Generalized glycogenosis: Report of a case with deficiency of alpha glucosidase
- 31 August 1964
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 65 (2), 243-251
- https://doi.org/10.1016/s0022-3476(64)80526-6
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Diagnosis of generalized glycogen storage disease (Pompe's disease)The Journal of Pediatrics, 1963
- Amylo-1,6-glucosidase activity in leucocytes from patients with glycogen storage diseaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1963
- LEUKOCYTE DEBRANCHING ENZYME IN GLYCOGEN STORAGE DISEASEJournal of Clinical Investigation, 1963
- An improved micromethod for the determination of glucose-6-phosphatase activityClinica Chimica Acta; International Journal of Clinical Chemistry, 1963
- LOW LEUKOCYTE PHOSPHORYLASE IN HEPATIC PHOSPHORYLASE-DEFICIENT GLYCOGEN STORAGE DISEASEJournal of Clinical Investigation, 1961
- PHOSPHORYLASE ACTIVITY IN LEUCOCYTES FROM PATIENTS WITH GLYCOGEN-STORAGE DISEASEThe Lancet, 1961
- A glucose oxidase reagent for maltase assayAnalytical Biochemistry, 1961
- Degradation of glycogen in tissues from generalized glycogen storage diseaseBiochimica et Biophysica Acta, 1961
- CHRONIC PROGRESSIVE MYOPATHY WITH MYOGLOBINURIA: DEMONSTRATION OF A GLYCOGENOLYTIC DEFECT IN THE MUSCLE*Journal of Clinical Investigation, 1959
- A RELATION BETWEEN NON-ESTERIFIED FATTY ACIDS IN PLASMA AND THE METABOLISM OF GLUCOSEJournal of Clinical Investigation, 1956