The glycogen storage diseases

No abstract is available for this paper.

• Publication year

  1974

• Venue

  Journal of clinical pathology. Supplement

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  DOI 10.1136/jcp.27.Suppl_8.106PMID 4620884PMCID PMC1347207
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• The second wind phenomenon in McArdle's syndrome.

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• Glucose 6-phosphatase deficiency: Mechanisms of genetic control and biochemistry

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• DEANOL IN SPONTANEOUS AND INDUCED DYSKINESIAS

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• Hepatic phosphorylase deficiency

  1974cited by this paper
• 糖原病 Phosphorylase kinase deficiency の症例(臨床講義)

  1974cited by this paper
• [Type II glycogenosis].

  1974cited by this paper
• The effect of glucagon antibodies on plasma glucose and insulin levels.

  1973cited by this paper
• Glycogen Metabolism of Human Diploid Fibroblast Cells in Culture. I. Studies of Cells from Patients with Glycogenosis Types II, III, and V

  1973cited by this paper
• Platelet dysfunction in glycogen storage disease type I.

  1973cited by this paper
• Endocrinological findings in patients with glycogenosis.

  1973cited by this paper
• [AN AUTOPSY CASE OF GLYCOGEN AND NON‐GLYCOGEN POLYSACCHARIDE STORAGE DISEASE WITH CARDIOMEGALY

  1973cited by this paper
• Hepatic phosphorylase deficiency: a biochemical study.

  1973cited by this paper
• Glycogen phosphorylase kinase deficiency: a survey of enzymes in phosphorylase activating system.

  1973cited by this paper
• TWO AUTOPSY CASES OF GLYCOGEN STORAGE DISEASE ‐CIRRHOTIC TYPE

  1973cited by this paper
• Glycogen storage disease type 3 and diabetes mellitus.

  1972cited by this paper
• [Hepatic glycogenosis without known enzyme deficiency with clinical and biological signs of type I Cori disease].

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• Glycogen storage disease, type 8.

  1972cited by this paper
• GLYCOGEN STORAGE DISEASE IN NORWAY

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• Rodent and human acid -glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosis.

  1972cited by this paper
• Primer activity of a low molecular weight glycogen from a patient with an unusual glycogen storage disease.

  1972influential reference
• Reye's syndrome: relation of outcome to therapy.

  1972cited by this paper
• Separation of phospholipids from glucose-6-phosphatase by gel chromatography. Specificity of phospholipid reactivation.

  1972cited by this paper
• Lysosomal localization of -fructofuranosidase-containing liposomes injected into rats.

  1972cited by this paper
• Ketosis in Hepatic Glycogenosis

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• Histochemical Phosphorylase Activity in Regenerating Muscle Fibers from Myophosphorylase-Deficient Patients

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• Type 3 glycogenosis: atypical enzyme activities in blood cells in two siblings.

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• [A case of glycogenosis with recurrent hypoglycemia without enzymatic deficiency on liver biopsy].

  1972cited by this paper
• Portacaval shunt for glycogen storage disease: value of prolonged intravenous hyperalimentation before surgery.

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• Incidence of glycogen storage disease in Sweden.

  1972cited by this paper
• Glycogenosis. IV. A new cause of infantile hypotonia.

  1972cited by this paper
• Fate of protein-containing liposomes injected into rats. An approach to the treatment of storage diseases.

  1972cited by this paper
• Gross cardiac involvement in glycogen storage disease type 3.

  1972cited by this paper
• Glycogénoses hépatiques sans déficit enzymatique reconnu se comportant cliniquement et biologiquement comme le type I de Cori.

  1972cited by this paper
• Hepatic Glycogen Synthetase Deficiency

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• GLYCOGEN STORAGE DISEASE TYPE III AND DIABETES MELLITUS

  1972cited by this paper
• DYNAMIC STUDIES OF GLYCOGEN METABOLISM IN GLYCOGEN STORAGE DISEASE USING FIBROBLAST CULTURES DERIVED FROM PATIENTS AND THEIR FAMILIES

  1972cited by this paper
• THE TURNOVER OF (2- 3 H) GLUCOSE: AN ASSAY FOR DIAGNOSIS OF TYPE I GLYCOGENOSIS

  1972cited by this paper
• Different properties of glucose-6-phosphatase and related enzymes in rough and smooth endoplasmic reticular membranes.

  1971cited by this paper
• Ultrastructure and Enzymatic Deficiency of Fibroblast Cultures in Type II Glycogenosis

  1971cited by this paper
• Immunological studies on glycogen storage diseases type 3 and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency.

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• Hepatic glycogenosis due to phosphorylase deficiency. Limitations of enzyme studies on liver biopsy specimens.

  1971cited by this paper
• New aspects of glycogen metabolism.

  1971cited by this paper
• Hepatic glycogen storage disease. Clinical and laboratory findings in 23 cases.

