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

Suppr

超能文献

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/1262/1916462/995a44d4660b/amjpathol00272-0115-a.jpg

相似文献

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

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

Glycogen storage disease type IB.

Arch Pathol Lab Med. 1983 Jun;107(6):283-5.

[A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)].

Arch Fr Pediatr. 1981 Dec;38 Suppl 1:837-41.

[Morphology of the hepatic cell under electron microscopic observation in a case of glycogenosis (Von Gierke's disease)].[糖原贮积症（冯·吉尔克病）一例肝细胞电镜观察的形态学]

Biol Lat. 1959 Apr-Jun;12(2):177-85.

[Differential diagnosis of glycogenoses].[糖原贮积症的鉴别诊断]

Arkh Patol. 1980;42(12):61-71.

Type III glycogenosis with multicore structures.伴有多核结构的III型糖原贮积病。

Muscle Nerve. 1979 Mar-Apr;2(2):124-32. doi: 10.1002/mus.880020207.

[Types of reactions of the liver in the newborn and infants (observations on liver cirrhoses in early childhood)].

Virchows Arch Pathol Anat Physiol Klin Med. 1967;344(4):295-306.

[Pompe's disease or glycogen storage disease].

Duodecim. 1982;98(9):709-16.

Type IV glycogen storage disease: first reported case in Thailand.

J Med Assoc Thai. 1989 Dec;72(12):697-700.

Type 3 glycogenosis. A biochemical and electron microscopic study.III型糖原贮积病。一项生化与电子显微镜研究。

Lab Invest. 1970 May;22(5):468-77.

引用本文的文献

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。

J Cell Biol. 1967 Oct;35(1):C1-6. doi: 10.1083/jcb.35.1.c1.

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

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.

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.

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.

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.

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.

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.

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.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验