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Journal Abstract Search

138 related items for PubMed ID: 19819171

  • 1. CCL18 as an alternative marker in Gaucher and Niemann-Pick disease with chitotriosidase deficiency.
    Chang KL, Hwu WL, Yeh HY, Lee NC, Chien YH.
    Blood Cells Mol Dis; 2010 Jan 15; 44(1):38-40. PubMed ID: 19819171
    [No Abstract] [Full Text] [Related]

  • 2. Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick disease.
    Brinkman J, Wijburg FA, Hollak CE, Groener JE, Verhoek M, Scheij S, Aten J, Boot RG, Aerts JM.
    J Inherit Metab Dis; 2005 Jan 15; 28(1):13-20. PubMed ID: 15702402
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  • 3. Plasma chitotriosidase and CCL18 as surrogate markers for granulomatous macrophages in sarcoidosis.
    Boot RG, Hollak CE, Verhoek M, Alberts C, Jonkers RE, Aerts JM.
    Clin Chim Acta; 2010 Jan 15; 411(1-2):31-6. PubMed ID: 19808030
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  • 4. Plasma chitotriosidase activity versus CCL18 level for assessing type I Gaucher disease severity: protocol for a systematic review with meta-analysis of individual participant data.
    Raskovalova T, Deegan PB, Yang R, Pavlova E, Stirnemann J, Labarère J, Zimran A, Mistry PK, Berger M.
    Syst Rev; 2017 Apr 20; 6(1):87. PubMed ID: 28427477
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  • 5. Hematopoietic stem cell transplantation in Niemann-Pick disease type B monitored by chitotriosidase activity.
    Quarello P, Spada M, Porta F, Vassallo E, Timeus F, Fagioli F.
    Pediatr Blood Cancer; 2018 Feb 20; 65(2):. PubMed ID: 29090525
    [Abstract] [Full Text] [Related]

  • 6. Elevated plasma chemokine CCL18/PARC in beta-thalassemia.
    Dimitriou E, Verhoek M, Altun S, Karabatsos F, Moraitou M, Youssef J, Boot R, Sarafidou J, Karagiorga M, Aerts H, Michelakakis H.
    Blood Cells Mol Dis; 2005 Feb 20; 35(3):328-31. PubMed ID: 16137900
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  • 7. Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention.
    Boot RG, Verhoek M, de Fost M, Hollak CE, Maas M, Bleijlevens B, van Breemen MJ, van Meurs M, Boven LA, Laman JD, Moran MT, Cox TM, Aerts JM.
    Blood; 2004 Jan 01; 103(1):33-9. PubMed ID: 12969956
    [Abstract] [Full Text] [Related]

  • 8. Critical assessment of chitotriosidase analysis in the rational laboratory diagnosis of children with Gaucher disease and Niemann-Pick disease type A/B and C.
    Ries M, Schaefer E, Lührs T, Mani L, Kuhn J, Vanier MT, Krummenauer F, Gal A, Beck M, Mengel E.
    J Inherit Metab Dis; 2006 Oct 01; 29(5):647-52. PubMed ID: 16972172
    [Abstract] [Full Text] [Related]

  • 9. [Current and future biochemical markers for Gaucher disease].
    Froissart R.
    Rev Med Interne; 2006 Mar 01; 27 Suppl 1():S22-5. PubMed ID: 16644397
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  • 16. Quantitation of plasmatic lysosphingomyelin and lysosphingomyelin-509 for differential screening of Niemann-Pick A/B and C diseases.
    Kuchar L, Sikora J, Gulinello ME, Poupetova H, Lugowska A, Malinova V, Jahnova H, Asfaw B, Ledvinova J.
    Anal Biochem; 2017 May 15; 525():73-77. PubMed ID: 28259515
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  • 19. Utility of amniotic fluid chitotriosidase in the prenatal diagnosis of lysosomal storage disorders.
    Kadali S, Madalasa T, Reddy GM, Naushad SM.
    Clin Biochem; 2018 Nov 15; 61():40-44. PubMed ID: 30205089
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  • 20. Biochemical characterization of chitotriosidase enzyme: comparison between normal individuals and patients with Gaucher and with Niemann-Pick diseases.
    Wajner A, Michelin K, Burin MG, Pires RF, Pereira ML, Giugliani R, Coelho JC.
    Clin Biochem; 2004 Oct 15; 37(10):893-7. PubMed ID: 15369720
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