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ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.

作者信息

ALEU F P, TERRY R D, ZELLWEGER H

出版信息

J Neuropathol Exp Neurol. 1965 Apr;24:304-17. doi: 10.1097/00005072-196504000-00010.

DOI:10.1097/00005072-196504000-00010
PMID:14280504
Abstract
摘要

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ELECTRON MICROSCOPY OF TWO CEREBRAL BIOPSIES IN GARGOYLISM.黏多糖贮积症Ⅱ型患者两份脑活检组织的电子显微镜检查
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ULTRASTRUCTURAL AND BIOCHEMICAL OBSERVATIONS ON A CASE OF SYSTEMIC LATE INFANTILE LIPIDOSIS AND ITS RELATIONSHIP TO TAY-SACHS DISEASE AND GARGOYLISM.一例全身性晚发性婴儿脂质沉积症的超微结构及生化观察及其与泰-萨克斯病和黏多糖贮积症的关系
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STRUCTURE COMPARISON OF THE MAJOR MONOSIALOGANGLIOSIDES FROM BRAINS OF NORMAL HUMAN, GARGOYLISM, AND LATE INFANTILE SYSTEMIC LIPIDOSIS. I.正常人类、黏多糖贮积症和晚期婴儿全身性脂质沉积症患者大脑中主要单唾液酸神经节苷脂的结构比较。I.
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FORMATION OF THE MEMBRANOUS CYTOPLASMIC BODIES IN TAY-SACHS DISEASE: AN IN VITRO STUDY.泰-萨克斯病中膜性细胞质小体的形成：一项体外研究
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[ULTRASTRUCTURE OF THE HEPATIC CELLS IN HURLER'S DISEASE (GARGOYLISM)].[黏多糖贮积症Ⅰ型（承霤病）肝细胞的超微结构]
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Arch Dis Child. 1964 Dec;39(208):634-40. doi: 10.1136/adc.39.208.634.
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STAINING OF ISOLATED ABNORMAL NEURONAL CYTOSOMES.分离出的异常神经元胞体的染色
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G5-ganglioside variant of systemic late infantile lipidosis. Generalized gangliosidosis.全身性晚发性婴儿脂质沉积症的 G5-神经节苷脂变体。全身性神经节苷脂沉积症。
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Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry.黏多糖贮积症的胡勒氏型和桑菲利普氏型。脑病理学与脂质化学。
Arch Pathol. 1971 May;91(5):434-43.

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Virchows Arch A Pathol Anat Histol. 1982;394(3):195-205. doi: 10.1007/BF00430665.
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