[神经肌肉性糖原贮积病（II型）中骨骼肌黏多糖样物质（嗜碱性物质）的组织化学] - Suppr

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超能文献

[Histochemistry of mucopolysaccharide-like substances (basophilic substances) in skeletal muscle in neuromuscular glycogenosis (type II)].

作者信息

Schnabel R

出版信息

Acta Neuropathol. 1971;17(2):169-78. doi: 10.1007/BF00687492.

DOI:10.1007/BF00687492

PMID:5544569

Abstract

摘要

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[Histochemistry of mucopolysaccharide-like substances (basophilic substances) in skeletal muscle in neuromuscular glycogenosis (type II)].[神经肌肉性糖原贮积病（II型）中骨骼肌黏多糖样物质（嗜碱性物质）的组织化学]

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引用本文的文献

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.

本文引用的文献

Glycogenosis type II.

Arch Pathol. 1967 Aug;84(2):141-52.

Glycogen disease of skeletal muscle; report of two cases and review of literature.骨骼肌糖原贮积病；两例报告及文献复习

Pediatrics. 1955 Jun;15(6):715-32.

[PATHOGENESIS AND DIFFERENTIAL DIAGNOSIS OF GLYCOGENOSES].[糖原贮积病的发病机制与鉴别诊断]

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INBORN LYSOSOMAL DISEASES.先天性溶酶体病

Gastroenterology. 1965 May;48:625-33.

POMPE'S DISEASE (DIFFUSE GLYCOGENOSIS) WITH NEURONAL STORAGE.庞贝氏病（弥漫性糖原贮积症）伴神经元贮积

J Neuropathol Exp Neurol. 1965 Jan;24:85-96. doi: 10.1097/00005072-196501000-00008.

OCULAR HISTOPATHOLOGY IN GENERALIZED GLYCOGENOSIS (POMEPE'S DISEASE).全身性糖原贮积病（庞贝氏病）的眼部组织病理学

Arch Ophthalmol. 1965 Mar;73:342-9. doi: 10.1001/archopht.1965.00970030344009.

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AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS.II型糖原贮积病的电子显微镜及生化研究

Lab Invest. 1964 Sep;13:1139-52.

[STUDY OF 2 CASES OF GENERALIZED GLYCOGENOSIS WITH CARDIOMEGALY (POMPE'S DISEASE)].

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