These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 19936666)

  • 1. Plasma chitotriosidase activity in children with lysosomal storage disorders.
    Sheth JJ; Sheth FJ; Oza NJ; Gambhir PS; Dave UP; Shah RC
    Indian J Pediatr; 2010 Feb; 77(2):203-5. PubMed ID: 19936666
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 61():40-44. PubMed ID: 30205089
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 29(5):647-52. PubMed ID: 16972172
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Comparison and clinical application of two methods for determination of plasma chitotriosidase activity].
    Wang Y; Zhang HW; Ye J; Qiu WJ; Han LS; Gu XF
    Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):834-8. PubMed ID: 23302614
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Lysosomal Storage Disorders in Indian Children with Neuroregression Attending a Genetic Center.
    Sheth J; Mistri M; Bhavsar R; Sheth F; Kamate M; Shah H; Datar C
    Indian Pediatr; 2015 Dec; 52(12):1029-33. PubMed ID: 26713986
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [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; 57(6):677-84. PubMed ID: 9674188
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Oxysterol/chitotriosidase based selective screening for Niemann-Pick type C in infantile cholestasis syndrome patients.
    Degtyareva AV; Proshlyakova TY; Gautier MS; Degtyarev DN; Kamenets EA; Baydakova GV; Rebrikov DV; Zakharova EY
    BMC Med Genet; 2019 Jul; 20(1):123. PubMed ID: 31296176
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical evaluation of chitotriosidase enzyme activity in Gaucher and Niemann Pick A/B diseases: A retrospective study from India.
    Kadali S; Kolusu A; Sunkara S; Gummadi MR; Undamatla J
    Clin Chim Acta; 2016 Jun; 457():8-11. PubMed ID: 26975750
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 28(1):13-20. PubMed ID: 15702402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Elevated plasma chitotriosidase activity in various lysosomal storage disorders.
    Guo Y; He W; Boer AM; Wevers RA; de Bruijn AM; Groener JE; Hollak CE; Aerts JM; Galjaard H; van Diggelen OP
    J Inherit Metab Dis; 1995; 18(6):717-22. PubMed ID: 8750610
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chitotriosidase variants in patients with Gaucher disease. Implications for diagnosis and therapeutic monitoring.
    Irún P; Alfonso P; Aznarez S; Giraldo P; Pocovi M
    Clin Biochem; 2013 Dec; 46(18):1804-7. PubMed ID: 24060732
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Assessment of plasma chitotriosidase activity, CCL18/PARC concentration and NP-C suspicion index in the diagnosis of Niemann-Pick disease type C: a prospective observational study.
    De Castro-Orós I; Irún P; Cebolla JJ; Rodriguez-Sureda V; Mallén M; Pueyo MJ; Mozas P; Dominguez C; Pocoví M;
    J Transl Med; 2017 Feb; 15(1):43. PubMed ID: 28222799
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification and use of biomarkers in Gaucher disease and other lysosomal storage diseases.
    Aerts JM; Hollak CE; van Breemen M; Maas M; Groener JE; Boot RG
    Acta Paediatr Suppl; 2005 Mar; 94(447):43-6; discussion 37-8. PubMed ID: 15895711
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Could GSD type I expand the spectrum of disorders with elevated plasma chitotriosidase activity?
    Tümer L; Kasapkara ÇS; Biberoğlu G; Ezgü F; Hasanoğlu A
    J Pediatr Endocrinol Metab; 2013; 26(11-12):1149-52. PubMed ID: 23813353
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 136(1):58-62. PubMed ID: 15937950
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chitotriosidase activity as additional biomarker in the diagnosis of lysosomal storage diseases.
    Olkhovych NV
    Ukr Biochem J; 2016; 88(1):69-78. PubMed ID: 29227082
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chitotriosidase activity in colostrum from African and Caucasian women.
    Musumeci M; Malaguarnera L; Simpore J; Barone R; Whalen M; Musumeci S
    Clin Chem Lab Med; 2005; 43(2):198-201. PubMed ID: 15843217
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Lysosomal storage disorders.
    Sheth J; Patel P; Sheth F; Shah R
    Indian Pediatr; 2004 Mar; 41(3):260-5. PubMed ID: 15064514
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Serum chitotriosidase, a putative marker of chronically activated macrophages, increases with normal aging.
    Ramanathan R; Kohli A; Ingaramo MC; Jain A; Leng SX; Punjabi NM; Walston JD; Fedarko NS
    J Gerontol A Biol Sci Med Sci; 2013 Oct; 68(10):1303-9. PubMed ID: 23525479
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Follow-up of pre-motor symptoms of Parkinson's disease in adult patients with Gaucher disease type 1 and analysis of their lysosomal enzyme profiles in the CSF.
    Wilke MVMB; Poswar F; Borelli WV; Michelin Tirelli K; Randon DN; Lopes FF; Pasetto FB; Sebastião FM; Iop GD; Faqueti L; da Silva LA; Kubaski F; Schuh AFS; Giugliani R; Schwartz IVD
    Orphanet J Rare Dis; 2023 Oct; 18(1):309. PubMed ID: 37784132
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.