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PUBMED FOR HANDHELDS

Journal Abstract Search

137 related items for PubMed ID: 6772352

  • 41.
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  • 42.
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  • 43. Genetic heterogeneity of membrane-bound beta-glucosidase in Gaucher's disease.
    Carroll M.
    J Inherit Metab Dis; 1981; 4(1):11-3. PubMed ID: 6785517
    [Abstract] [Full Text] [Related]

  • 44. Leukocyte beta-glucosidase in homozygotes and heterozygotes for Gaucher disease.
    Raghavan SS, Topol J, Kolodny EH.
    Am J Hum Genet; 1980 Mar; 32(2):158-73. PubMed ID: 6770675
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  • 45.
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  • 47. Soluble and membranous neutral beta-glucosidases.
    Ben-Yoseph Y, Nadler HL.
    Prog Clin Biol Res; 1982 Mar; 95():465-80. PubMed ID: 6812082
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  • 49. 4-Methylumbelliferyl-beta-glucosidase in cultured human fibroblasts from controls and patients with Gaucher's disease.
    Hultberg B, Sjöblad S, Ockerman PA.
    Clin Chim Acta; 1973 Nov 23; 49(1):93-7. PubMed ID: 4764343
    [No Abstract] [Full Text] [Related]

  • 50. Multiple forms of human skin fibroblast beta-glucosidase and their activation by fibroblast monosialoglycosphingolipids.
    Saito M, Mueller OT, Rosenberg A.
    Prog Clin Biol Res; 1982 Nov 23; 95():385-403. PubMed ID: 6812078
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  • 51. Prenatal diagnosis of Gaucher disease. Assay of the beta-glucosidase activity in amniotic fluid cells cultivated in two laboratories with different cultivation conditions.
    Svennerholm L, Håkansson G, Lindsten J, Wahlström J, Dreborg S.
    Clin Genet; 1981 Jan 23; 19(1):16-22. PubMed ID: 6780254
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  • 52. [Gaucher's disease (type 1) with clinical picture like a myelodysplastic syndrome: the difference between this Gaucher's cell and CML pseudo-Gaucher's cell].
    Saito H, Uemura K, Maruyama T, Kawakami H, Iijima Y, Kitano K, Kaji R, Furuta S.
    Rinsho Ketsueki; 1987 Aug 23; 28(8):1449-55. PubMed ID: 3123742
    [No Abstract] [Full Text] [Related]

  • 53. Effectors of three beta-glucosidases from human liver.
    Daniels LB, Gnarra JR, Glew RH.
    Prog Clin Biol Res; 1982 Aug 23; 95():333-55. PubMed ID: 6812077
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  • 54. Gaucher disease: accurate identification of asymptomatic French-Canadian carrier using nonlabeled authentic sphingolipid substrate N-palmitoyl dihydroglucocerebroside.
    Choy FY, Bouillon L, Laurin CA.
    Am J Med Genet; 1987 Aug 23; 27(4):895-905. PubMed ID: 3425599
    [Abstract] [Full Text] [Related]

  • 55. Genetic heterogeneity in type I Gaucher disease.
    Devine EA, Beighton P, Petersen EM, Desnick RJ.
    Prog Clin Biol Res; 1982 Aug 23; 95():495-510. PubMed ID: 6812084
    [Abstract] [Full Text] [Related]

  • 56. Studies on human acid beta-glucosidase and the nature of the molecular defect in type 1 Ashkenazi Gaucher disease.
    Gatt S, Dinur T, Desnick RJ.
    Prog Clin Biol Res; 1982 Aug 23; 95():315-31. PubMed ID: 6812076
    [No Abstract] [Full Text] [Related]

  • 57. Enzymic differentiation of neurologic and nonneurologic forms of Gaucher's disease.
    Glew RH, Daniels LB, Clark LS, Hoyer SW.
    J Neuropathol Exp Neurol; 1982 Nov 23; 41(6):630-41. PubMed ID: 6813430
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  • 58. Infantile Gaucher's disease: glucocerebrosidase deficiency in peripheral blood leukocytes and cultured fibroblasts.
    Sengers RC, Lamers KJ, Bakkeren JA, Schretlen ED, Trijbels JM.
    Neuropadiatrie; 1975 Nov 23; 6(4):377-82. PubMed ID: 241947
    [Abstract] [Full Text] [Related]

  • 59. Gaucher's disease in the Cape coloured population of the RSA, including a family with 5 affected siblings.
    Swart AL, Hesseling PB, Hayden MR, Louw M, Herbert JS.
    S Afr Med J; 1987 Jan 24; 71(2):97-9. PubMed ID: 3101207
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  • 60. The diagnosis of Gaucher's disease in liver using 4-methylumbelliferyl-beta-D-glucopyranoside.
    Broadhead DM, Butterworth J.
    Clin Chim Acta; 1977 Feb 15; 75(1):155-61. PubMed ID: 14796
    [Abstract] [Full Text] [Related]

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