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.
91 related articles for article (PubMed ID: 16860006)
1. Identification of chitotriosidase isoforms in plasma of Gaucher disease patients by two dimensional gel electrophoresis. Quintana L; Monasterio A; Escuredo K; del Amo J; Alfonso P; Elortza F; Santa Cruz S; Simón L; Martínez A; Giraldo P; Pocoví M; Castrillo JL Biochim Biophys Acta; 2006 Jul; 1764(7):1292-8. PubMed ID: 16860006 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. [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]
4. Chitotriosidase on treatment-naïve patients with Gaucher disease: A genotype vs phenotype study. Sperb-Ludwig F; Heineck BL; Michelin-Tirelli K; Alegra T; Schwartz IVD Clin Chim Acta; 2019 May; 492():1-6. PubMed ID: 30695688 [TBL] [Abstract][Full Text] [Related]
5. Chitotriosidase genotype and plasma activity in patients type 1 Gaucher's disease and their relatives (carriers and non carriers). Giraldo P; Cenarro A; Alfonso P; Pérez-Calvo JI; Rubio-Félix D; Giralt M; Pocoví M Haematologica; 2001 Sep; 86(9):977-84. PubMed ID: 11532627 [TBL] [Abstract][Full Text] [Related]
6. 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; 6(1):87. PubMed ID: 28427477 [TBL] [Abstract][Full Text] [Related]
7. Mass spectrometric quantification of glucosylsphingosine in plasma and urine of type 1 Gaucher patients using an isotope standard. Mirzaian M; Wisse P; Ferraz MJ; Gold H; Donker-Koopman WE; Verhoek M; Overkleeft HS; Boot RG; Kramer G; Dekker N; Aerts JM Blood Cells Mol Dis; 2015 Apr; 54(4):307-14. PubMed ID: 25842368 [TBL] [Abstract][Full Text] [Related]
8. [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]
9. 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 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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; 37(10):893-7. PubMed ID: 15369720 [TBL] [Abstract][Full Text] [Related]
12. Comparison between the biochemical properties of plasma chitotriosidase from normal individuals and from patients with Gaucher disease, GM1-gangliosidosis, Krabbe disease and heterozygotes for Gaucher disease. Wajner A; Michelin K; Burin MG; Pires RF; Pereira ML; Giugliani R; Coelho JC Clin Biochem; 2007 Mar; 40(5-6):365-9. PubMed ID: 17291472 [TBL] [Abstract][Full Text] [Related]
13. [Diagnosis, biomarkers and biochemical alterations in Gaucher's disease]. Gort L; Coll MJ Med Clin (Barc); 2011 Sep; 137 Suppl 1():12-6. PubMed ID: 22230120 [TBL] [Abstract][Full Text] [Related]
14. The biology of the Gaucher cell: the cradle of human chitinases. Bussink AP; van Eijk M; Renkema GH; Aerts JM; Boot RG Int Rev Cytol; 2006; 252():71-128. PubMed ID: 16984816 [TBL] [Abstract][Full Text] [Related]
15. Type 1 Gaucher disease: null and hypomorphic novel chitotriosidase mutations-implications for diagnosis and therapeutic monitoring. Grace ME; Balwani M; Nazarenko I; Prakash-Cheng A; Desnick RJ Hum Mutat; 2007 Sep; 28(9):866-73. PubMed ID: 17464953 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Biochemical and Molecular Chitotriosidase Profiles in Patients with Gaucher Disease Type 1 in Minas Gerais, Brazil: New Mutation in CHIT1 Gene. Adelino TER; Martins GG; Gomes AAA; Torres AA; Silva DAS; Xavier VDO; Guimarães JPO; Araújo SSS; Fernandes RAF; Oliveira MCLA; Godard ALB; Valadares ER JIMD Rep; 2013; 9():85-91. PubMed ID: 23430552 [TBL] [Abstract][Full Text] [Related]