Home LiteratureArticle Details
PMID: 4114291 Published · ppublish English Journal Article Review

The histochemical evaluation of the glycogen storage diseases. A review of techniques and their limitations.

The Histochemical journal ·Vol. 2 ·No. 5 ·1970-09-00 ·Pages 441-50

Lake BD

Abstract

暂无摘要

MeSH Terms
Biopsy Glucose-6-Phosphatase/analysis Glucosephosphate Dehydrogenase Deficiency/enzymology Glucosidases/analysis Glucosyltransferases/analysis Glycogen/analysis Glycogen Storage Disease/enzymology,metabolism,pathology Histocytochemistry Humans Lipids/analysis Liver/enzymology,pathology Liver Glycogen/analysis Muscle, Smooth/analysis,enzymology,pathology Phosphoglucomutase/analysis Staining and Labeling
Chemicals
Lipids Liver Glycogen Glycogen Glucosyltransferases Glucose-6-Phosphatase Glucosidases Phosphoglucomutase
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Lake B D
References (27)
27 references, click to expand
  1. PHOSPHOFRUCTOKINASE DEFICIENCY IN SKELETAL MUSCLE. A NEW TYPE OF GLYCOGENOSIS.
    Biochem Biophys Res Commun. 1965 May 3;19:517-23 PMID: 14339001
  2. Demonstration of glycogen in glycogenosis types 1, 2 and 4.
    J Med Lab Technol. 1970 Jan;27(1):43-8 PMID: 4904713
  3. The role of histochemical and biochemical preparation methods for the detection of glycogen.
    J Histochem Cytochem. 1969 Aug;17(8):527-38 PMID: 4307897
  4. Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.
    Proc Natl Acad Sci U S A. 1966 Aug;56(2):725-9 PMID: 5229990
  5. Improved localization of phosphorylase by the use of polyvinyl pyrrolidone and high substrate concentration.
    J Histochem Cytochem. 1961 Sep;9:585 PMID: 13890475
  6. Histopathology of McArdle's disease in a family.
    J Pathol Bacteriol. 1967 Oct;94(2):293-300 PMID: 6066477
  7. alpha-Glucosidase deficiency in generalized glycogenstorage disease (Pompe's disease).
    Biochem J. 1963 Jan;86:11-6 PMID: 13954110
  8. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle.
    J Clin Invest. 1959 Nov;38:2044-58 PMID: 14442994
  9. A CASE OF MCARDLE'S SYNDROME WITH A POSITIVE FAMILY HISTORY.
    J Neurol Neurosurg Psychiatry. 1964 Jun;27:186-97 PMID: 14175283
  10. Histochemical diagnosis of muscle phosphofructokinase deficiency.
    Arch Neurol. 1970 Jan;22(1):8-12 PMID: 4243256
  11. Histochemical studies on phosphorylase and amylo 1,4 lead to 1,6-transglucosidase activity in the liver. II. The relationship of glycogen structure to diffusion during histochemical incubation.
    J Med Lab Technol. 1970 Oct;27(4):457-61 PMID: 4992538
  12. Skeletal muscle glycogenosis: an investigation of two dissimilar cases.
    J Neurol Neurosurg Psychiatry. 1963 Feb;26:60-8 PMID: 13981250
  13. Deficient activity of dephosphophosphorylase kinase and accumulation of glycogen in the liver.
    J Clin Invest. 1969 Apr;48(4):704-15 PMID: 5774108
  14. Histochemical Method for the Detection of Phosphorylase in Plant Tissues.
    Science. 1947 Jun 20;105(2738):650 PMID: 17820075
  15. Type IV glycogenosis. Patient with absence of a branching enzyme alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyl transferase.
    Lab Invest. 1968 Nov;19(5):546-57 PMID: 5247008
  16. CYTOLOGICAL PHOSPHORYLASE LOCATIONS IN RAT LIVER AND MUSCLE AS SHOWN BY A LEAD PRECIPITATION METHOD.
    Stain Technol. 1964 Sep;39:275-8 PMID: 14211197
  17. Histochemical method for the demonstration of the activity of phosphoglucomutase.
    Histochemie. 1967;8(3):248-51 PMID: 4386157
  18. [Enzymatic studies of hepatic fragments; application to the classification of glycogenoses].
    Rev Int Hepatol. 1959;9(1):35-55 PMID: 13646331
  19. Propylene and ethylene glycol as solvents for Sudan IV and Sudan black B.
    Stain Technol. 1951 Jan;26(1):51-6 PMID: 14809507
  20. Polysaccharide synthesis in frozen tissue sections as a histochemical method for phosphorylase.
    J Natl Cancer Inst. 1952 Oct;13(2):543-57 PMID: 12991055
  21. GLYCOGEN STORAGE DISEASE.
    Adv Metab Disord. 1964;13:1-44 PMID: 14171618
  22. GLYCOGENOSIS TYPE 1 (LACK OF GLUCOSE-6-PHOSPHATASE) IN FOUR SIBLINGS.
    Acta Paediatr. 1964;58:SUPPL 157:1-28 PMID: 14171870
  23. Histochemical detection of phosphorylase in animal tissues.
    J Histochem Cytochem. 1955 May;3(3):153-60 PMID: 14381604
  24. Enzymorphologic demonstration of glucose 6-phosphate--dependent glycogen synthetase in mouse liver.
    J Histochem Cytochem. 1966 Mar;14(3):247-53 PMID: 5944353
  25. Infantile Hypoglycaemia due to Inherited Deficiency of Glycogen Synthetase in Liver.
    Arch Dis Child. 1963 Feb;38(197):40-8 PMID: 21032403
  26. Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations.
    Mayo Clin Proc. 1968 Apr;43(4):233-79 PMID: 4886322
  27. The subgroups of type 3 glycogenosis.
    Eur J Biochem. 1967 Oct;2(3):265-70 PMID: 5235982
Article Info
Journal
The Histochemical journal
Abbr.
Histochem J
ISSN
0018-2214
DOI
10.1007/BF01004725
Published
1970-09-00
Pages
441-50
Language
English
Region
Netherlands
NLM ID
0163161
Subset
IM
External Links
PubMed source DOI: 10.1007/BF01004725
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com

Copyright © 2026.Genelibs Jinan Honghui Biotechnology Co., Ltd. 鲁ICP备20007159号-2