BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 29792046)

  • 1. Fast screening of N-glycosylation disorders by sialotransferrin profiling with capillary zone electrophoresis.
    Kingma HA; van der Sluijs FH; Heiner-Fokkema MR
    Ann Clin Biochem; 2018 Nov; 55(6):693-701. PubMed ID: 29792046
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Screening using serum percentage of carbohydrate-deficient transferrin for congenital disorders of glycosylation in children with suspected metabolic disease.
    Pérez-Cerdá C; Quelhas D; Vega AI; Ecay J; Vilarinho L; Ugarte M
    Clin Chem; 2008 Jan; 54(1):93-100. PubMed ID: 18024528
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A new capillary zone electrophoresis method for the screening of congenital disorders of glycosylation (CDG).
    Parente F; Ah Mew N; Jaeken J; Gilfix BM
    Clin Chim Acta; 2010 Jan; 411(1-2):64-6. PubMed ID: 19840782
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison between high performance liquid chromatography and capillary zone electrophoresis for the diagnosis of congenital disorders of glycosylation.
    Quintana E; Montero R; Casado M; Navarro-Sastre A; Vilaseca MA; Briones P; Artuch R
    J Chromatogr B Analyt Technol Biomed Life Sci; 2009 Aug; 877(24):2513-8. PubMed ID: 19608465
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Diagnosis of congenital disorders of glycosylation by capillary zone electrophoresis of serum transferrin.
    Carchon HA; Chevigné R; Falmagne JB; Jaeken J
    Clin Chem; 2004 Jan; 50(1):101-11. PubMed ID: 14633925
    [TBL] [Abstract][Full Text] [Related]  

  • 6. "Hide and seek": Misleading transferrin variants in PMM2-CDG complicate diagnostics.
    Raynor A; Bruneel A; Vermeersch P; Cholet S; Friedrich S; Eckenweiler M; Schumann A; Hengst S; Tuncel AT; Fenaille F; Thiel C; Rymen D
    Proteomics Clin Appl; 2024 Mar; 18(2):e2300040. PubMed ID: 37876147
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I.
    Guillard M; Wada Y; Hansikova H; Yuasa I; Vesela K; Ondruskova N; Kadoya M; Janssen A; Van den Heuvel LP; Morava E; Zeman J; Wevers RA; Lefeber DJ
    J Inherit Metab Dis; 2011 Aug; 34(4):901-6. PubMed ID: 21431619
    [TBL] [Abstract][Full Text] [Related]  

  • 8. High-resolution capillary zone electrophoresis for transferrin glycoform analysis associated with congenital disorders of glycosylation.
    Tobler M; Caslavska J; Burda P; Thormann W
    J Sep Sci; 2018 Jul; 41(13):2808-2818. PubMed ID: 29701302
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparison of transferrin isoform analysis by capillary electrophoresis and HPLC for screening congenital disorders of glycosylation.
    Dave MB; Dherai AJ; Udani VP; Hegde AU; Desai NA; Ashavaid TF
    J Clin Lab Anal; 2018 Jan; 32(1):. PubMed ID: 28236367
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Capillary zone electrophoresis determination of carbohydrate-deficient transferrin using the new CEofix reagents under high-resolution conditions.
    Joneli J; Lanz C; Thormann W
    J Chromatogr A; 2006 Oct; 1130(2):272-80. PubMed ID: 16777120
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Improved capillary electrophoresis method for the determination of carbohydrate-deficient transferrin in patient sera.
    Lanz C; Kuhn M; Deiss V; Thormann W
    Electrophoresis; 2004 Jul; 25(14):2309-18. PubMed ID: 15274013
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High-resolution mass spectrometry glycoprofiling of intact transferrin for diagnosis and subtype identification in the congenital disorders of glycosylation.
    van Scherpenzeel M; Steenbergen G; Morava E; Wevers RA; Lefeber DJ
    Transl Res; 2015 Dec; 166(6):639-649.e1. PubMed ID: 26307094
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Improvement of CDG diagnosis by combined examination of several glycoproteins.
    Fang J; Peters V; Assmann B; Körner C; Hoffmann GF
    J Inherit Metab Dis; 2004; 27(5):581-90. PubMed ID: 15669673
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new strategy implementing mass spectrometry in the diagnosis of congenital disorders of N-glycosylation (CDG).
    Casetta B; Malvagia S; Funghini S; Martinelli D; Dionisi-Vici C; Barone R; Fiumara A; Donati MA; Guerrini R; la Marca G
    Clin Chem Lab Med; 2020 Aug; 59(1):165-171. PubMed ID: 32776892
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Western blotting with diaminobenzidine detection for the diagnosis of congenital disorders of glycosylation.
    Artuch R; Ferrer I; Pineda J; Moreno J; Busquets C; Briones P; Vilaseca MA
    J Neurosci Methods; 2003 May; 125(1-2):167-71. PubMed ID: 12763243
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Transferrin glycosylation analysis from dried blood spot cards and capillary blood samples.
    Wolking AB; Park JH; Grüneberg M; Reunert J; Fingerhut R; Fobker M; Marquardt T
    J Chromatogr B Analyt Technol Biomed Life Sci; 2019 Feb; 1106-1107():64-70. PubMed ID: 30641270
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Laboratory diagnosis of congenital disorders of glycosylation type I by analysis of transferrin glycoforms.
    Babovic-Vuksanovic D; O'Brien JF
    Mol Diagn Ther; 2007; 11(5):303-11. PubMed ID: 17963418
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Capillary zone electrophoresis with a dynamic double coating for analysis of carbohydrate-deficient transferrin in human serum. Precision performance and pattern recognition.
    Lanz C; Marti U; Thormann W
    J Chromatogr A; 2003 Sep; 1013(1-2):131-47. PubMed ID: 14604115
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation.
    Park JH; Zühlsdorf A; Wada Y; Roll C; Rust S; Du Chesne I; Grüneberg M; Reunert J; Marquardt T
    Clin Chim Acta; 2014 Sep; 436():135-9. PubMed ID: 24875750
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carbohydrate-Deficient Transferrin Determination in a Clinical Setting: Consistency Between Capillary Electrophoresis Assays and Utility of HPLC as a Confirmatory Test.
    Veronesi A; Rota C; Trenti T; Cariani E
    J Clin Lab Anal; 2016 Sep; 30(5):494-9. PubMed ID: 26500068
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.