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Volumn 134, Issue 1, 2014, Pages

Successful liver transplantation and long-term follow-up in a patient with MPI-CDG

Author keywords

Congenital disorder of glycosylation; Liver transplantation; MPI CDG

Indexed keywords

ANTIBIOTIC AGENT; MANNOSE; MANNOSE PHOSPHATE ISOMERASE; MORPHINE;

EID: 84904100059     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2013-2732     Document Type: Article
Times cited : (50)

References (11)
  • 1
    • 78650401291 scopus 로고    scopus 로고
    • Congenital disorders of glycosylation
    • Jaeken J. Congenital disorders of glycosylation. Ann N Y Acad Sci. 2010;1214:190-198
    • (2010) Ann N Y Acad Sci , vol.1214 , pp. 190-198
    • Jaeken, J.1
  • 2
    • 80955145770 scopus 로고    scopus 로고
    • Congenital disorders of glycosylation: Sweet news
    • Theodore M, Morava E. Congenital disorders of glycosylation: sweet news. Curr Opin Pediatr. 2011;23(6):581-587
    • (2011) Curr Opin Pediatr , vol.23 , Issue.6 , pp. 581-587
    • Theodore, M.1    Morava, E.2
  • 3
    • 79961169660 scopus 로고    scopus 로고
    • How to find and diagnose a CDG due to defective N-glycosylation
    • Lefeber DJ, Morava E, Jaeken J. How to find and diagnose a CDG due to defective N-glycosylation. J Inherit Metab Dis. 2011;34(4):849-852
    • (2011) J Inherit Metab Dis , vol.34 , Issue.4 , pp. 849-852
    • Lefeber, D.J.1    Morava, E.2    Jaeken, J.3
  • 4
    • 70249148051 scopus 로고    scopus 로고
    • The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib
    • de Lonlay P, Seta N. The clinical spectrum of phosphomannose isomerase deficiency, with an evaluation of mannose treatment for CDG-Ib. Biochim Biophys Acta. 2009;1792(9):841-843
    • (2009) Biochim Biophys Acta , vol.1792 , Issue.9 , pp. 841-843
    • De Lonlay, P.1    Seta, N.2
  • 5
    • 0035718934 scopus 로고    scopus 로고
    • Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: Long-term outcome and effects of mannose supplementation
    • DOI 10.1006/mgme.2001.3161
    • Westphal V, Kjaergaard S, Davis JA, Peterson SM, Skovby F, Freeze HH. Genetic and metabolic analysis of the first adult with congenital disorder of glycosylation type Ib: long-term outcome and effects of mannose supplementation. Mol Genet Metab. 2001;73(1):77-85 (Pubitemid 34177627)
    • (2001) Molecular Genetics and Metabolism , vol.73 , Issue.1 , pp. 77-85
    • Westphal, V.1    Kjaergaard, S.2    Davis, J.A.3    Peterson, S.M.4    Skovby, F.5    Freeze, H.H.6
  • 8
    • 34447130291 scopus 로고    scopus 로고
    • The liver in congenital disorders of glycosylation: Ultrastructural features
    • DOI 10.1080/01913120701348286, PII 779833797
    • Iancu TC, Mahajnah M, Manov I, Cherurg S, Knopf C, Mandel H. The liver in congenital disorders of glycosylation: ultrastructural features. Ultrastruct Pathol. 2007;31(3):189-197 (Pubitemid 47037189)
    • (2007) Ultrastructural Pathology , vol.31 , Issue.3 , pp. 189-197
    • Iancu, T.C.1    Mahajnah, M.2    Manov, I.3    Cherurg, S.4    Knopf, C.5    Mandel, H.6
  • 11
    • 84879464716 scopus 로고    scopus 로고
    • From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG)
    • Kapusta L, Zucker N, Frenckel G, et al. From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG). Heart Fail Rev. 2013;18(2):187-196
    • (2013) Heart Fail Rev , vol.18 , Issue.2 , pp. 187-196
    • Kapusta, L.1    Zucker, N.2    Frenckel, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.