(21 articles were found) |
| Marti R, et al. Definitive Diagnosis of Mitochondrial Neurogastrointestinal Encephalomyopathy by Biochemical Assays. | |
| Clin Chem 2003 Nov 21;. | |
| Rubinstein JL, et al. Structure of the mitochondrial ATP synthase by electron cryomicroscopy. | |
| EMBO J 2003 Dec 1;22(23):6182-6192. | |
| Ostrow JD, et al. New concepts in bilirubin encephalopathy. | |
| Eur J Clin Invest 2003 Nov;33(11):988-97. | |
| Fonzo AD, et al. POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions. | |
| Hum Mutat 2003 Dec;22(6):498-9. | |
| Kumimoto H, et al. Frequent somatic mutations of mitochondrial DNA in esophageal squamous cell carcinoma. | |
| Int J Cancer 2004 Jan 10;108(2):228-31. | |
| Kowluru RA, et al. Diabetes-induced mitochondrial dysfunction in the retina. | |
| Invest Ophthalmol Vis Sci 2003 Dec;44(12):5327-34. | |
| Monteiro P, et al. Trimetazidine-mediated cardioprotection during ischemia is mediated by mitochondrial respiratory chain's complex I activity. | |
| J Am Coll Cardiol 2003 Mar 19;41(6 Suppl B):373. | |
| Rotig A, et al. Genetic features of mitochondrial respiratory chain disorders. | |
| J Am Soc Nephrol 2003 Dec;14(12):2995-3007. | |
| Truscott KN, et al. A J-protein is an essential subunit of the presequence translocase-associated protein import motor of mitochondria. | |
| J Cell Biol 2003 Nov 24;163(4):707-13. | |
| Puoti G, et al. Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son. | |
| J Med Genet 2003 Nov;40(11):858-63. | |
| Bensasson D, et al. Rates of DNA duplication and mitochondrial DNA insertion in the human genome. | |
| J Mol Evol 2003 Sep;57(3):343-54. | |
| Fernstrom M, et al. Effects of acute and chronic endurance exercise on mitochondrial uncoupling in human skeletal muscle. | |
| J Physiol 2003 Nov 21;. | |
| Arpa J, et al. Prevalence and progression of mitochondrial diseases: A study of 50 patients. | |
| Muscle Nerve 2003 Dec;28(6):690-5.; Review | |
| Ro LS, et al. Deleted 4977-bp mitochondrial DNA mutation is associated with sporadic amyotrophic lateral sclerosis: A hospital-based case-control study. | |
| Muscle Nerve 2003 Dec;28(6):737-43. | |
| Howse ML, et al. Late-onset mitochondrial disorder with electromyographic evidence of myotonia. | |
| Muscle Nerve 2003 Dec;28(6):757-9. | |
| Wood JD, et al. Protein aggregation in motor neurone disorders. | |
| Neuropathol Appl Neurobiol 2003 Dec;29(6):529-45. | |
| Emura I, et al. Morphological investigation of two sibling autopsy cases of mitochondrial trifunctional protein deficiency. | |
| Pathol Int 2003 Nov;53(11):775-9. | |
| Boles RG, et al. Severe reversible cardiomyopathy in four unrelated infants associated with mitochondrial DNA D-loop heteroplasmy. | |
| Pediatr Cardiol 2003 Sep-Oct;24(5):484-7. | |
| Spiekerkoetter U, et al. General Mitochondrial Trifunctional Protein (TFP) Deficiency as a Result of Either {alpha}- or {beta}-Subunit Mutations Exhibits Similar Phenotypes Because Mutations in Either Subunit Alter TFP Complex Expression and Subunit Turnover. | |
| Pediatr Res 2003 Nov 19;. | |
| Vekemans BC, et al. Prenatal diagnosis of carnitine palmitoyltransferase 2 deficiency in chorionic villi: a novel approach. | |
| Prenat Diagn 2003 Nov;23(11):884-7. | |
| Li M, et al. Cadmium directly induced the opening of membrane permeability pore of mitochondria which possibly involved in cadmium-triggered apoptosis. | |
| Toxicology 2003 Dec 15;194(1-2):19-33. | |
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