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Volumn 28, Issue 4, 2005, Pages 575-583

Enzyme replacement therapy in Japanese Fabry disease patients: The results of a phase 2 bridging study

Author keywords

[No Author keywords available]

Indexed keywords

AGALSIDASE BETA; GLOBOTRIAOSYLCERAMIDE; HYDROXYZINE; IBUPROFEN; IMMUNOGLOBULIN G ANTIBODY; PARACETAMOL;

EID: 19944375153     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-005-0575-y     Document Type: Article
Times cited : (46)

References (13)
  • 1
    • 0035238463 scopus 로고    scopus 로고
    • Fabry disease: Clinical features and recent advances in enzyme replacement therapy
    • Desnick RJ, Wasserstein MP (2001) Fabry disease: Clinical features and recent advances in enzyme replacement therapy. Adv Nephrol Necker Hosp 31: 317-339.
    • (2001) Adv. Nephrol. Necker Hosp. , vol.31 , pp. 317-339
    • Desnick, R.J.1    Wasserstein, M.P.2
  • 2
    • 0000889058 scopus 로고    scopus 로고
    • α-Galactosidase A deficiency: Fabry disease
    • Scriver CR, Beaudet AL, Sly WS, Valle D, eds; Childs B, Kinzler KW, Vogelstein B, assoc. eds. 8th edn. New York: McGraw-Hill
    • Desnick RJ, Ioannou YA, Eng CM (2001) α-Galactosidase A deficiency: Fabry disease. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds; Childs B, Kinzler KW, Vogelstein B, assoc. eds. The Metabolic and Molecular Bases of Inherited Disease, 8th edn. New York: McGraw-Hill, 3733-3774.
    • (2001) The Metabolic and Molecular Bases of Inherited Disease , pp. 3733-3774
    • Desnick, R.J.1    Ioannou, Y.A.2    Eng, C.M.3
  • 3
    • 0025049304 scopus 로고
    • Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy
    • Elleder M, Bradova V, Smid F, et al (1990) Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy. Virchows Arch A Pathol Anat Histopathol 417(5): 449-455.
    • (1990) Virchows Arch. A Pathol. Anat. Histopathol. , vol.417 , Issue.5 , pp. 449-455
    • Elleder, M.1    Bradova, V.2    Smid, F.3
  • 4
    • 0035097499 scopus 로고    scopus 로고
    • A phase 1/2 clinical trial of enzyme replacement in Fabry disease: Pharmacokinetic, substrate clearance, and safety studies
    • Eng CM, Banikazemi M, Gordon RE, et al (2001a) A phase 1/2 clinical trial of enzyme replacement in Fabry disease: Pharmacokinetic, substrate clearance, and safety studies. Am J Hum Genet 68(3): 711-722.
    • (2001) Am. J. Hum. Genet. , vol.68 , Issue.3 , pp. 711-722
    • Eng, C.M.1    Banikazemi, M.2    Gordon, R.E.3
  • 5
    • 0035811624 scopus 로고    scopus 로고
    • Safety and efficacy of recombinant human α-galactosidase A replacement therapy in Fabry's disease
    • Eng CM, Guffon N, Wilcox WR, et al (2001b) Safety and efficacy of recombinant human α-galactosidase A replacement therapy in Fabry's disease. N Engl J Med 345(1): 9-16.
    • (2001) N. Engl. J. Med. , vol.345 , Issue.1 , pp. 9-16
    • Eng, C.M.1    Guffon, N.2    Wilcox, W.R.3
  • 6
    • 0036266968 scopus 로고    scopus 로고
    • Anderson-Fabry disease: Extrarenal, neurologic manifestations
    • Kolodny EH, Pastores GM (2002) Anderson-Fabry disease: Extrarenal, neurologic manifestations. J Am Soc Nephrol 13(supplement 2): S150-153.
    • (2002) J. Am. Soc. Nephrol. , vol.13 , Issue.SUPPL. 2
    • Kolodny, E.H.1    Pastores, G.M.2
  • 8
    • 0036981036 scopus 로고    scopus 로고
    • X-chromosome inactivation and human genetic disease
    • Lyon MF (2002) X-chromosome inactivation and human genetic disease. Acta Paediatr Suppl 91(439): 107-112.
    • (2002) Acta Paediatr. Suppl. , vol.91 , Issue.439 , pp. 107-112
    • Lyon, M.F.1
  • 9
    • 0033585476 scopus 로고    scopus 로고
    • Prevalence of lysosomal storage disorders
    • Meikle PJ, Hopwood JJ, Clague AE, et al (1999) Prevalence of lysosomal storage disorders. JAMA 281(3): 249-254.
    • (1999) JAMA , vol.281 , Issue.3 , pp. 249-254
    • Meikle, P.J.1    Hopwood, J.J.2    Clague, A.E.3
  • 10
    • 12444319931 scopus 로고    scopus 로고
    • Fabry disease: Detection of undiagnosed hemodialysis patients and identification of a 'renal variant' phenotype
    • Nakao S, Kodama C, Takenaka T, et al (2003) Fabry disease: Detection of undiagnosed hemodialysis patients and identification of a 'renal variant' phenotype. Kidney Int 64(3): 801-807.
    • (2003) Kidney Int. , vol.64 , Issue.3 , pp. 801-807
    • Nakao, S.1    Kodama, C.2    Takenaka, T.3
  • 11
    • 0026099642 scopus 로고
    • An atypical variant of Fabry's disease with manifestations confined to the myocardium
    • von Scheidt W, Eng CM, Fitzmaurice TF, et al (1991) An atypical variant of Fabry's disease with manifestations confined to the myocardium. N Engl J Med 324(6): 395-399.
    • (1991) N. Engl. J. Med. , vol.324 , Issue.6 , pp. 395-399
    • von Scheidt, W.1    Eng, C.M.2    Fitzmaurice, T.F.3
  • 12
    • 12944265457 scopus 로고    scopus 로고
    • Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease
    • Schiffmann R, Murray GJ, Treco D, et al (2000) Infusion of alpha-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease. Proc Natl Acad Sci USA 97(1): 365-370.
    • (2000) Proc. Natl. Acad. Sci. USA , vol.97 , Issue.1 , pp. 365-370
    • Schiffmann, R.1    Murray, G.J.2    Treco, D.3
  • 13
    • 0035816007 scopus 로고    scopus 로고
    • Enzyme replacement therapy in Fabry disease: A randomized controlled trial
    • Schiffmann R, Kopp JB, Austin HA 3rd, et al (2001) Enzyme replacement therapy in Fabry disease: A randomized controlled trial. JAMA 285(21): 2743-2749.
    • (2001) JAMA , vol.285 , Issue.21 , pp. 2743-2749
    • Schiffmann, R.1    Kopp, J.B.2    Austin III, H.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.