II型糖原贮积病（庞贝病）：周围神经的超微结构 - Suppr

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超能文献

Glycogenosis type II (Pompe's disease): ultrastructure of peripheral nerves.

作者信息

Araoz C, Sun C N, Shenefelt R, White H J

出版信息

Neurology. 1974 Aug;24(8):739-42. doi: 10.1212/wnl.24.8.739.

DOI:10.1212/wnl.24.8.739

PMID:4526421

Abstract

摘要

相似文献

Glycogenosis type II (Pompe's disease): ultrastructure of peripheral nerves.II型糖原贮积病（庞贝病）：周围神经的超微结构

Neurology. 1974 Aug;24(8):739-42. doi: 10.1212/wnl.24.8.739.

Nervous system in Pompe's disease. Ultrastructure and biochemistry.

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Electron microscopy of ocular muscle in type II glycogenosis (Pompe's disease).

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Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.

Acta Neuropathol. 1973 Feb 19;23(3):229-44. doi: 10.1007/BF00687878.

Properties of the alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease).与II型糖原贮积病（庞贝氏病）相关的来自各种人体组织的α-葡萄糖苷酶的特性

Clin Chim Acta. 1977 Aug 1;78(3):473-8. doi: 10.1016/0009-8981(77)90080-8.

Morphological changes in muscle tissue of patients with infantile Pompe's disease receiving enzyme replacement therapy.接受酶替代疗法的婴儿型庞贝病患者肌肉组织的形态学变化。

Muscle Nerve. 2003 Jun;27(6):743-51. doi: 10.1002/mus.10381.

Administration of a mixture of fungal glucosidases to a patient with type II glycogenosis (Pompe's disease).向一名患有II型糖原贮积病（庞贝氏病）的患者施用真菌糖苷酶混合物。

Pediatrics. 1968 Oct;42(4):672-6.

Pompe's disease.庞贝氏病

Neurology. 1969 Sep;19(9):894-900. doi: 10.1212/wnl.19.9.894.

Glycogen storage disease type II (Pompe's disease): the first biochemical evidence in Thailand.糖原贮积病II型（庞贝氏病）：泰国的首例生化证据。

J Med Assoc Thai. 1987 Sep;70(9):536-42.

[Glycogenosis type II (Pompe's disease) associated with alpha-amylase and hyaluronidase deficiency].[与α-淀粉酶和透明质酸酶缺乏相关的II型糖原贮积病（庞贝病）]

Dtsch Med Wochenschr. 1969 Jul 4;94(27):1414-6. doi: 10.1055/s-0028-1110271.

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Ultrastructural and diffusion tensor imaging studies reveal axon abnormalities in Pompe disease mice.超微结构和弥散张量成像研究显示庞贝病小鼠存在轴突异常。

Sci Rep. 2020 Nov 19;10(1):20239. doi: 10.1038/s41598-020-77193-w.

Postmortem Findings and Clinical Correlates in Individuals with Infantile-Onset Pompe Disease.婴儿型庞贝病患者的尸检结果与临床关联

JIMD Rep. 2015;23:45-54. doi: 10.1007/8904_2015_426. Epub 2015 Mar 13.

Non-muscle involvement in late-onset glycogenosis II.晚发型糖原贮积症II型中的非肌肉受累情况

Acta Myol. 2013 Oct;32(2):91-4.

Temporal neuropathologic and behavioral phenotype of 6neo/6neo Pompe disease mice.6neo/6neo型庞贝病小鼠的颞叶神经病理学和行为表型

J Neuropathol Exp Neurol. 2008 Aug;67(8):803-18. doi: 10.1097/NEN.0b013e3181815994.

Ultrastructural investigations of peripheral nerves in neuronal ceroid-lipofuscinoses (NCL).神经元蜡样脂褐质沉积症（NCL）中周围神经的超微结构研究。

J Neurol. 1976 Oct 4;213(4):295-303. doi: 10.1007/BF00316269.

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