肌肉肉碱缺乏症。与脂质肌病、空泡性神经病变及空泡化白细胞的关联。 - Suppr

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超能文献

Muscle carnitine deficiency. Association with lipid myopathy, vacuolar neuropathy, and vacuolated leukocytes.

作者信息

Markesbery W R, McQuillen M P, Procopis P G, Harrison A R, Engel A G

出版信息

Arch Neurol. 1974 Nov;31(5):320-4. doi: 10.1001/archneur.1974.00490410068007.

DOI:10.1001/archneur.1974.00490410068007

PMID:4414743

Abstract

摘要

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Muscle carnitine deficiency. Association with lipid myopathy, vacuolar neuropathy, and vacuolated leukocytes.肌肉肉碱缺乏症。与脂质肌病、空泡性神经病变及空泡化白细胞的关联。

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引用本文的文献

Muscle carnitine deficiency: adult onset lipid storage myopathy with sensory neuropathy.肌肉肉碱缺乏症：成人发病脂质贮积性肌病伴感觉性神经病。

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EMG changes in chronically dialyzed uraemic subjects undergoing d, 1-Carnitine treatment.

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l-Carnitine. A preliminary review of its pharmacokinetics, and its therapeutic use in ischaemic cardiac disease and primary and secondary carnitine deficiencies in relationship to its role in fatty acid metabolism.左旋肉碱。对其药代动力学、在缺血性心脏病中的治疗应用以及与脂肪酸代谢作用相关的原发性和继发性肉碱缺乏症的初步综述。

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Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case.

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Autosomal recessive lipid storage myopathy (probable carnitine deficiency).常染色体隐性脂质贮积性肌病（可能为肉碱缺乏症）。

J Med Genet. 1979 Dec;16(6):435-8. doi: 10.1136/jmg.16.6.435.

[Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)].关于肌肉肉碱缺乏症的临床、形态学及生物化学研究（作者译）

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