Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
about
Mitochondrial myopathy: a genetic study of 71 casesMitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosisMitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current conceptsUpdate on chronic progressive external ophthalmoplegia.Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model.Exercise intolerance, lactic acidosis, and abnormal cardiopulmonary regulation in exercise associated with adult skeletal muscle cytochrome c oxidase deficiency.Chronic intestinal pseudoobstruction and ophthalmoplegia in a patient with mitochondrial myopathyBilateral lid/brow elevation procedure for severe ptosis in Kearns-Sayre syndrome, a mitochondrial cytopathy.Megamitochondria formation - physiology and pathology.Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.Gyrate atrophy of the choroid and retina with hyperornithinemia: biochemical and histologic studies and response to vitamin B6The molecular era of myology.Peripheral neuropathy associated with mitochondrial myopathy.Skeletal muscle pathology in chronic heart block.Ultrastructural examination of the skeletal muscles in polymyalgia rheumatica."Mitochondrial myopathy" or mitochondrial disease? EEG, ERG, VEP studies in 13 childrenNeurological associations of chronic heart blockCongenital myasthenia gravis: clinical and HLA studies in two brothers.Mitochondria-related encephalomyopathies.Oculopharyngeal myopathy with distal and cardiomyopathy.[Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study.Electromyography in infants and children.Chick muscle in tissue culture: the ubiquity of viral infection.Hyperglycemic acidotic coma and death in Kearns-Sayre syndrome.Mitochondrial myopathies. Clinical, morphological and biochemical aspects.Historical and current concepts in mitochondrial myopathies.Pathology of skeletal muscle: principles of reaction patterns and histochemistry and experience with 195 biopsies.Congenital myopathy with progressive external ophthalmoplegia.Ocular myopathy (progressive external ophthalmoplegia) with neuropathic complications.Muscular dystrophy in a litter of golden retriever dogs.Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?Myocardial ultrastructure in Kearns-Sayre syndrome.Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS): adolescent onset with severe cerebral edema.Cryptic disseminated tuberculosis presenting as gaze palsy.Multimodal evoked potentials in progressive external ophthalmoplegia with mitochondrial myopathy.Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism.General anesthesia for progressive external ophthalmoplegia syndrome.Cerebral nuclear magnetic resonance (MRI) in Kearns syndrome.
P2860
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P2860
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
description
1972 nî lūn-bûn
@nan
1972年の論文
@ja
1972年学术文章
@wuu
1972年学术文章
@zh
1972年学术文章
@zh-cn
1972年学术文章
@zh-hans
1972年学术文章
@zh-my
1972年学术文章
@zh-sg
1972年學術文章
@yue
1972年學術文章
@zh-hant
name
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@en
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@nl
type
label
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@en
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@nl
prefLabel
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@en
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@nl
P2093
P1433
P1476
Oculocraniosomatic neuromuscular disease with "ragged-red" fibers.
@en
P2093
P304
P356
10.1001/ARCHNEUR.1972.00490090019001
P577
1972-03-01T00:00:00Z