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Journal Abstract Search

134 related items for PubMed ID: 116085

  • 21.
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  • 22.
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  • 23. Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria.
    Mononen I, Kaartinen V, Mononen T.
    J Inherit Metab Dis; 1988; 11(2):194-8. PubMed ID: 3139932
    [Abstract] [Full Text] [Related]

  • 24. Letter: Aspartylglycosaminuria in Northern Norway.
    Borud O, Torp KH.
    Lancet; 1976 May 15; 1(7968):1082-3. PubMed ID: 57494
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  • 25.
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  • 26. Homozygous NADH-methemoglobin reductase and aspartylglucosaminidase deficiencies in a moderately retarded Sicilian child.
    Musumeci S, Salvati A, Schiliró G, Salvo G, Di Dio R, Caprari P.
    Am J Med Genet; 1984 Dec 15; 19(4):643-50. PubMed ID: 6517093
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  • 28. Enzymatic determination of urinary aspartylglycosylamine: a rapid and sensitive-method to detect aspartylclycosylaminuria (AGU).
    Sugahara K, Nishimura K, Aula P, Yamashina IY.
    Clin Chim Acta; 1976 Oct 15; 72(2):265-7. PubMed ID: 987869
    [No Abstract] [Full Text] [Related]

  • 29. [Skeletal changes in 2 German children with aspartylglycosaminuria].
    Schmidt H, Ziegler R, Ullrich K, von Lengerke JH, Sewell AC.
    Rofo; 1988 Aug 15; 149(2):143-6. PubMed ID: 2842830
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  • 30.
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  • 31. Follow-up in patients with aspartylglucosaminuria. Part I. The course of intellectual functions.
    Arvio M.
    Acta Paediatr; 1993 May 15; 82(5):469-71. PubMed ID: 8518524
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  • 32.
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  • 33. Regional distribution of glycoasparagine storage material in the brain in aspartylglycosaminuria.
    Maury CP, Haltia M, Palo J.
    J Neurol Sci; 1981 May 15; 50(2):291-8. PubMed ID: 6164750
    [Abstract] [Full Text] [Related]

  • 34. Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patients.
    Autio S, Visakorpi JK, Järvinen H.
    Ann Clin Res; 1973 Jun 15; 5(3):149-55. PubMed ID: 4356121
    [No Abstract] [Full Text] [Related]

  • 35. Aspartylglucosaminuria in a Canadian family.
    Gordon BA, Rupar CA, Rip JW, Haust MD, Coulter-Mackie MB, Scott E, Hinton GG.
    Clin Invest Med; 1998 Jun 15; 21(3):114-23. PubMed ID: 9627765
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  • 36. Aspartylglycosaminuria diagnosed by routine urine amino acid assay.
    Rudy JL.
    Clin Chem; 1988 Oct 15; 34(10):2164. PubMed ID: 3168251
    [No Abstract] [Full Text] [Related]

  • 37. Gingival biopsy in diagnosis of inborn storage diseases: a case of aspartylglycosaminuria.
    Bonnaure-Mallet M, Loiseau-Corvez MN, Goasguen J, Apiou J, Jezequel C.
    J Oral Pathol Med; 1991 May 15; 20(5):237-40. PubMed ID: 2066874
    [Abstract] [Full Text] [Related]

  • 38. The genetic mucolipidoses--definition and classification.
    Spranger J.
    Birth Defects Orig Artic Ser; 1975 May 15; 11(6):251-6. PubMed ID: 811278
    [No Abstract] [Full Text] [Related]

  • 39. Analysis of aspartylglucosamine at the picomole level by high-performance liquid chromatography.
    Kaartinen V, Mononen I.
    J Chromatogr; 1989 May 30; 490(2):293-9. PubMed ID: 2768403
    [Abstract] [Full Text] [Related]

  • 40. Aspartylglucosaminuria in the United States.
    Hreidarsson S, Thomas GH, Valle DL, Stevenson RE, Taylor H, McCarty J, Coker SB, Green WR.
    Clin Genet; 1983 Jun 30; 23(6):427-35. PubMed ID: 6883788
    [Abstract] [Full Text] [Related]

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