| scholarly article | Q13442814 |
| P2093 | author name string | Takemoto M | |
| Yamamoto M | |||
| Sato T | |||
| Ujike H | |||
| Anno M | |||
| P2860 | cites work | Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome | Q28259574 |
| Nondroplet ultrastructural demonstration of cytochrome oxidase activity with a polymerizing osmiophilic reagent, diaminobenzidine (DAB). | Q36189741 | ||
| Kearns-Sayre syndrome with reduced plasma and cerebrospinal fluid folate | Q42465478 | ||
| Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia | Q45894329 | ||
| A mitochondrial myopathy characterized by a deficiency in reducible cytochrome b. | Q48246628 | ||
| Mitochondrial encephalomyopathies: a group of neuromuscular disorders with defects in oxidative metabolism | Q48315163 | ||
| Mitochondrial encephalomyopathy: fluctuating symptoms and CT. | Q48606569 | ||
| Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase? | Q48710613 | ||
| A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia. | Q51646557 | ||
| Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle | Q67271350 | ||
| Treatment of Kearns-Sayre syndrome with coenzyme Q10 | Q69991702 | ||
| Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis | Q70599228 | ||
| A rapid method for the preparation of highly purified cytochrome oxidase | Q79543798 | ||
| [Mitochondrial encephalomyopathy: a case with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)] | Q93594770 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | ubidecarenone | Q321285 |
| lactic acidosis | Q1500373 | ||
| mitochondrial myopathy | Q6881881 | ||
| P304 | page(s) | 1475-1481 | |
| P577 | publication date | 1987-11-01 | |
| P1433 | published in | Journal of Neurology, Neurosurgery and Psychiatry | Q1599804 |
| P1476 | title | Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration | |
| P478 | volume | 50 |
| Q42872025 | A randomized trial of coenzyme Q10 in mitochondrial disorders |
| Q53343108 | Advances in the Treatment of MELAS Syndrome: Could Cognitive Rehabilitation Have a Role? |
| Q90330689 | Causes of low muscle coenzyme-Q levels beyond primary coenzyme-Q-deficiency |
| Q38114007 | Coenzyme Q10 depletion in medical and neuropsychiatric disorders: potential repercussions and therapeutic implications |
| Q44826636 | Cofactor treatment improves ATP synthetic capacity in patients with oxidative phosphorylation disorders |
| Q34069102 | Diagnosis of rare dementia syndromes: an algorithmic approach |
| Q36315564 | Digestive smooth muscle mitochondrial myopathy in patients with mitochondrial-neuro-gastro-intestinal encephalomyopathy (MNGIE). |
| Q48173034 | Evidence of altered energy metabolism in autistic children |
| Q77736764 | Familial occurrence of intestinal obstruction in children with the syndrome of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) |
| Q79794045 | Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD) |
| Q44937716 | Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies |
| Q71509055 | Metabolic myopathies |
| Q78517318 | Mitochondrial diseases |
| Q35038630 | Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features |
| Q28251780 | Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts |
| Q67895429 | Muscle coenzyme Q10 in mitochondrial encephalomyopathies |
| Q42288275 | Myopathy in long-term AZT therapy: clinical, electrophysiological and biopsy study in 67 HIV+ subjects |
| Q34218646 | Nutritional cofactor treatment in mitochondrial disorders |
| Q71841152 | Riboflavin-responsive complex I deficiency |
| Q34312609 | Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy |
| Q48752106 | Stroke-like episodes in familial mitochondrial encephalomyopathy: clinical and biochemical aspects |
| Q81351127 | The "S" in MELAS |
| Q48787948 | Unusual occurrence of intestinal pseudo obstruction in a patient with maternally inherited diabetes and deafness (MIDD) and favorable outcome with coenzyme Q10. |
| Q92446351 | Urogenital symptoms in mitochondrial disease: overlooked and undertreated |
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