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5. [Glycogen storage disease in adult brothers--with special reference to association of gout]. Hirao N; Nobunaga M; Shimazu Y; Kawamura T; Fukuda M Ryumachi; 1972 Nov; 12(3):214-25. PubMed ID: 4514491 [No Abstract] [Full Text] [Related]
6. [Continuous nocturnal intragastric feeding in glycogenosis type I and III]. de Parscau L; Guibaud P; Hermier M; François R Pediatrie; 1986; 41(3):197-203. PubMed ID: 3095784 [TBL] [Abstract][Full Text] [Related]
7. Studies in glycogen storage disease. II. Heterogeneity in the inheritance of glycogen storage diseases. Field JB; Drash AL Trans Assoc Am Physicians; 1967; 80():284-96. PubMed ID: 4295468 [No Abstract] [Full Text] [Related]
8. [Liver glycogenosis: first 2 Brazilian cases with double enzyme defect]. Seibt FL; Mello de Oliveira JA; Santoro JR; Alcantara A; Dora GL; Pena GA Ann Histochim; 1973; 18(3):253-65. PubMed ID: 4526225 [No Abstract] [Full Text] [Related]
14. [Hepatic forms of glycogenosis - clinical and biochemical findings in 15 cases]. Pronicka E; Pieniazek D; Miłoszewska E; Gruszczyńska B; Moszczyńska A Pediatr Pol; 1983 May; 58(5):437-45. PubMed ID: 6579490 [No Abstract] [Full Text] [Related]
15. Heterogenous glycogen storage disease in one family. Domaniç N; Akman N; Ozand P; Müftüoglu AU Hum Hered; 1976; 26(3):217-25. PubMed ID: 1066318 [TBL] [Abstract][Full Text] [Related]
16. Glycogen storage diseases: a review with emphasis on gastrointestinal manifestations. Sidbury JB; Heick HM South Med J; 1968 Sep; 61(9):915-22. PubMed ID: 4877692 [No Abstract] [Full Text] [Related]
17. Glycogen-storage diseases of muscle: genetic problems. Rowland LP; DiMauro S Res Publ Assoc Res Nerv Ment Dis; 1983; 60():239-54. PubMed ID: 6337394 [No Abstract] [Full Text] [Related]
18. [Genetic heterogeneity and the diagnosis of hepatic glycogenoses]. Lemonnier A; Baussan C; Moatti N C R Seances Soc Biol Fil; 1984; 178(4):327-47. PubMed ID: 6241011 [TBL] [Abstract][Full Text] [Related]
19. Glycogen synthase deficiency (glycogen storage disease type 0) presenting with hyperglycemia and glucosuria: report of three new mutations. Bachrach BE; Weinstein DA; Orho-Melander M; Burgess A; Wolfsdorf JI J Pediatr; 2002 Jun; 140(6):781-3. PubMed ID: 12072888 [TBL] [Abstract][Full Text] [Related]
20. [Glycogenosis with cirrhosis in 2 brothers. Significance of the demonstrated enzyme defects]. Gentil C; Odievre M; Vassoyan J; Alagille D Arch Fr Pediatr; 1972 Jan; 29(1):79-97. PubMed ID: 4504126 [No Abstract] [Full Text] [Related] [Next] [New Search]