scholarly article | Q13442814 |
P356 | DOI | 10.1002/ANA.410330308 |
P953 | full work available at URL | https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fana.410330308 |
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ana.410330308 | ||
P698 | PubMed publication ID | 7684581 |
P2093 | author name string | M. Tokunaga | |
S. Araki | |||
S. Mita | |||
I. Nonaka | |||
R. Sakuta | |||
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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity | Q26778490 | ||
Sequence and organization of the human mitochondrial genome | Q27860659 | ||
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome | Q28259574 | ||
Retinitis Pigmentosa, External Ophthalmoplegia, and Complete Heart Block | Q30053138 | ||
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation | Q34152888 | ||
Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome | Q34323823 | ||
Myoclonus epilepsy associated with ragged-red fibres (mitochondrial abnormalities ): disease entity or a syndrome? Light-and electron-microscopic studies of two cases and review of literature | Q34712806 | ||
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNA. | Q35907687 | ||
Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes | Q36811500 | ||
Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes | Q41910533 | ||
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation | Q43518868 | ||
A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). | Q44484780 | ||
Impairment of mitochondrial transcription termination by a point mutation associated with the MELAS subgroup of mitochondrial encephalomyopathies | Q46081296 | ||
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome | Q46963412 | ||
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies | Q48836050 | ||
Deletion mutants are functionally dominant over wild-type mitochondrial genomes in skeletal muscle fiber segments in mitochondrial disease | Q48933491 | ||
A partial deficiency of cytochrome c oxidase in chronic progressive external ophthalmoplegia. | Q51646557 | ||
Vascular involvement in mitochondrial myopathy. | Q52065483 | ||
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RAPID EXAMINATION OF MUSCLE TISSUE. AN IMPROVED TRICHROME METHOD FOR FRESH-FROZEN BIOPSY SECTIONS | Q76607062 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | lactic acidosis | Q1500373 |
mitochondrial myopathy | Q6881881 | ||
P304 | page(s) | 275-280 | |
P577 | publication date | 1993-03-01 | |
P1433 | published in | Annals of Neurology | Q564414 |
P1476 | title | Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) | |
Increased mitochondrial DNA in blood vessels and ragged‐red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke‐like episodes (MELAS) | |||
P478 | volume | 33 |
Q49143394 | Assessment of the distribution of mitochondrial ribosomal RNA in melas and in thrombotic cerebral infarcts by in situ hybridization |
Q82454694 | Carotid dissection in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes |
Q48429272 | Cerebral blood flow and oxygen metabolism before and after a stroke-like episode in patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). |
Q37623186 | Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers. |
Q36686802 | Genotype-phenotype correlation of maternally inherited disorders due to mutations in mitochondrial DNA. |
Q40607631 | Humanin improves impaired metabolic activity and prolongs survival of serum-deprived human lymphocytes |
Q40396328 | Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle |
Q35889709 | Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene |
Q35986703 | Microangiopathy in the cerebellum of patients with mitochondrial DNA disease |
Q71852965 | Mitochondrial DNA mutation and muscle pathology in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes |
Q38570577 | Mitochondrial dysfunction and seizures: the neuronal energy crisis |
Q35707204 | Neuropathological aspects of mitochondrial DNA disease |
Q36318499 | Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesis |
Q34738513 | On the molecular etiology of decreased arachidonic (20:4n-6), docosapentaenoic (22:5n-6) and docosahexaenoic (22:6n-3) acids in Zellweger syndrome and other peroxisomal disorders |
Q38668918 | Simultaneous A8344G heteroplasmy and mitochondrial DNA copy number quantification in myoclonus epilepsy and ragged-red fibers (MERRF) syndrome by a multiplex molecular beacon based real-time fluorescence PCR. |
Q35790038 | Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease |
Q74419457 | Single muscle fiber analysis of myoclonus epilepsy with ragged-red fibers |
Q26777744 | When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis? |
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