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Journal Abstract Search

207 related items for PubMed ID: 182428

  • 1. The glycogenoses and other inherited disorders of carbohydrate metabolism.
    Senior B, Sadeghi-Nejad A.
    Clin Perinatol; 1976 Mar; 3(1):79-98. PubMed ID: 182428
    [No Abstract] [Full Text] [Related]

  • 2. Disorders of carbohydrate metabolism.
    Howanitz PJ, Howanitz JH.
    Clin Lab Med; 1981 Jun; 1(2):419-32. PubMed ID: 7049524
    [No Abstract] [Full Text] [Related]

  • 3. [Congenital enzyme deficiency in carbohydrate metabolism. Its significance for clinical pediatrics and human biochemical genetics (author's transl)].
    Schaub J, Osang M.
    MMW Munch Med Wochenschr; 1976 May 07; 118(19):609-14. PubMed ID: 180406
    [Abstract] [Full Text] [Related]

  • 4. [Coexistence of liver glycogenosis, Fanconi's syndrome and abnormal galactose metabolism in a 3-year-old child].
    Klinowska W, Iwańczak F, Jagodzińska M.
    Pol Tyg Lek; 1980 Dec 29; 35(52):2065-6. PubMed ID: 6945566
    [No Abstract] [Full Text] [Related]

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  • 7. [Current problems in liver and bile duct diseases in childhood. 2].
    Gudowski G, Tambor U, Laske G.
    Z Arztl Fortbild (Jena); 1976 Aug 15; 70(15):825-30. PubMed ID: 1068600
    [No Abstract] [Full Text] [Related]

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  • 9. [Enzyme-diseases in childhood].
    Berger H.
    Wien Med Wochenschr; 1976 Sep 03; 126(36):501-4. PubMed ID: 1069410
    [No Abstract] [Full Text] [Related]

  • 10. [Enzymatic analysis for the diagnosis of inborn errors of carbohydrate metabolism].
    Kusunoki T, Soyama K, Oya N, Kinugasa A.
    Nihon Rinsho; 1979 Jun 29; Suppl():1619-23. PubMed ID: 290838
    [No Abstract] [Full Text] [Related]

  • 11. [Screening of newborns for inborn errors of galactose metabolism. Methods and results].
    Gitzelmann R.
    Monatsschr Kinderheilkd (1902); 1976 Sep 29; 129(9):654-7. PubMed ID: 185513
    [Abstract] [Full Text] [Related]

  • 12. Hexose and protein tolerance tests in children with liver glycogenosis caused by a deficiency of the debranching enzyme system.
    Fernandes J, van de Kamer JH.
    Pediatrics; 1968 May 29; 41(5):935-44. PubMed ID: 5240685
    [No Abstract] [Full Text] [Related]

  • 13. On the screening for inborn errors of galactose metabolism.
    Vaca G, Sànchez-Corona J, Olivares N, Medina C, Ibarra B, Cantú JM.
    Ann Genet; 1983 May 29; 26(3):191-2. PubMed ID: 6606384
    [Abstract] [Full Text] [Related]

  • 14. Inborn errors of carbohydrate metabolism.
    Mayatepek E, Hoffmann B, Meissner T.
    Best Pract Res Clin Gastroenterol; 2010 Oct 29; 24(5):607-18. PubMed ID: 20955963
    [Abstract] [Full Text] [Related]

  • 15. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.
    Iwamasa T, Ninomiya N, Fukuda S, Hamada T, Hirashima M, Osame M.
    Pathol Res Pract; 1983 Mar 29; 176(2-4):236-52. PubMed ID: 6304667
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  • 16. High liver glycogen in hereditary fructose intolerance.
    Cain AR, Ryman BE.
    Gut; 1971 Nov 29; 12(11):929-32. PubMed ID: 5289293
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  • 17. [Hereditary fructose intolerance].
    Vaisman N, Cooper M, Garti R.
    Harefuah; 1981 May 15; 100(10):464-6. PubMed ID: 7308886
    [No Abstract] [Full Text] [Related]

  • 18. [Differential diagnosis between hereditary fructose intolerance and fructose-1,6-diphosphatase deficiency].
    Méndez Aparicio FM.
    Rev Clin Esp; 1981 May 15; 161(5-6):289-96. PubMed ID: 6270745
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  • 20. Hepatic glycogen storage disease. Clinical and laboratory findings in 23 cases.
    Spencer-Peet J, Norman ME, Lake BD, McNamara J, Patrick AD.
    Q J Med; 1971 Jan 15; 40(157):95-114. PubMed ID: 5282941
    [No Abstract] [Full Text] [Related]

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