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Journal Abstract Search
227 related items for PubMed ID: 2855955
1. [Abnormality in the mitochondrial energy-producing system]. Ozawa T, Tanaka M. Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):824-7. PubMed ID: 2855955 [No Abstract] [Full Text] [Related]
2. Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study. Bindoff LA, Desnuelle C, Birch-Machin MA, Pellissier JF, Serratrice G, Dravet C, Bureau M, Howell N, Turnbull DM. J Neurol Sci; 1991 Mar; 102(1):17-24. PubMed ID: 1649912 [Abstract] [Full Text] [Related]
8. Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria. Watmough NJ, Bindoff LA, Birch-Machin MA, Jackson S, Bartlett K, Ragan CI, Poulton J, Gardiner RM, Sherratt HS, Turnbull DM. J Clin Invest; 1990 Jan 05; 85(1):177-84. PubMed ID: 2153151 [Abstract] [Full Text] [Related]
9. Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies. Tanaka M, Nishikimi M, Suzuki H, Ozawa T, Koga Y, Nonaka I. Biochem Int; 1987 Mar 05; 14(3):525-30. PubMed ID: 2884999 [Abstract] [Full Text] [Related]
11. Impaired energy metabolism in hearts of septic baboons: diminished activities of Complex I and Complex II of the mitochondrial respiratory chain. Gellerich FN, Trumbeckaite S, Hertel K, Zierz S, Müller-Werdan U, Werdan K, Redl H, Schlag G. Shock; 1999 May 05; 11(5):336-41. PubMed ID: 10353539 [Abstract] [Full Text] [Related]
12. Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathy. Desnuelle C, Birch-Machin M, Pellissier JF, Bindoff LA, Ackrell BA, Turnbull DM. Biochem Biophys Res Commun; 1989 Sep 15; 163(2):695-700. PubMed ID: 2551272 [Abstract] [Full Text] [Related]
13. [Electron transfer complex II deficiency]. Goto Y. Ryoikibetsu Shokogun Shirizu; 1998 Sep 15; (19 Pt 2):491-3. PubMed ID: 9645117 [No Abstract] [Full Text] [Related]
14. [Complex II deficiency due to Fp gene mutation]. Ito M. Nihon Rinsho; 2002 Apr 15; 60 Suppl 4():444-5. PubMed ID: 12013908 [No Abstract] [Full Text] [Related]
16. Human mitochondrial respiratory chain deficiencies. Morgan-Hughes JA, Schapira AH, Cooper JM, Hayes DJ, Clark JB. Aust Paediatr J; 1988 Apr 15; 24 Suppl 1():55-7. PubMed ID: 2849394 [Abstract] [Full Text] [Related]
17. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features. Thyagarajan D, Byrne E. Int Rev Neurobiol; 2002 Apr 15; 53():93-144. PubMed ID: 12512338 [No Abstract] [Full Text] [Related]
18. Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease. Hattori N, Tanaka M, Ozawa T, Mizuno Y. Ann Neurol; 1991 Oct 15; 30(4):563-71. PubMed ID: 1665052 [Abstract] [Full Text] [Related]
19. Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV. Rubio-Gozalbo ME, Ruitenbeek W, Bentlage HA, Schägger H, Sengers RC, Trijbels JM, ter Laak HJ, Mariman EC, Bakker MM, de Jager J, Smeitink JA. Eur J Pediatr; 1997 Dec 15; 156(12):931-4. PubMed ID: 9453375 [Abstract] [Full Text] [Related]
20. The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system. Morgan-Hughes JA, Cooper JM, Schapira AH, Hayes DJ, Clark JB. Electroencephalogr Clin Neurophysiol Suppl; 1987 Dec 15; 39():103-14. PubMed ID: 2888641 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]