PubMed ID: 11584044 [TBL] [Abstract][Full Text] [Related]
12. Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes. Tulinius MH; Holme E; Kristiansson B; Larsson NG; Oldfors A J Pediatr; 1991 Aug; 119(2):251-9. PubMed ID: 1861210 [TBL] [Abstract][Full Text] [Related]
13. Non-invasive evaluation of buccal respiratory chain enzyme dysfunction in mitochondrial disease: comparison with studies in muscle biopsy. Goldenthal MJ; Kuruvilla T; Damle S; Salganicoff L; Sheth S; Shah N; Marks H; Khurana D; Valencia I; Legido A Mol Genet Metab; 2012 Mar; 105(3):457-62. PubMed ID: 22189081 [TBL] [Abstract][Full Text] [Related]
14. New insights into the metabolic consequences of large-scale mtDNA deletions: a quantitative analysis of biochemical, morphological, and genetic findings in human skeletal muscle. Schröder R; Vielhaber S; Wiedemann FR; Kornblum C; Papassotiropoulos A; Broich P; Zierz S; Elger CE; Reichmann H; Seibel P; Klockgether T; Kunz WS J Neuropathol Exp Neurol; 2000 May; 59(5):353-60. PubMed ID: 10888364 [TBL] [Abstract][Full Text] [Related]
15. Mitochondrial myopathies-clinicopathological features and diagnostic modalities. Tatke M Indian J Pathol Microbiol; 2007 Jul; 50(3):467-77. PubMed ID: 17883111 [TBL] [Abstract][Full Text] [Related]
16. Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders. Mkaouar-Rebai E; Felhi R; Tabebi M; Alila-Fersi O; Chamkha I; Maalej M; Ammar M; Kammoun F; Keskes L; Hachicha M; Fakhfakh F Biochem Biophys Res Commun; 2016 Apr; 473(2):578-85. PubMed ID: 27033601 [TBL] [Abstract][Full Text] [Related]
17. Polarographic evaluation of mitochondrial enzymes activity in isolated mitochondria and in permeabilized human muscle cells with inherited mitochondrial defects. Wenchich L; Drahota Z; Honzík T; Hansíková H; Tesarová M; Zeman J; Houstek J Physiol Res; 2003; 52(6):781-8. PubMed ID: 14640901 [TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA depletion in Leigh syndrome. Filiano JJ; Goldenthal MJ; Mamourian AC; Hall CC; Marín-García J Pediatr Neurol; 2002 Mar; 26(3):239-42. PubMed ID: 11955936 [TBL] [Abstract][Full Text] [Related]