| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/BF00314404 |
| P698 | PubMed publication ID | 2709060 |
| P2093 | author name string | S Zierz | |
| G Jahns | |||
| F Jerusalem | |||
| P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
| Improvement of abnormal pyruvate metabolism and cardiac conduction defect with coenzyme Q10 in Kearns-Sayre syndrome | Q28307882 | ||
| Biochemical rationale and the cardiac response of patients with muscle disease to therapy with coenzyme Q10. | Q37546171 | ||
| Diabetes mellitus in Kearns-Sayre syndrome | Q39640018 | ||
| Atypical form of Menkes kinky hair disease with mitochondrial NADH-CoQ reductase deficiency | Q44213647 | ||
| Mitochondrial Encephalomyopathy with Sleep Apnea | Q48130156 | ||
| Chronic progressive external ophthalmoplegia (CPEO): Clinical, morphologic, and biochemical studies | Q67280198 | ||
| Letter: Progressive external ophthalmoplegia: evidence for a disorder in pyruvate-lactate metabolism | Q67754028 | ||
| Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10 | Q68352956 | ||
| Aggregation and diffusion in the mitochondrial electron-transfer chain: role in electron flow and energy transfer | Q69662073 | ||
| Clinical improvement after administration of coenzyme Q10 in a patient with mitochondrial encephalomyopathy | Q69755914 | ||
| A relay model of lipid peroxidation in biological membranes | Q69797469 | ||
| Mitochondrial myopathies | Q69958309 | ||
| Treatment of Kearns-Sayre syndrome with coenzyme Q10 | Q69991702 | ||
| Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study | Q70182429 | ||
| Fluidizing effect of endogenous ubiquinone in bovine heart mitochondrial membranes | Q70218326 | ||
| Lateral diffusion of ubiquinone during electron transfer in phospholipid- and ubiquinone-enriched mitochondrial membranes | Q72940609 | ||
| Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndrome | Q93673454 | ||
| P433 | issue | 2 | |
| P921 | main subject | Kearns-Sayre syndrome | Q2605012 |
| P304 | page(s) | 97-101 | |
| P577 | publication date | 1989-02-01 | |
| P1433 | published in | Journal of Neurology | Q6295649 |
| P1476 | title | Coenzyme Q in serum and muscle of 5 patients with Kearns-Sayre syndrome and 12 patients with ophthalmoplegia plus | |
| P478 | volume | 236 |
| Q41048491 | A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency. |
| Q42872025 | A randomized trial of coenzyme Q10 in mitochondrial disorders |
| Q37949497 | Co-enzyme Q10: a new drug for cardiovascular disease |
| Q36443232 | Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes |
| Q37708105 | Coenzyme Q10 deficiencies in neuromuscular diseases |
| Q41601393 | Defects in the mitochondrial energy metabolism outside the respiratory chain and the pyruvate dehydrogenase complex |
| Q37901947 | Defects of the respiratory chain. |
| Q68146270 | Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia |
| Q28201358 | Endocrine dysfunction in Kearns-Sayre syndrome |
| Q72674877 | Improvement of refractory sideroblastic anaemia with ubidecarenone |
| Q35038630 | Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features |
| Q67895429 | Muscle coenzyme Q10 in mitochondrial encephalomyopathies |
| Q69354024 | Partial deficiency of complexes I and IV of the mitochondrial respiratory chain in skeletal muscle of two patients with mitochondrial myopathy |
| Q73429199 | Plasma coenzyme Q10 reference intervals, but not redox status, are affected by gender and race in self-reported healthy adults |
| Q37944567 | Primary and secondary CoQ(10) deficiencies in humans |
| Q41180888 | The treatment of congenital lactic acidoses |
| Q40898218 | Treatment of mitochondrial disease |
| Q68244362 | Ultrastructural abnormalities of mitochondria and deficiency of myocardial cytochrome c oxidase in a patient with ventricular tachycardia |
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