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3. [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]
5. Diet and growth of children with glycogen storage disease Types I and III. Daeschel IE; Janick LS; Kramish MJ; Coleman RA J Am Diet Assoc; 1983 Aug; 83(2):135-41. PubMed ID: 6409953 [TBL] [Abstract][Full Text] [Related]
8. [Carbohydrates in the treatment of glycogenoses]. Hayde M; Widhalm K Infusionstherapie; 1990 Apr; 17(2):69-72. PubMed ID: 2113038 [TBL] [Abstract][Full Text] [Related]
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10. [Type I glycogenosis: extending therapy with uncooked cornstarch]. Biggemann B; Hilgarth R; Wendel U Monatsschr Kinderheilkd; 1986 Mar; 134(3):142-5. PubMed ID: 3084952 [TBL] [Abstract][Full Text] [Related]
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12. Molecular prenatal diagnosis of glycogen storage disease type Ia. Qu Y; Abdenur JE; Eng CM; Desnick RJ Prenat Diagn; 1996 Apr; 16(4):333-6. PubMed ID: 8734807 [TBL] [Abstract][Full Text] [Related]
13. Gastric drip feeding in patients with glycogen storage disease type I: its effects on growth and plasma lipids and apolipoproteins. Fernandes J; Alaupovic P; Wit JM Pediatr Res; 1989 Apr; 25(4):327-31. PubMed ID: 2542871 [TBL] [Abstract][Full Text] [Related]
14. Review of the glycogen storage diseases. Bitar J J Med Liban; 1986; 36(2):72-5. PubMed ID: 3537297 [No Abstract] [Full Text] [Related]
15. Glycogen storage disease type I and III and pyruvate carboxylase deficiency: results of long-term treatment with uncooked cornstarch. Ullrich K; Schmidt H; van Teeffelen-Heithoff A Acta Paediatr Scand; 1988 Jul; 77(4):531-6. PubMed ID: 3134793 [TBL] [Abstract][Full Text] [Related]
16. The behavior of hepatic phosphorylase b kinase, phosphorylase a and b after administration of glucagon to patients with glycogen storage disease type VIa. Pieniazek D; Pronicka E; Pawłowska J Horm Metab Res; 1986 Aug; 18(8):546-50. PubMed ID: 3093350 [TBL] [Abstract][Full Text] [Related]
17. [Prenatal diagnosis of glycogen storage disease Ia by screening for hot spot mutations in combination with the 1176 nucleotide polymorphism linkage analysis]. Qiu WJ; Zhang YF; Pan J; Ye J; Liu XQ; Han LS; Gu XF Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Feb; 22(1):44-8. PubMed ID: 15696478 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of glycogen storage disease type 1a by direct mutation detection. Wong LJ Prenat Diagn; 1996 Feb; 16(2):105-8. PubMed ID: 8650119 [TBL] [Abstract][Full Text] [Related]
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20. Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomes. Kido J; Nakamura K; Matsumoto S; Mitsubuchi H; Ohura T; Shigematsu Y; Yorifuji T; Kasahara M; Horikawa R; Endo F J Hum Genet; 2013 May; 58(5):285-92. PubMed ID: 23486339 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]