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Journal Abstract Search

148 related items for PubMed ID: 8438601

  • 1. [Glycogenoses and other metabolic hepatopathies in childhood and adolescence].
    Otting U, Hellmann C.
    Z Arztl Fortbild (Jena); 1993 Feb 12; 87(2):129-45. PubMed ID: 8438601
    [No Abstract] [Full Text] [Related]

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  • 3. [Curve of blood sugar and lactic acid in differential diagnosis of hepatic glycogenoses].
    Guminska M, Stopyrowa J, Szmigiel C, Halikowski B.
    Pol Tyg Lek; 1972 Feb 21; 27(8):290-3. PubMed ID: 4501499
    [No Abstract] [Full Text] [Related]

  • 4. [Biochemical diagnosis of different types of liver glycogenosis].
    Chibisov IV, Chistova LV, Pinzur ED, Leont'ev AF, Popova IA.
    Vopr Okhr Materin Det; 1973 Oct 21; 18(10):3-8. PubMed ID: 4522459
    [No Abstract] [Full Text] [Related]

  • 5. [Method for the differentiation of glycogenoses].
    Schaub J.
    Monatsschr Kinderheilkd (1902); 1970 Jun 21; 118(6):427-9. PubMed ID: 4331992
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  • 6. [Glycogenoses--genetic disorders leading to disturbed glycogen metabolism].
    Bejtka M, Malińska D.
    Postepy Biochem; 2011 Jun 21; 57(2):148-57. PubMed ID: 21913415
    [Abstract] [Full Text] [Related]

  • 7. [Difficulties in determination of the type of glycogenosis].
    Minculescu M, Onofrei T, Rusu M, Septilici N, Minculescu I, Popa V, Serbănescu C, Pena J, Wolcz G, Ionuş D, Galaczi A.
    Pediatria (Bucur); 1974 Jan 21; 23(1):19-34. PubMed ID: 4526155
    [No Abstract] [Full Text] [Related]

  • 8. Glycogen storage disease. (Report of three cases).
    Devi T, Mathew O.
    Indian Pediatr; 1971 Jan 21; 8(1):43-5. PubMed ID: 5284580
    [No Abstract] [Full Text] [Related]

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  • 10. [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 15; 91(10):667-9. PubMed ID: 9019646
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  • 13. [Hepatic glycogenosis; enzyme study].
    Gilly R, Reynier M, Ricci R, Vernon L, Chamfeuil R, Marty J.
    Mars Med; 1970 Jun 15; 107(6):451-6. PubMed ID: 5269978
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  • 15. 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 15; 140(6):781-3. PubMed ID: 12072888
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  • 16. Genetic studies in glycogen storage disease type 3.
    Waaler E, Garatun-Tjeldsto O, Moe PJ.
    Acta Paediatr Scand; 1970 Sep 15; 59(5):529-35. PubMed ID: 5272597
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  • 17. [Diagnostic problems in various types of glycogenosis].
    Tulzer W, Ploier R, Klatt R.
    Wien Med Wochenschr; 1974 Jun 22; 124(25):428-31. PubMed ID: 4525974
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  • 19. Hepatic storage of glycogen in Niemann-Pick disease type B.
    Smith WE, Kahler SG, Frush DP, Milov DE, Gottfried MR, Chen YT.
    J Pediatr; 2001 Jun 22; 138(6):946-8. PubMed ID: 11391349
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