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 *

141 related articles for article (PubMed ID: 24359113)

  • 1. N-glycan abnormalities in children with galactosemia.
    Coss KP; Hawkes CP; Adamczyk B; Stöckmann H; Crushell E; Saldova R; Knerr I; Rubio-Gozalbo ME; Monavari AA; Rudd PM; Treacy EP
    J Proteome Res; 2014 Feb; 13(2):385-94. PubMed ID: 24359113
    [TBL] [Abstract][Full Text] [Related]  

  • 2. IgG N-glycans as potential biomarkers for determining galactose tolerance in Classical Galactosaemia.
    Coss KP; Byrne JC; Coman DJ; Adamczyk B; Abrahams JL; Saldova R; Brown AY; Walsh O; Hendroff U; Carolan C; Rudd PM; Treacy EP
    Mol Genet Metab; 2012 Feb; 105(2):212-20. PubMed ID: 22133299
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Galactosemia, a single gene disorder with epigenetic consequences.
    Coman DJ; Murray DW; Byrne JC; Rudd PM; Bagaglia PM; Doran PD; Treacy EP
    Pediatr Res; 2010 Mar; 67(3):286-92. PubMed ID: 19952866
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia.
    Sturiale L; Barone R; Fiumara A; Perez M; Zaffanello M; Sorge G; Pavone L; Tortorelli S; O'Brien JF; Jaeken J; Garozzo D
    Glycobiology; 2005 Dec; 15(12):1268-76. PubMed ID: 16037488
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Galactose breath testing distinguishes variant and severe galactose-1-phosphate uridyltransferase genotypes.
    Berry GT; Singh RH; Mazur AT; Guerrero N; Kennedy MJ; Chen J; Reynolds R; Palmieri MJ; Klein PD; Segal S; Elsas LJ
    Pediatr Res; 2000 Sep; 48(3):323-8. PubMed ID: 10960497
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effects of temporary low-dose galactose supplements in children aged 5-12 y with classical galactosemia: a pilot study.
    Knerr I; Coss KP; Kratzsch J; Crushell E; Clark A; Doran P; Shin Y; Stöckmann H; Rudd PM; Treacy E
    Pediatr Res; 2015 Sep; 78(3):272-9. PubMed ID: 26053138
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Classical galactosaemia: novel insights in IgG N-glycosylation and N-glycan biosynthesis.
    Maratha A; Stockmann H; Coss KP; Estela Rubio-Gozalbo M; Knerr I; Fitzgibbon M; McVeigh TP; Foley P; Moss C; Colhoun HO; van Erven B; Stephens K; Doran P; Rudd P; Treacy E
    Eur J Hum Genet; 2016 Jul; 24(7):976-84. PubMed ID: 26733289
    [TBL] [Abstract][Full Text] [Related]  

  • 8. N- and O-linked glycosylation of total plasma glycoproteins in galactosemia.
    Liu Y; Xia B; Gleason TJ; Castañeda U; He M; Berry GT; Fridovich-Keil JL
    Mol Genet Metab; 2012 Aug; 106(4):442-54. PubMed ID: 22743281
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiplexed glycoproteomic analysis of glycosylation disorders by sequential yolk immunoglobulins immunoseparation and MALDI-TOF MS.
    Sturiale L; Barone R; Palmigiano A; Ndosimao CN; Briones P; Adamowicz M; Jaeken J; Garozzo D
    Proteomics; 2008 Sep; 8(18):3822-32. PubMed ID: 18712764
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of common mutations in the GALT gene through ARMS.
    Mahmood U; Imran M; Naik SI; Cheema HA; Saeed A; Arshad M; Mahmood S
    Gene; 2012 Nov; 509(2):291-4. PubMed ID: 22963887
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Validation of an automated ultraperformance liquid chromatography IgG N-glycan analytical method applicable to classical galactosaemia.
    Colhoun HO; Treacy EP; MacMahon M; Rudd PM; Fitzgibbon M; O'Flaherty R; Stepien KM
    Ann Clin Biochem; 2018 Sep; 55(5):593-603. PubMed ID: 29444593
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Abnormal
    Treacy EP; Vencken S; Bosch AM; Gautschi M; Rubio-Gozalbo E; Dawson C; Nerney D; Colhoun HO; Shakerdi L; Pastores GM; O'Flaherty R; Saldova R
    JIMD Rep; 2021 Sep; 61(1):76-88. PubMed ID: 34485021
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Serum markers of bone turnover in children and adolescents with classic galactosemia.
    Gajewska J; Ambroszkiewicz J; Radomyska B; Chełchowska M; Ołtarzewski M; Laskowska-Klita T; Milanowski A
    Adv Med Sci; 2008; 53(2):214-20. PubMed ID: 18650146
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Differential glycomics of epithelial membrane glycoproteins from urinary exovesicles reveals shifts toward complex-type N-glycosylation in classical galactosemia.
    Staubach S; Schadewaldt P; Wendel U; Nohroudi K; Hanisch FG
    J Proteome Res; 2012 Feb; 11(2):906-16. PubMed ID: 22087537
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fertility in classical galactosaemia, a study of N-glycan, hormonal and inflammatory gene interactions.
    Colhoun HO; Rubio Gozalbo EM; Bosch AM; Knerr I; Dawson C; Brady J; Galligan M; Stepien K; O'Flaherty R; Catherine Moss C; Peter Barker P; Fitzgibbon M; Doran PP; Treacy EP
    Orphanet J Rare Dis; 2018 Sep; 13(1):164. PubMed ID: 30231941
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cognitive strengths and weaknesses in children and adolescents homozygous for the galactosemia Q188R mutation: a descriptive study.
    Antshel KM; Epstein IO; Waisbren SE
    Neuropsychology; 2004 Oct; 18(4):658-64. PubMed ID: 15506833
    [TBL] [Abstract][Full Text] [Related]  

  • 17. IgG N-Glycosylation Galactose Incorporation Ratios for the Monitoring of Classical Galactosaemia.
    Stockmann H; Coss KP; Rubio-Gozalbo ME; Knerr I; Fitzgibbon M; Maratha A; Wilson J; Rudd P; Treacy EP
    JIMD Rep; 2016; 27():47-53. PubMed ID: 26419375
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital disorders of glycosylation.
    Jaeken J; Matthijs G
    Annu Rev Genomics Hum Genet; 2001; 2():129-51. PubMed ID: 11701646
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Long-term complications in Estonian galactosemia patients with a less strict lactose-free diet and metabolic control.
    Krabbi K; Uudelepp ML; Joost K; Zordania R; Õunap K
    Mol Genet Metab; 2011 Jul; 103(3):249-53. PubMed ID: 21501963
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The first study of galactose-1-phosphate uridyl transferase mutations in Iranian galactosemia patients.
    Mirzajani F; Mirfakhraie R; Nabati F; Tabatabaei NN; Talachian E; Houshmand M
    Clin Biochem; 2006 Jul; 39(7):697-9. PubMed ID: 16765930
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.