Lack of an alpha-1,4-glucan: alpha-... [Proc Natl Acad Sci U S A. 1966] - PubMed

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Type IV glycogenosis. Patient with absence of a branching enzyme alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyl transferase. [Lab Invest. 1968]
Type IV glycogenosis. Patient with absence of a branching enzyme alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyl transferase.
Reed GB Jr, Dixon JF, Neustein JB, Donnell GN, Landing BH. Lab Invest. 1968 Nov; 19(5):546-57.
Type IV glycogen-storage disease. Light-microscopic, electron-microscopic, and enzymatic study. [Am J Clin Pathol. 1976]
Type IV glycogen-storage disease. Light-microscopic, electron-microscopic, and enzymatic study.
Bannayan GA, Dean WJ, Howell RR. Am J Clin Pathol. 1976 Oct; 66(4):702-9.
Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes. [J Inherit Metab Dis. 1988]
Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes.
Shin YS, Steigüber H, Klemm P, Endres W, Schwab O, Wolff G. J Inherit Metab Dis. 1988; 11 Suppl 2:252-4.
Review Alpha-glucosidase administration: experiences in two patients with glycogen storage disease compared with animal experiments. [Birth Defects Orig Artic Ser. ...]
Review Alpha-glucosidase administration: experiences in two patients with glycogen storage disease compared with animal experiments.
Huijing F, Waltuck BL, Whelan WJ. Birth Defects Orig Artic Ser. 1973 Mar; 9(2):191-4.
Review [ENZYMATIC STUDY OF GLYCOGENOSIS]. [Ann Biol Clin (Paris). 1964]
Review [ENZYMATIC STUDY OF GLYCOGENOSIS].
HERS HG. Ann Biol Clin (Paris). 1964 Jan-Feb; 22:49-58.

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Cited by 13 PubMed Central articles

Living Donor Liver Transplantation in a Korean Child with Glycogen Storage Disease Type IV and a GBE1 Mutation. [Gut Liver. 2009]
Living Donor Liver Transplantation in a Korean Child with Glycogen Storage Disease Type IV and a GBE1 Mutation.
Ban HR, Kim KM, Jang JY, Kim GH, You HW, Kim K, Yu E, Kim DY, Kim KH, Lee YJ, et al. Gut Liver. 2009 Mar; 3(1):60-3. Epub 2009 Mar 31.
Crystal structure of full-length Mycobacterium tuberculosis H37Rv glycogen branching enzyme: insights of N-terminal beta-sandwich in substrate specificity and enzymatic activity. [J Biol Chem. 2010]
Crystal structure of full-length Mycobacterium tuberculosis H37Rv glycogen branching enzyme: insights of N-terminal beta-sandwich in substrate specificity and enzymatic activity.
Pal K, Kumar S, Sharma S, Garg SK, Alam MS, Xu HE, Agrawal P, Swaminathan K. J Biol Chem. 2010 Jul 2; 285(27):20897-903. Epub 2010 May 5.
A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats. [Mol Genet Metab. 2007]
A complex rearrangement in GBE1 causes both perinatal hypoglycemic collapse and late-juvenile-onset neuromuscular degeneration in glycogen storage disease type IV of Norwegian forest cats.
Fyfe JC, Kurzhals RL, Hawkins MG, Wang P, Yuhki N, Giger U, Van Winkle TJ, Haskins ME, Patterson DF, Henthorn PS. Mol Genet Metab. 2007 Apr; 90(4):383-92. Epub 2007 Jan 25.

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Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case o...
Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.
Proc Natl Acad Sci U S A. 1966 Aug ;56(2):725-9.

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Isovaleric acidemia: a new genetic defect of leucine metabolism.
Isovaleric acidemia: a new genetic defect of leucine metabolism.
Proc Natl Acad Sci U S A. 1966 Jul ;56(1):236-42.

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Hidden-figures-test performance: lasting effects of unilateral penetrating head injury and transient effects of bilateral cingulotomy.
Neuropsychologia. 1979 ;17(6):585-605.

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Osteosarcoma occurring in osteogenesis imperfecta. Report of two cases.
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The effect of plasma cholesterol lowering diet in male survivors of myocardial infarction. A controlled clinical trial.
Acta Med Scand Suppl. 1966 ;466:1-92.

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Lack of an alpha-1,4-glucan: alpha-1,4-glucan 6-glycosyl transferase in a case of type IV glycogenosis.

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