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Journal Abstract Search

233 related items for PubMed ID: 7573152

  • 41. [Biochemical study of cerebral and hepatic lipids in a case of Tay-Sachs disease].
    Grégoire PE, Jonniaux G, Loeb H, Voet W, Capelle R.
    Rev Fr Etud Clin Biol; 1969; 14(6):568-74. PubMed ID: 5824260
    [No Abstract] [Full Text] [Related]

  • 42. [Sialic acid in breast milk and infant formula food].
    Heine W, Wutzke KD, Radke M.
    Monatsschr Kinderheilkd; 1993 Dec; 141(12):946-50. PubMed ID: 8114778
    [Abstract] [Full Text] [Related]

  • 43. Storage of gangliosides GM2 and fucosyl GM1 in the kidney of MCC strain of mastomys (Praomys coucha).
    Takimoto K, Kawamura N, Kasama T.
    J Biochem; 2009 Sep; 146(3):439-47. PubMed ID: 19556222
    [Abstract] [Full Text] [Related]

  • 44. [Lysosomal glycosidases and glycoproteinoses].
    Montreuil J.
    C R Seances Soc Biol Fil; 1981 Sep; 175(5):694-707. PubMed ID: 6456795
    [Abstract] [Full Text] [Related]

  • 45. Relationship between gamma-glutamyl transpeptidase activity and sialic acid content in some organs and brain regions of the developing rat.
    Dvoráková L, Stastný F, Lisý V.
    Biochem Mol Biol Int; 1994 Dec; 34(6):1137-45. PubMed ID: 7696986
    [Abstract] [Full Text] [Related]

  • 46. Lysosomal biogenesis in lysosomal storage disorders.
    Karageorgos LE, Isaac EL, Brooks DA, Ravenscroft EM, Davey R, Hopwood JJ, Meikle PJ.
    Exp Cell Res; 1997 Jul 10; 234(1):85-97. PubMed ID: 9223373
    [Abstract] [Full Text] [Related]

  • 47. Prenatal diagnosis and confirmation of infantile sialic acid storage disease.
    Vamos E, Libert J, Elkhazen N, Jauniaux E, Hustin J, Wilkin P, Baumkötter J, Mendla K, Cantz M, Strecker G.
    Prenat Diagn; 1986 Jul 10; 6(6):437-46. PubMed ID: 3809113
    [Abstract] [Full Text] [Related]

  • 48. Hydrops fetalis: lysosomal storage disorders in extremis.
    Stone DL, Sidransky E.
    Adv Pediatr; 1999 Jul 10; 46():409-40. PubMed ID: 10645471
    [Abstract] [Full Text] [Related]

  • 49. [Sialic acids (brief review of the results obtained in 25 years)].
    Cabezas JA.
    Rev Esp Fisiol; 1982 Jul 10; 38 Suppl():29-35. PubMed ID: 7146586
    [Abstract] [Full Text] [Related]

  • 50. Prenatal diagnosis of infantile sialic acid storage disease in a twin pregnancy.
    Lake BD, Young EP, Nicolaides K.
    J Inherit Metab Dis; 1989 Jul 10; 12(2):152-6. PubMed ID: 2502674
    [Abstract] [Full Text] [Related]

  • 51. Clinical, morphological, and molecular aspects of sialic acid storage disease manifesting in utero.
    Froissart R, Cheillan D, Bouvier R, Tourret S, Bonnet V, Piraud M, Maire I.
    J Med Genet; 2005 Nov 10; 42(11):829-36. PubMed ID: 15805149
    [Abstract] [Full Text] [Related]

  • 52. [Glycoproteins and glycoproteinosis].
    Strecker G, Montreuil J.
    Biochimie; 1979 Nov 10; 61(11-12):1199-246. PubMed ID: 120204
    [No Abstract] [Full Text] [Related]

  • 53. Free sialic acid storage disease. A new Italian case.
    Fois A, Balestri P, Farnetani MA, Mancini GM, Borgogni P, Margollicci MA, Molinelli M, Alessandrini C, Gerli R.
    Eur J Pediatr; 1987 Mar 10; 146(2):195-8. PubMed ID: 3569361
    [Abstract] [Full Text] [Related]

  • 54. The effect of D-(+)-glucosamine on levels of free N-acetylneuraminic acid and UDP-N-acetylhexosamines in infantile sialic acid storage disease (ISSD) fibroblasts.
    Paschke E, Höfler G, Roscher A.
    J Inherit Metab Dis; 1987 Mar 10; 10(1):48-51. PubMed ID: 3106716
    [Abstract] [Full Text] [Related]

  • 55. Functional characterization of wild-type and mutant human sialin.
    Morin P, Sagné C, Gasnier B.
    EMBO J; 2004 Nov 24; 23(23):4560-70. PubMed ID: 15510212
    [Abstract] [Full Text] [Related]

  • 56.
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  • 57. Biochemical characterization of patients and prenatal diagnosis of sialic acid storage disease for three families.
    Clements PR, Taylor JA, Hopwood JJ.
    J Inherit Metab Dis; 1988 Nov 24; 11(1):30-44. PubMed ID: 3128687
    [Abstract] [Full Text] [Related]

  • 58. [Contribution of electron microscopy of cultures of fibroblasts in the diagnosis of hereditary metabolic diseases].
    Jaffray JY, Charbonne F, Rousseau P, Malpuech G, Meyer M, Labbe A, Malet P.
    Pathol Biol (Paris); 1986 Feb 24; 34(2):91-8. PubMed ID: 3517782
    [Abstract] [Full Text] [Related]

  • 59. A novel mutation in the SLC17A5 gene causing both severe and mild phenotypes of free sialic acid storage disease in one inbred Bedouin kindred.
    Landau D, Cohen D, Shalev H, Pinsk V, Yerushalmi B, Zeigler M, Birk OS.
    Mol Genet Metab; 2004 Jun 24; 82(2):167-72. PubMed ID: 15172005
    [Abstract] [Full Text] [Related]

  • 60.
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