메뉴 건너뛰기




Volumn 327, Issue 7413, 2003, Pages 462-463

Treatment of lysosomal storage disorders

Author keywords

[No Author keywords available]

Indexed keywords

AGALSIDASE ALFA; AGALSIDASE BETA; GLUCOSYLCERAMIDASE; IMIGLUCERASE; MIGLUSTAT;

EID: 0041352256     PISSN: 09598146     EISSN: None     Source Type: Journal    
DOI: 10.1136/bmj.327.7413.462     Document Type: Editorial
Times cited : (21)

References (9)
  • 2
    • 0036796821 scopus 로고    scopus 로고
    • New developments in the management of Anderson-Fabry disease
    • Mehta A. New developments in the management of Anderson-Fabry disease. QJ Med 2002;95:647-53.
    • (2002) QJ Med , vol.95 , pp. 647-653
    • Mehta, A.1
  • 3
    • 0041700972 scopus 로고    scopus 로고
    • Lysosomal storage disorders: Prevalence and newborn screening
    • Meikle PJ, Hopwood JJ. Lysosomal storage disorders: Prevalence and newborn screening. Gaucher Clin Perspect 2000;8:1-5.
    • (2000) Gaucher Clin Perspect , vol.8 , pp. 1-5
    • Meikle, P.J.1    Hopwood, J.J.2
  • 4
    • 0035816007 scopus 로고    scopus 로고
    • Enzyme replacement therapy in Fabry disease: A randomized controlled trial
    • Schiffmann R, Kopp JB, Austin HA 3rd, Sabnis S, Moore DF, Weibel T, et al. Enzyme replacement therapy in Fabry disease: a randomized controlled trial. JAMA 2001;285:2743-9.
    • (2001) JAMA , vol.285 , pp. 2743-2749
    • Schiffmann, R.1    Kopp, J.B.2    Austin H.A. III3    Sabnis, S.4    Moore, D.F.5    Weibel, T.6
  • 5
    • 0035811624 scopus 로고    scopus 로고
    • Safety and efficacy of recombinant human α-galactosidase A replacement in Fabry's disease
    • Eng CM, Guffon N, Wilcox WR, Germain DP, Lee P, Waldek S, et al. Safety and efficacy of recombinant human α-galactosidase A replacement in Fabry's disease. N Engl J Med 2001;345:9-16.
    • (2001) N Engl J Med , vol.345 , pp. 9-16
    • Eng, C.M.1    Guffon, N.2    Wilcox, W.R.3    Germain, D.P.4    Lee, P.5    Waldek, S.6
  • 6
    • 0035949059 scopus 로고    scopus 로고
    • Enzyme replacement therapy for Anderson-Fabry disease
    • Pastores GM, Thadhani R. Enzyme replacement therapy for Anderson-Fabry disease. Lancet 2001;358:601-3.
    • (2001) Lancet , vol.358 , pp. 601-603
    • Pastores, G.M.1    Thadhani, R.2
  • 7
    • 0037177166 scopus 로고    scopus 로고
    • Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy
    • Sachdev B, Takenaka T, Teraguchi H, Tei C, Lee P, McKenna WJ, et al. Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy. Circulation 2002;105:1407-11.
    • (2002) Circulation , vol.105 , pp. 1407-1411
    • Sachdev, B.1    Takenaka, T.2    Teraguchi, H.3    Tei, C.4    Lee, P.5    McKenna, W.J.6
  • 8
    • 0023758733 scopus 로고
    • Anderson-Fabry disease: A commonly missed diagnosis
    • Morgan SH, Crawford d'A. Anderson-Fabry disease: a commonly missed diagnosis. BMJ 1988;297:872-3.
    • (1988) BMJ , vol.297 , pp. 872-873
    • Morgan, S.H.1    Crawford, D'A.2
  • 9
    • 0034728914 scopus 로고    scopus 로고
    • A novel treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis
    • Cox T, Lachmann R, Hollak C, Aerts J, van Weely S, Hrebicek M, et al. A novel treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis. Lancet 2000;355:1481-5.
    • (2000) Lancet , vol.355 , pp. 1481-1485
    • Cox, T.1    Lachmann, R.2    Hollak, C.3    Aerts, J.4    Van Weely, S.5    Hrebicek, M.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.