BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 18198629)

  • 1. [Congenital disorders of glycosylation and project "Euroglycanet"].
    Petković D; Bilić K; Ninković D; Cuk M; Fumić K; Barić I
    Lijec Vjesn; 2007; 129(8-9):286-92. PubMed ID: 18198629
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mass spectrometry for congenital disorders of glycosylation, CDG.
    Wada Y
    J Chromatogr B Analyt Technol Biomed Life Sci; 2006 Jun; 838(1):3-8. PubMed ID: 16517226
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Congenital disorders of N-glycosylation including diseases associated with O- as well as N-glycosylation defects.
    Leroy JG
    Pediatr Res; 2006 Dec; 60(6):643-56. PubMed ID: 17065563
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening and diagnosis of congenital disorders of glycosylation.
    Marklová E; Albahri Z
    Clin Chim Acta; 2007 Oct; 385(1-2):6-20. PubMed ID: 17716641
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Altered glycan structures: the molecular basis of congenital disorders of glycosylation.
    Freeze HH; Aebi M
    Curr Opin Struct Biol; 2005 Oct; 15(5):490-8. PubMed ID: 16154350
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Congenital disorders of glycosylation].
    Durand G; Dupré T; Vuillaumier-Barrot S; Seta N
    Ann Pharm Fr; 2003; 61(5):330-9. PubMed ID: 13130291
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylation.
    Cohn RD; Eklund E; Bergner AL; Casella JF; Woods SL; Althaus J; Blakemore KJ; Fox HE; Hoover-Fong JE; Hamosh A; Braverman NE; Freeze HH; Boyadjiev SA
    Pediatrics; 2006 Aug; 118(2):e514-21. PubMed ID: 16816004
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital disorders of glycosylation: glycosylation defects in man and biological models for their study.
    Marquardt T; Freeze H
    Biol Chem; 2001 Feb; 382(2):161-77. PubMed ID: 11308015
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups.
    Wopereis S; Morava E; Grünewald S; Adamowicz M; Huijben KM; Lefeber DJ; Wevers RA
    Glycobiology; 2005 Dec; 15(12):1312-9. PubMed ID: 16037491
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Molecular diagnosis of congenital disorders of glycosylation].
    Vuillaumier-Barrot S
    Ann Biol Clin (Paris); 2005; 63(2):135-43. PubMed ID: 15771971
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A rapid mass spectrometric strategy for the characterization of N- and O-glycan chains in the diagnosis of defects in glycan biosynthesis.
    Faid V; Chirat F; Seta N; Foulquier F; Morelle W
    Proteomics; 2007 Jun; 7(11):1800-13. PubMed ID: 17520685
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Defective protein glycosylation in patients with cutis laxa syndrome.
    Morava E; Wopereis S; Coucke P; Gillessen-Kaesbach G; Voit T; Smeitink J; Wevers R; Grünewald S
    Eur J Hum Genet; 2005 Apr; 13(4):414-21. PubMed ID: 15657616
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Cardiomyopathy in congenital disorders of glycosylation.
    Gehrmann J; Sohlbach K; Linnebank M; Böhles HJ; Buderus S; Kehl HG; Vogt J; Harms E; Marquardt T
    Cardiol Young; 2003 Aug; 13(4):345-51. PubMed ID: 14694955
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Congenital disorder of glycosylation-X: clinicopathologic study of an autopsy case with distinct neuropathologic features.
    Agarwal B; Ahmed A; Rushing EJ; Bloom M; Kadom N; Vezina G; Krasnewich D; Santi M
    Hum Pathol; 2007 Nov; 38(11):1714-9. PubMed ID: 17954208
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Congenital disorders of glycosylation: rapidly enlarging group of (neuro)metabolic disorders.
    Grünewald S
    Early Hum Dev; 2007 Dec; 83(12):825-30. PubMed ID: 17959325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening for congenital disorders of glycosylation (CDG): transferrin HPLC versus isoelectric focusing (IEF).
    Quintana E; Navarro-Sastre A; Hernández-Pérez JM; García-Villoria J; Montero R; Artuch R; Ribes A; Briones P
    Clin Biochem; 2009 Mar; 42(4-5):408-15. PubMed ID: 19146845
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mass spectrometry in the characterization of human genetic N-glycosylation defects.
    Barone R; Sturiale L; Garozzo D
    Mass Spectrom Rev; 2009; 28(3):517-42. PubMed ID: 18844296
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Congenital disorders of glycosylation. Their diagnosis and treatment].
    Pérez-Cerdá C; Ugarte M
    Rev Neurol; 2006 Oct; 43 Suppl 1():S145-56. PubMed ID: 17061182
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Recurrent thrombo-embolism in a child with a congenital disorder of glycosylation (CDG) type Ib and treatment with mannose.
    Tamminga RY; Lefeber DJ; Kamps WA; van Spronsen FJ
    Pediatr Hematol Oncol; 2008 Dec; 25(8):762-8. PubMed ID: 19065443
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.