  1971cited by this paper
• Alpha-1,4 glucosidase activity in Pompe's disease.

  1971cited by this paper
• Enzymes of glycogen metabolism in human skin with particular reference to differential diagnosis of the glycogen storage diseases.

  1971cited by this paper
• Enzyme entrapment in liposomes

  1971cited by this paper
• Type 3 glycogenosis. An adult with diffuse weakness and muscle wasting.

  1971cited by this paper
• Glycogenosis type I (glucose 6-phosphatase deficiency): ultrastructural alterations of hepatocytes in a tumor bearing liver

  1971cited by this paper
• Loss of cyclic 3'5'-AMP dependent kinase and reduction of phosphorylase kinase in skeletal muscle of a girl with deactivated phosphorylase and glycogenosis of liver and muscle.

  1970cited by this paper
• Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies.

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• Portacaval shunt in the treatment of glycogen storage disease: Report of a case : R. E. Hermann and R. D. Mercer. Surgery 65:499–503, (March) 1969

  1970cited by this paper
• Prenatal diagnosis of type-II glycogenosis.

  1970cited by this paper
• A revision of the Meyer‐Bernfeld model of glycogen and amylopectin

  1970cited by this paper
• Phosphorylase kinase deficiency

  1970cited by this paper
• Type IV glycogenosis (amylopectinosis). Light and electron microscopic observations.

  1970cited by this paper
• The fine structure of glycogen from type IV glycogen-storage disease.

  1970cited by this paper
• Treatment of eruptive xanthomas in Cori type I glycogenosis.

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• FINE‐NEEDLE ASPIRATION BIOPSY OF HUMAN LIVER FOR ENZYMATIC DIAGNOSIS OF GLYCOGEN STORAGE DISEASE AND GARGOYLISM

  1970cited by this paper
• Hyperlipidemia in type 3 glycogenosis.

  1970cited by this paper
• HYPERLIPIDEMIA IN TYPE III GLYCOGENOSIS

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• GENETIC STUDIES IN GLYCOGEN STORAGE DISEASE TYPE III

  1970cited by this paper
• Liver glycogenosis and phosphorylase kinase deficiency.

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• Branching action of amylo‐1,6‐glucosidase/oligo‐1,4→1,4‐glucantransferase

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• Glycogen-storage disease Type VIa: low phosphorylase kinase activity caused by a low enzyme-substrate affinity.

  1970cited by this paper
• A screening method for liver glycogen diseases.

  1969cited by this paper
• Deficient activity of dephosphophosphorylase kinase and accumulation of glycogen in the liver.

  1969cited by this paper
• Growth in glycogen-storage disease type 1. Evaluation of endocrine function.

  1969cited by this paper
• In-utero detection of type-II glycogenosis (pompe's disease).

  1969cited by this paper
• Portacaval shunt in the treatment of glycogen storage disease: report of a case.

  1969cited by this paper
• Glycogen storage diseases

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• Portacaval shunt in the treatment of glycogen storage disease: report of a case.

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• Insulin Secretion in Type I Glycogen Storage Disease

  1969cited by this paper
• Hyperlipemia in children with liver glycogen disease.

  1969cited by this paper
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  1969cited by this paper
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• Studies in glycogen storage disease

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• Administration of a mixture of fungal glucosidases to a patient with type II glycogenosis (Pompe's disease).

  1968cited by this paper
• McArdle's disease: lack of muscle phosphorylase.

  1968cited by this paper
• Glycogen storage disease type IV, amylopectinosis.

  1968cited by this paper
• Occasional Survey: THE MUSCLE GLYCOGENOSES

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• A TECHNIQUE FOR THE ENZYMATIC DIAGNOSIS OF GLYCOGEN STORAGE DISEASE ON VERY SMALL TISSUE SPECIMENS

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  1968cited by this paper
• Adult myopathy from glycogen storage disease due to acid maltase deficiency.

  1968cited by this paper
• A technique for the enzymatic diagnosis of glycogen storage disease on very small tissue specimens.

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• Contracture of phosphorylase deficient muscle.

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• The muscle glycogenoses.

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• Branching enzyme-deficiency glycogenosis: studies in therapy.

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• Studies in glycogen storage disease. 3. Limit dextrinosis: a genetic study.

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• Excessive production of uric acid in type I glycogen storage disease.

  1968cited by this paper
• Glycogen-Storage Diseases: Types I, III, IV, V, VII and Unclassified Glycogenoses

  1968cited by this paper
• Hexose and protein tolerance tests in children with liver glycogenosis caused by a deficiency of the debranching enzyme system.

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• Glycogen-Storage Diseases: Type II and Type VI Glycogenosis

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• McArdle's Disease: Lack of Muscle Phosphorylase

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• Retinal changes in glycogen storage disease type I.

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