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The liver in generalized glycogen storage disease. Light microscopic observations.

作者信息

McAdams A J, Wilson H E

出版信息

Am J Pathol. 1966 Jul;49(1):99-111.

PMID:5222016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1916462/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/c15a5d677f75/amjpathol00272-0119-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/995a44d4660b/amjpathol00272-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/a43dbabcd8e2/amjpathol00272-0117-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/c15a5d677f75/amjpathol00272-0119-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/995a44d4660b/amjpathol00272-0115-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/a43dbabcd8e2/amjpathol00272-0117-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1262/1916462/c15a5d677f75/amjpathol00272-0119-a.jpg

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The liver in generalized glycogen storage disease. Light microscopic observations.
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引用本文的文献

1
Lysosomes in type II glycogenosis. Changes during administration of extract from Aspergillus niger.II型糖原贮积病中的溶酶体。黑曲霉提取物给药期间的变化。
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2
Temperature-induced experimental myocardial hypertrophy in chick embryos. An electron-microscopic and chemical study.
Am J Pathol. 1967 Jun;50(6):975-91.

本文引用的文献

1
Glycogen disease resembling mongolism, cretinism, and amytonia congenita; case report and review of literature.
J Pediatr. 1950 Jan;36(1):11-30, illust. doi: 10.1016/s0022-3476(50)80174-9.
2
Glycogen storage disease of the heart. I. Report of 2 cases in siblings with chemical and pathologic studies.心脏糖原贮积病。I. 对一对患此病的同胞兄妹进行化学及病理学研究的2例报告。
Pediatrics. 1950 Sep;6(3):402-24.
3
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.
4
GENERALIZED GLYCOGENOSIS. REPORT OF A CASE WITH DEFICIENCY OF ALPHA GLUCOSIDASE.
J Pediatr. 1964 Aug;65:243-51. doi: 10.1016/s0022-3476(64)80526-6.
5
IDENTIFICATION AND STRUCTURAL FORMS OF HUMAN PARTICULATE GLYCOGEN.人类颗粒糖原的鉴定与结构形式
Lab Invest. 1963 Dec;12:1179-97.
6
Studies in disorders of muscle. IX. Glycogen storage disease primarily affecting skeletal muscle and clinically resembling amyotonia congenita.肌肉疾病研究。IX. 主要影响骨骼肌且临床症状类似先天性肌张力缺失的糖原贮积病。
Pediatrics. 1953 Aug;12(2):165-77.
7
Imbalance of liver phosphorylase and accumulation of hepatic glycogen in a girl with progressive disease of the brain.一名患有进行性脑部疾病的女孩肝脏磷酸化酶失衡与肝糖原积累
J Pediatr. 1965 Nov;67(5):741-51. doi: 10.1016/s0022-3476(65)80362-6.