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Journal Abstract Search

198 related items for PubMed ID: 16933855

  • 1. [The possibility of increasing the precision of biochemical diagnostics of Gaucher disease].
    Horovenko NH, Drozdova VD, Nedoboĭ AM, Ol'khovych NV, Pichkur NO, Tsyhankova MA, Radzikhovs'ka OV.
    Tsitol Genet; 2006; 40(3):67-71. PubMed ID: 16933855
    [Abstract] [Full Text] [Related]

  • 2. [The biochemical diagnosis of Gaucher disease].
    Yargui L, Mokhtari S, Arab M, Berhoune A.
    Arch Pediatr; 2005 Aug; 12(8):1301-9. PubMed ID: 15878824
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  • 3. Biochemical study on beta-glucosidase in individuals with Gaucher's disease and normal subjects.
    Michelin K, Wajner A, Goulart Lda S, Fachel AA, Pereira ML, de Mello AS, Souza FT, Pires RF, Giugliani R, Coelho JC.
    Clin Chim Acta; 2004 May; 343(1-2):145-53. PubMed ID: 15115687
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  • 4. Phenotypic manifestations of Gaucher disease: clinical features in 48 biochemically verified type 1 patients and comment on type 2 patients.
    Kolodny EH, Ullman MD, Mankin HJ, Raghavan SS, Topol J, Sullivan JL.
    Prog Clin Biol Res; 1982 May; 95():33-65. PubMed ID: 6289358
    [No Abstract] [Full Text] [Related]

  • 5. [Biological diagnosis of Gaucher's disease].
    Berhoune A, Zenati A, Bellahsene Z, Khiari M, Maiza H, Zighout M, Khati S, Oukaci Y, Khati B.
    Tunis Med; 1980 May; 58(1-2):452-7. PubMed ID: 6782723
    [No Abstract] [Full Text] [Related]

  • 6. Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease.
    Hollak CE, van Weely S, van Oers MH, Aerts JM.
    J Clin Invest; 1994 Mar; 93(3):1288-92. PubMed ID: 8132768
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  • 7. [Plasma chitotriosidase activity in Argentinian patients with Gaucher disease, various lysosomal diseases and other inherited metabolic disorders].
    Dodelson de Kremer R, Paschini de Capra A, Angaroni CJ, Giner de Ayala A.
    Medicina (B Aires); 1997 Mar; 57(6):677-84. PubMed ID: 9674188
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  • 10. Homozygote and heterozygote identification.
    Wenger DA, Roth S.
    Prog Clin Biol Res; 1982 Mar; 95():551-72. PubMed ID: 6812086
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  • 11. Gaucher type I (Ashkenazi) disease: considerations for heterozygote detection and prenatal diagnosis.
    Grabowski GA, Dinur T, Gatt S, Desnick RJ.
    Prog Clin Biol Res; 1982 Mar; 95():573-95. PubMed ID: 6812087
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  • 14. Plasma lipids are altered in Gaucher disease: biochemical markers to evaluate therapeutic intervention.
    Meikle PJ, Whitfield PD, Rozaklis T, Blacklock D, Duplock S, Elstein D, Zimran A, Mengel E, Cannell P, Hopwood JJ, Fuller M.
    Blood Cells Mol Dis; 2008 Mar; 40(3):420-7. PubMed ID: 18054258
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  • 18. Application of a comprehensive protocol for the identification of Gaucher disease in Brazil.
    Michelin K, Wajner A, de Souza FT, de Mello AS, Burin MG, Pereira ML, Pires RF, Giugliani R, Coelho JC.
    Am J Med Genet A; 2005 Jul 01; 136(1):58-62. PubMed ID: 15937950
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  • 20. Gaucher's disease: a clinical, morphological and biochemical study of a Nigerian family.
    Johnson AO, Glew RH, Williams AO.
    Afr J Med Med Sci; 1980 Jul 01; 9(1-2):27-36. PubMed ID: 6282083
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