Results 161 to 170 of about 80,863 (210)
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Gout and Glycogen Storage Disease
Annals of Internal Medicine, 1963Excerpt A brother and 2 sisters, known from childhood to have had glycogen storage disease of the liver (Von Gierke's disease), survived to adult life. The course of their disorder was followed.
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Paediatrics and Child Health, 2011
Glycogen storage disorders are a group of inborn errors of metabolism characterized by accumulation of glycogen in various tissues. This accumulation is the histological hallmark of these disorders although the phenotype shows variable overlap. Hepatomegaly, hypoglycaemia, elevated lactate and urate with or without neutrophil dysfunction is the ...
Christian J. Hendriksz, Paul Gissen
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Glycogen storage disorders are a group of inborn errors of metabolism characterized by accumulation of glycogen in various tissues. This accumulation is the histological hallmark of these disorders although the phenotype shows variable overlap. Hepatomegaly, hypoglycaemia, elevated lactate and urate with or without neutrophil dysfunction is the ...
Christian J. Hendriksz, Paul Gissen
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The Journal of Pediatrics, 1945
Summary Two cases of the hepatic form of glycogen storage disease (von Gierke's disease) have been studied in detail. Observations on liver slices freshly removed at biopsy have shown an abnormal stability of the glycogen, but a satisfactory glycogenolytic response was obtained upon admixture with fresh normal liver, confirming previous work that ...
Edward M. Bridge, L. Emmett Holt
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Summary Two cases of the hepatic form of glycogen storage disease (von Gierke's disease) have been studied in detail. Observations on liver slices freshly removed at biopsy have shown an abnormal stability of the glycogen, but a satisfactory glycogenolytic response was obtained upon admixture with fresh normal liver, confirming previous work that ...
Edward M. Bridge, L. Emmett Holt
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Current Paediatrics, 1997
The glycogen storage diseases (GSDs) are an heterogeneous group of inherited disorders of carbohydrate metabolism. The specific enzyme defects are welldefined and for some, current therapeutic interventions are relatively straightforward and effective.
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The glycogen storage diseases (GSDs) are an heterogeneous group of inherited disorders of carbohydrate metabolism. The specific enzyme defects are welldefined and for some, current therapeutic interventions are relatively straightforward and effective.
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2020
Abstract Glycogen is a highly branched glucose polymer with a compacted structure found predominantly in liver and muscle. Liver glycogen is important in the maintenance of euglycaemia during fasting; muscle glycogen is an immediate source of glucose for energy production during exercise.
Robin H. Lachmann, Timothy M. Cox
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Abstract Glycogen is a highly branched glucose polymer with a compacted structure found predominantly in liver and muscle. Liver glycogen is important in the maintenance of euglycaemia during fasting; muscle glycogen is an immediate source of glucose for energy production during exercise.
Robin H. Lachmann, Timothy M. Cox
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Reviews in Endocrine and Metabolic Disorders, 2003
Joseph I, Wolfsdorf, David A, Weinstein
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Joseph I, Wolfsdorf, David A, Weinstein
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Birth defects original article series, 1976
Each of 12 types of glycogen storage disease (GSD O-XI) is delineated by clinical, biochemical and histologic features that allow its identification in future patients. GSD II occurs in 2 forms that are not both encountered in the same family. GSD IIa is the infantile fatal form with cardiomegaly, increased cardiac glycogen concentration and cardiac ...
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Each of 12 types of glycogen storage disease (GSD O-XI) is delineated by clinical, biochemical and histologic features that allow its identification in future patients. GSD II occurs in 2 forms that are not both encountered in the same family. GSD IIa is the infantile fatal form with cardiomegaly, increased cardiac glycogen concentration and cardiac ...
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment
Ca-A Cancer Journal for Clinicians, 2022Jun J Mao,, Msce +2 more
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