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10. Lysosomal alpha-glucosidase in type II glycogenosis; activity in leukocytes and cell cultures in relation to genotype. Nitowsky HM; Grunfeld A J Lab Clin Med; 1967 Mar; 69(3):472-84. PubMed ID: 5226931 [No Abstract] [Full Text] [Related]
15. [Detection of heterozygote carriers of liver variant of glycogenosis]. Chibisov IV Vopr Med Khim; 1982; 28(3):46-7. PubMed ID: 6954760 [No Abstract] [Full Text] [Related]
16. A new mutation in PRKAG2 gene causing hypertrophic cardiomyopathy with conduction system disease and muscular glycogenosis. Laforêt P; Richard P; Said MA; Romero NB; Lacene E; Leroy JP; Baussan C; Hogrel JY; Lavergne T; Wahbi K; Hainque B; Duboc D Neuromuscul Disord; 2006 Mar; 16(3):178-82. PubMed ID: 16487706 [TBL] [Abstract][Full Text] [Related]
17. [Histochemical study on skin culture in type II glycogenosis]. Tenconi R; Baccichetti C Riv Anat Patol Oncol; 1968; 33():520-3. PubMed ID: 5280244 [No Abstract] [Full Text] [Related]
18. Report of the first family of glycogen storage disease among Egyptians. el Gholmy A; Hashem N; Khalifa AS; Osman N; Abdel Hamid G J Egypt Med Assoc; 1965; 48(2):130-41. PubMed ID: 5213078 [No Abstract] [Full Text] [Related]
19. [Different phenotypes of type IXb glycogenosis (phosphorylase-b-kinase deficiency) in adult- and early childhood]. Müller P; Bührdel P; Freidt B; Böhme HJ Med Klin (Munich); 1996 Oct; 91(10):667-9. PubMed ID: 9019646 [No Abstract] [Full Text] [Related]
20. Families with X-linked liver glycogenosis due to phosphorylase kinase deficiency. Willems P Clin Genet; 1990 Jul; 38(1):80. PubMed ID: 2387090 [No Abstract] [Full Text] [Related] [Next] [New Search]