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One or more keywords matched the following items that are connected to Wolfsdorf, Joseph
Item TypeName
Academic Article Glycogen storage diseases.
Academic Article Bones benefit from better biochemical control in type 1 glycogen storage disease.
Academic Article Optimal daytime feeding regimen to prevent postprandial hypoglycemia in type 1 glycogen storage disease.
Academic Article Glycogen storage disease type Ia: linkage of glucose, glycogen, lactic acid, triglyceride, and uric acid metabolism.
Academic Article Urinary lactate excretion to monitor the efficacy of treatment of type I glycogen storage disease.
Academic Article Oral sucrose and exercise tolerance in McArdle's disease.
Academic Article Physical growth and development of children with type 1 glycogen-storage disease: comparison of the effects of long-term use of dextrose and uncooked cornstarch.
Academic Article The diagnosis of insulinoma in a child in the absence of fasting hyperinsulinemia.
Academic Article Cornstarch regimens for nocturnal treatment of young adults with type I glycogen storage disease.
Academic Article Metabolic control and renal dysfunction in type I glycogen storage disease.
Academic Article Decreased urinary citrate excretion in type 1a glycogen storage disease.
Academic Article Glycogen storage disease in adults.
Academic Article Continuous glucose for treatment of patients with type 1 glycogen-storage disease: comparison of the effects of dextrose and uncooked cornstarch on biochemical variables.
Academic Article Effect of continuous glucose therapy with uncooked cornstarch on the long-term clinical course of type 1a glycogen storage disease.
Academic Article Effect of continuous glucose therapy begun in infancy on the long-term clinical course of patients with type I glycogen storage disease.
Academic Article Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations.
Academic Article Hepatic glycogen synthase deficiency: an infrequently recognized cause of ketotic hypoglycemia.
Academic Article Glycogen storage diseases. Phenotypic, genetic, and biochemical characteristics, and therapy.
Academic Article Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease.
Academic Article Biochemical evidence for the requirement of continuous glucose therapy in young adults with type 1 glycogen storage disease.
Academic Article Glucose therapy for glycogenosis type 1 in infants: comparison of intermittent uncooked cornstarch and continuous overnight glucose feedings.
Concept Glycogen Storage Disease
Concept Glycogen Storage Disease Type III
Concept Glycogen Storage Disease Type V
Concept Glycogen Storage Disease Type I
Concept Glycogen
Concept Glycogen Debranching Enzyme System
Concept Glycogen Storage Disease Type IV
Concept Glycogen Synthase
Academic Article Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics.
Academic Article Glycogen storage disease presenting as Cushing syndrome.
Search Criteria
  • Glycogen
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.