These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
129 related articles for article (PubMed ID: 4522834)
1. Urinary excretion of C6-C10 dicarboxylic acids in glycogen storage disease types I and 3. Dosman J; Crawhall JC; Klassen GA; Mamer OA; Neumann P Clin Chim Acta; 1974 Feb; 51(1):93-101. PubMed ID: 4522834 [No Abstract] [Full Text] [Related]
2. Hyperuricemia and dicarboxylicaciduria in glycogen storage disease. Dosman JA; Crawhill JC; Klassen GA; Mamer OA Adv Exp Med Biol; 1973; 41():361-6. PubMed ID: 4524742 [No Abstract] [Full Text] [Related]
3. Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease. Mize CE; Waber LJ; Anderson T; Bennett MJ J Inherit Metab Dis; 1997 Jul; 20(3):407-10. PubMed ID: 9266368 [No Abstract] [Full Text] [Related]
4. Dicarboxylic aciduria during ketotic phases in various types of glycogen storage disease. Pettersen JE; Winsnes A Acta Paediatr Scand; 1981; 70(3):309-13. PubMed ID: 6941627 [TBL] [Abstract][Full Text] [Related]
5. [Metabolism studies in children and young adults with glycogenoses]. Matschke I; Neubaur J; Willms B; Wolf H Monatsschr Kinderheilkd (1902); 1969 Apr; 117(4):259-62. PubMed ID: 5270571 [No Abstract] [Full Text] [Related]
6. Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease). Hallgren P; Hansson G; Henriksson KG; Häger A; Lundblad A; Svensson S Eur J Clin Invest; 1974 Dec; 4(6):429-33. PubMed ID: 4531383 [No Abstract] [Full Text] [Related]
8. Sedimentation characteristics of native glycogens from human glycogen-storage diseases. Bueding E; Sidbury J; Orrell SA Biochem Med; 1970 Apr; 3(5):355-64. PubMed ID: 5289042 [No Abstract] [Full Text] [Related]
9. An unusual case of glycogen storage disease. Moses SW Adv Exp Med Biol; 1973; 41():353-9. PubMed ID: 4364689 [No Abstract] [Full Text] [Related]
10. Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency. Bergoffen J; Kaplan P; Hale DE; Bennett MJ; Berry GT J Inherit Metab Dis; 1993; 16(5):851-6. PubMed ID: 8295400 [TBL] [Abstract][Full Text] [Related]
11. Metabolic studies in liver glycogen disease with special reference to lactate metabolism. Zuppinger K; Rossi E Helv Med Acta; 1970 Dec; 35(5):406-22. PubMed ID: 5278209 [No Abstract] [Full Text] [Related]
12. [Biochemical diagnosis of different types of liver glycogenosis]. Chibisov IV; Chistova LV; Pinzur ED; Leont'ev AF; Popova IA Vopr Okhr Materin Det; 1973 Oct; 18(10):3-8. PubMed ID: 4522459 [No Abstract] [Full Text] [Related]
13. The dietary management of hepatic glycogen storage disease. Leonard JV; Francis DE; Dunger DB Proc Nutr Soc; 1979 Dec; 38(3):321-4. PubMed ID: 294590 [No Abstract] [Full Text] [Related]
14. Hyperlipemia in children with liver glycogen disease. Fernandes J; Pikaar NA Am J Clin Nutr; 1969 May; 22(5):617-27. PubMed ID: 5254184 [No Abstract] [Full Text] [Related]
15. Studies of factors affecting gluconeogenesis and glycolysis in glycogenoses of the liver. Sadeghi-Nejad A; Loridan L; Senior B J Pediatr; 1970 Apr; 76(4):561-70. PubMed ID: 4316065 [No Abstract] [Full Text] [Related]
16. Studies of liver glycogenoses, with particular reference to the metabolism of intravenously administered glycerol. Senior B; Loridan L N Engl J Med; 1968 Oct; 279(18):958-65. PubMed ID: 4300572 [No Abstract] [Full Text] [Related]
17. [A case of "debrancher" glycogenosis]. Ikeda H; Murase T; Nakao K Nihon Naika Gakkai Zasshi; 1971 Aug; 60(8):748-55. PubMed ID: 4255094 [No Abstract] [Full Text] [Related]
18. GLYCOGEN STORAGE DISEASE. BIOCHEMICAL AND CLINICAL DATA IN SIXTEEN CASES. VAN CREVELD ; HUIJING F Am J Med; 1965 Apr; 38():554-61. PubMed ID: 14271742 [No Abstract] [Full Text] [Related]