Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations.

作者信息

Schochet S S, McCormick W F, Zellweger H

出版信息

Arch Pathol. 1970 Oct;90(4):354-63.

PMID:5272555

Abstract

摘要

相似文献

Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations.

Arch Pathol. 1970 Oct;90(4):354-63.

Light and electron microscopy of skeletal muscle in type IV glycogenosis.

Acta Neuropathol. 1971;19(2):137-44. doi: 10.1007/BF00688492.

Demonstration of glycogen in glycogenosis types 1, 2 and 4.

J Med Lab Technol. 1970 Jan;27(1):43-8.

[Histochemical study on skin culture in type II glycogenosis].

Riv Anat Patol Oncol. 1968;33:520-3.

Type 3 glycogenosis. A biochemical and electron microscopic study.

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

Glycogen storage disease type IB.

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

Fine structure of skeletal muscle in type-3 glycogenosis.

Arch Pathol. 1969 Aug;88(2):130-6.

[Electron microscopic study of liver and muscles in two cases of type 3 glycogenosis].

Pathol Eur. 1972;7(2):112-25.

Type III glycogenosis with multicore structures.

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

[Glycogenosis due to amylo-1-6-glucosidase deficiency associated with a disorder thyroid hormone synthesis].

Arch Fr Pediatr. 1971 Aug-Sep;28(7):699-709.

引用本文的文献

Late-onset polyglucosan body myopathy in five patients with a homozygous mutation in GYG1.

Neuromuscul Disord. 2016 Jan;26(1):16-20. doi: 10.1016/j.nmd.2015.10.012. Epub 2015 Nov 10.

Increased laforin and laforin binding to glycogen underlie Lafora body formation in malin-deficient Lafora disease.

J Biol Chem. 2012 Jul 20;287(30):25650-9. doi: 10.1074/jbc.M111.331611. Epub 2012 Jun 5.

Unclassified polysaccharidosis of the heart and skeletal muscle in siblings.

Mol Genet Metab. 2008 Sep-Oct;95(1-2):52-8. doi: 10.1016/j.ymgme.2008.07.005. Epub 2008 Aug 8.

Biochemical characterization of a neuroserpin variant associated with hereditary dementia.

Am J Pathol. 2001 Jan;158(1):227-33. doi: 10.1016/S0002-9440(10)63961-2.

Familial encephalopathy with neuroserpin inclusion bodies.

Am J Pathol. 1999 Dec;155(6):1901-13. doi: 10.1016/S0002-9440(10)65510-1.

Liver transplantation for type I and type IV glycogen storage disease.

Eur J Pediatr. 1993;152 Suppl 1(Suppl 1):S71-6. doi: 10.1007/BF02072093.

Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).

Acta Neuropathol. 1993;85(4):419-30. doi: 10.1007/BF00334454.

Hepatic ultrastructure in leprechaunism. Hepatic ultrastructural evidence suggesting a syndrome with defective hepatic glucose release.

Virchows Arch A Pathol Anat Histol. 1982;397(2):121-30. doi: 10.1007/BF00442383.

Polyglucosan bodies in the digestive tract of the aged dog.

Acta Neuropathol. 1983;60(3-4):297-300. doi: 10.1007/BF00691880.

Teaching monograph: pathology of skeletal muscle diseases.

Am J Pathol. 1982 May;107(2):231-76.

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