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Journal Abstract Search

258 related items for PubMed ID: 392211

  • 1. [Hereditary storage diseases of the liver (author's transl)].
    Schaub J.
    Leber Magen Darm; 1979 Sep; 9(5):227-34. PubMed ID: 392211
    [Abstract] [Full Text] [Related]

  • 2. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Sep; 42(12):61-71. PubMed ID: 7011274
    [Abstract] [Full Text] [Related]

  • 3. [Determination of blood level of muscle enzymes in glycogenoses with liver involvement: a diagnostic criterion].
    Labrune P, Chalas J, Pignon JP, Hennion C, Odièvre M.
    Ann Pediatr (Paris); 1989 May; 36(5):299-301. PubMed ID: 2742313
    [Abstract] [Full Text] [Related]

  • 4. [Genetic heterogeneity and the diagnosis of hepatic glycogenoses].
    Lemonnier A, Baussan C, Moatti N.
    C R Seances Soc Biol Fil; 1984 May; 178(4):327-47. PubMed ID: 6241011
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. [Metabolic disorders of the liver.Part 2: glycogen storage diseases, hereditary fructose intolerance, galactosemia and hepatic porphyrias].
    Donner MG, Erhardt A, Häussinger D.
    Dtsch Med Wochenschr; 2010 Dec; 135(50):2540-7. PubMed ID: 21140331
    [No Abstract] [Full Text] [Related]

  • 7. [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]

  • 8. [Hepatic glycogenosis: the clinical, biochemical and enzymatic aspects in a group of pediatric patients].
    Castro de Kolster C, Rolo M, Arias S, Guerreiro N, Carvajal A, Castro J, Kolster J.
    G E N; 1992 May 07; 46(3):191-8. PubMed ID: 1340824
    [Abstract] [Full Text] [Related]

  • 9. Inborn errors of carbohydrate metabolism.
    Mayatepek E, Hoffmann B, Meissner T.
    Best Pract Res Clin Gastroenterol; 2010 Oct 07; 24(5):607-18. PubMed ID: 20955963
    [Abstract] [Full Text] [Related]

  • 10. Glycogen storage diseases in Thai patients: Phramongkutklao Hospital experience.
    Kamolsilp M.
    J Med Assoc Thai; 2005 Nov 07; 88 Suppl 3():S295-301. PubMed ID: 16858972
    [Abstract] [Full Text] [Related]

  • 11. [Glycogenosis type VI. Report of two cases (author's transl)].
    D'Eufemia P, Cantani A, Corrado G, Gambarara M, Ruberto U, Giardini O.
    Pediatr Med Chir; 1981 Nov 07; 3(1):61-5. PubMed ID: 6795607
    [No Abstract] [Full Text] [Related]

  • 12. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
    Farmer PM.
    Ann Clin Lab Sci; 1982 Nov 07; 12(6):431-8. PubMed ID: 6817693
    [Abstract] [Full Text] [Related]

  • 13. [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 07; 18(10):3-8. PubMed ID: 4522459
    [No Abstract] [Full Text] [Related]

  • 14. [Glycogen storage disease].
    Kono N, Tarui S.
    Nihon Rinsho; 1990 Jul 07; 48(7):1504-9. PubMed ID: 2402067
    [No Abstract] [Full Text] [Related]

  • 15. [Diagnostic problems of hereditary intolerance to fructose in young infants].
    Odievre M.
    Arch Fr Pediatr; 1969 Jan 07; 26(1):5-19. PubMed ID: 5254366
    [No Abstract] [Full Text] [Related]

  • 16. [Tests for the detection of inborn errors of metabolism--urinary alpha-glucosidase analysis for the detection of glycogen storage disease type II (author's transl)].
    Soyama K, Ono E.
    Rinsho Byori; 1978 Dec 07; 26(12):1022-6. PubMed ID: 370427
    [No Abstract] [Full Text] [Related]

  • 17. Radiography of glycogen storage diseases.
    Miller JH, Stanley P, Gates GF.
    AJR Am J Roentgenol; 1979 Mar 07; 132(3):379-87. PubMed ID: 106640
    [Abstract] [Full Text] [Related]

  • 18. [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]

  • 19. [Histologic diagnosis of glucogenosis type IV (amylopectinosis) (author's transl)].
    Brass K.
    Z Kinderheilkd; 1974 Aug 15; 117(3):187-203. PubMed ID: 4528211
    [No Abstract] [Full Text] [Related]

  • 20. Glycogen-storage diseases of muscle: genetic problems.
    Rowland LP, DiMauro S.
    Res Publ Assoc Res Nerv Ment Dis; 1983 Aug 15; 60():239-54. PubMed ID: 6337394
    [No Abstract] [Full Text] [Related]

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