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Volumn 27, Issue 4, 2004, Pages 499-505

Relief of gastrointestinal symptoms under enzyme replacement therapy in patients with Fabry disease

Author keywords

[No Author keywords available]

Indexed keywords

AGALSIDASE ALFA; ALPHA GALACTOSIDASE;

EID: 4344567983     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:BOLI.0000037342.59612.69     Document Type: Article
Times cited : (57)

References (14)
  • 1
    • 0031764478 scopus 로고    scopus 로고
    • Gastrointestinal symptoms and delayed gastric emptying in Fabry's disease: Response to metoclopramide
    • Argoff CE, Barton NW, Brady RO, Ziessman HA (1998) Gastrointestinal symptoms and delayed gastric emptying in Fabry's disease: response to metoclopramide. Nucl Med Commun 19: 887-891.
    • (1998) Nucl. Med. Commun. , vol.19 , pp. 887-891
    • Argoff, C.E.1    Barton, N.W.2    Brady, R.O.3    Ziessman, H.A.4
  • 2
    • 0035811624 scopus 로고    scopus 로고
    • Safety and efficacy of recombinant human alpha-galactosidase A-replacement therapy in Fabry's disease
    • Eng CM, Guffon N, Wilcox WR, et al (2001) Safety and efficacy of recombinant human alpha-galactosidase A-replacement therapy in Fabry's disease. N Engl J Med 345: 9-16.
    • (2001) N. Engl. J. Med. , vol.345 , pp. 9-16
    • Eng, C.M.1    Guffon, N.2    Wilcox, W.R.3
  • 4
  • 6
    • 0034754467 scopus 로고    scopus 로고
    • Anderson-Fabry disease: Clinical manifestations and impact of disease in a cohort of 60 obligate carrier females
    • MacDermot KD, Holmes A, Miners AH (2001a) Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 60 obligate carrier females. J Med Genet 38: 769-775.
    • (2001) J. Med. Genet. , vol.38 , pp. 769-775
    • MacDermot, K.D.1    Holmes, A.2    Miners, A.H.3
  • 7
    • 0034766525 scopus 로고    scopus 로고
    • Anderson-Fabry disease: Clinical manifestations and impact of disease in a cohort of 98 hemizygous males
    • MacDermot KD, Holmes A, Miners AH (2001b) Anderson-Fabry disease: clinical manifestations and impact of disease in a cohort of 98 hemizygous males. J Med Genet 38: 750-760.
    • (2001) J. Med. Genet. , vol.38 , pp. 750-760
    • MacDermot, K.D.1    Holmes, A.2    Miners, A.H.3
  • 9
    • 0036240872 scopus 로고    scopus 로고
    • Assessment of health-related quality-of-life in males with Anderson Fabry disease before therapeutic intervention
    • Miners AH, Holmes A, Sherr L, Jenkinson C, MacDermot KD (2002) Assessment of health-related quality-of-life in males with Anderson Fabry disease before therapeutic intervention. Qual Life Res 11: 127-133.
    • (2002) Qual. Life Res. , vol.11 , pp. 127-133
    • Miners, A.H.1    Holmes, A.2    Sherr, L.3    Jenkinson, C.4    MacDermot, K.D.5
  • 10
    • 0036234750 scopus 로고    scopus 로고
    • Advances in the management of Anderson-Fabry disease: Enzyme replacement therapy
    • Pastores GH and Thadhani R (2002) Advances in the management of Anderson-Fabry disease: enzyme replacement therapy. Expert Opin Biol Ther 2(3): 325-333.
    • (2002) Expert Opin. Biol. Ther. , vol.2 , Issue.3 , pp. 325-333
    • Pastores, G.H.1    Thadhani, R.2
  • 11
    • 0036326164 scopus 로고    scopus 로고
    • Fabry's disease: Diagnosis in the pediatric age group
    • Pintos Morell G (2002) [Fabry's disease: diagnosis in the pediatric age group]. An Esp Pediatr 57: 45-50.
    • (2002) An. Esp. Pediatr. , vol.57 , pp. 45-50
    • Pintos Morell, G.1
  • 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: 2743-2749.
    • (2001) JAMA , vol.285 , pp. 2743-2749
    • Schiffmann, R.1    Kopp, J.B.2    Austin III, H.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.