메뉴 건너뛰기




Volumn 7, Issue , 2013, Pages 31-37

Quality of life of brazilian patients with gaucher disease and fabry disease

Author keywords

Enzyme replacement therapy; Fabry disease; Gauche disease; Mental component score; Physical component score

Indexed keywords


EID: 84886851749     PISSN: 21928304     EISSN: 21928312     Source Type: Book Series    
DOI: 10.1007/8904_2012_136     Document Type: Chapter
Times cited : (20)

References (24)
  • 1
    • 85060723092 scopus 로고    scopus 로고
    • Brazilian-Portuguese version of the SF-36. A reliable and valid quality of life outcome measure
    • Ciconelli RM, Ferraz MB, Santos W, Meinão I, Quaresma MR (1997) Brazilian-Portuguese version of the SF-36. A reliable and valid quality of life outcome measure. Rev Bras Reumatol 39:50
    • (1997) Rev Bras Reumatol , vol.39 , pp. 50
    • Ciconelli, R.M.1    Ferraz, M.B.2    Santos, W.3    Meinão, I.4    Quaresma, M.R.5
  • 2
    • 0031877439 scopus 로고    scopus 로고
    • The health-related quality of life of adults with Gaucher’s disease receiving enzyme replacement therapy: Results from a retrospective study
    • Damiano AM, Pastores GM, Ware JE (1998) The health-related quality of life of adults with Gaucher’s disease receiving enzyme replacement therapy: results from a retrospective study. Qual Life Res 7:373–386
    • (1998) Qual Life Res , vol.7 , pp. 373-386
    • Damiano, A.M.1    Pastores, G.M.2    Ware, J.E.3
  • 3
    • 0028962656 scopus 로고
    • Lysosomal storage diseases
    • Gieselmann V (1995) Lysosomal storage diseases. Biochim Biophys Acta 1270:103–136
    • (1995) Biochim Biophys Acta , vol.1270 , pp. 103-136
    • Gieselmann, V.1
  • 4
    • 0033826442 scopus 로고    scopus 로고
    • Report of the Spanish Gaucher’s Disease Registry: Clinical and genetic characteristics
    • Giraldo P, Pocoví M, Pérez-Calvo J, Rubio-Félix D, Giralt M (2000) Report of the Spanish Gaucher’s Disease Registry: clinical and genetic characteristics. Haematologica 85:792–799
    • (2000) Haematologica , vol.85 , pp. 792-799
    • Giraldo, P.1    Pocoví, M.2    Pérez-Calvo, J.3    Rubio-Félix, D.4    Giralt, M.5
  • 7
    • 0033947788 scopus 로고    scopus 로고
    • Determining minimally important changes in generic and disease-specific health-related quality of life questionnaires in clinical trials of rheumatoid arthritis
    • Kosinski M, Zhao SZ, Dedhiya S, Osterhaus JT, Ware JE Jr (2000) Determining minimally important changes in generic and disease-specific health-related quality of life questionnaires in clinical trials of rheumatoid arthritis. Arthritis Rheum 43:1478–1487
    • (2000) Arthritis Rheum , vol.43 , pp. 1478-1487
    • Kosinski, M.1    Zhao, S.Z.2    Dedhiya, S.3    Osterhaus, J.T.4    Ware, J.E.5
  • 10
    • 0027569430 scopus 로고
    • The MOS 36-Item Short-Form Health Survey (SF-36): II. Psychometric and clinical tests of validity in measuring physical and mental health constructs
    • McHorney CA, Ware JE Jr, Raczek AE (1993) The MOS 36-Item Short-Form Health Survey (SF-36): II. Psychometric and clinical tests of validity in measuring physical and mental health constructs. Med Care 31:247–263
    • (1993) Med Care , vol.31 , pp. 247-263
    • McHorney, C.A.1    Ware, J.E.2    Raczek, A.E.3
  • 13
    • 36949037488 scopus 로고    scopus 로고
    • Quality of life and spiritual-religious coping relations
    • Panzini RG, Bandeira DR (2005) Quality of life and spiritual-religious coping relations. Qual Life Res 14:2106–2107
    • (2005) Qual Life Res , vol.14 , pp. 2106-2107
    • Panzini, R.G.1    Bandeira, D.R.2
  • 15
    • 77952713435 scopus 로고    scopus 로고
    • Expression of the disease on female carriers of X-linked lysosomal disorders: A brief review
    • Pinto LL, Vieira TA, Giugliani R, Schwartz IV (2010) Expression of the disease on female carriers of X-linked lysosomal disorders: a brief review. Orphanet J Rare Dis 5:14
    • (2010) Orphanet J Rare Dis , vol.5 , pp. 14
    • Pinto, L.L.1    Vieira, T.A.2    Giugliani, R.3    Schwartz, I.V.4
  • 16
    • 0032780351 scopus 로고    scopus 로고
    • The frequency of lysosomal storage diseases in The Netherlands
    • Poorthuis BJ, Wevers RA, Kleijer WJ et al (1999) The frequency of lysosomal storage diseases in The Netherlands. Hum Genet 105:151–156
    • (1999) Hum Genet , vol.105 , pp. 151-156
    • Poorthuis, B.J.1    Wevers, R.A.2    Kleijer, W.J.3
  • 19
    • 0009686664 scopus 로고
    • Development of the WHOQOL: Rationale and current status
    • The WHOQOL Group (1994) Development of the WHOQOL: rationale and current status. Int J Ment Health 23:24–56
    • (1994) Int J Ment Health , vol.23 , pp. 24-56
  • 22
    • 34249662242 scopus 로고    scopus 로고
    • Imiglucerase (Cerezyme) improves quality of life in patients with skeletal manifestations of Gaucher disease
    • Weinreb N, Barranger J, Packman S et al (2007) Imiglucerase (Cerezyme) improves quality of life in patients with skeletal manifestations of Gaucher disease. Clin Genet 71:576–588
    • (2007) Clin Genet , vol.71 , pp. 576-588
    • Weinreb, N.1    Barranger, J.2    Packman, S.3
  • 23
    • 0036303882 scopus 로고    scopus 로고
    • Lysosomal disorders
    • Wraith JE (2002) Lysosomal disorders. Semin Neonatol 7:75–83
    • (2002) Semin Neonatol , vol.7 , pp. 75-83
    • Wraith, J.E.1
  • 24
    • 0026465017 scopus 로고
    • Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patients
    • Zimran A, Kay A, Gelbart T, Garver P, Thurston D, Saven A, Beutler E (1992) Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patients. Medicine 71:337–53
    • (1992) Medicine , vol.71 , pp. 337-353
    • Zimran, A.1    Kay, A.2    Gelbart, T.3    Garver, P.4    Thurston, D.5    Saven, A.6    Beutler, E.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.