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Volumn 32, Issue SUPPL. 1, 2009, Pages

Postmortem studies on a patient with mucopolysaccharidosis type I: Histopathological findings after one year of enzyme replacement therapy

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSAMINOGLYCAN; LEVO IDURONIDASE;

EID: 84881002836     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-009-1057-4     Document Type: Article
Times cited : (31)

References (9)
  • 1
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    • The Clinical Outcome of Hurler Syndrome after Stem Cell Transplantation
    • DOI 10.1016/j.bbmt.2008.01.009, PII S1083879108000529
    • Aldenhoven M, Boelens JJ, de Koning TJ (2008) The clinical outcome of Hurler syndrome after stem cell transplantation. Biol Blood Marrow Transplant 14: 485-498. doi:10.1016/j.bbmt.2008.01.009. (Pubitemid 351494741)
    • (2008) Biology of Blood and Marrow Transplantation , vol.14 , Issue.5 , pp. 485-498
    • Aldenhoven, M.1    Boelens, J.2    De Koning, T.J.3
  • 2
    • 33644816659 scopus 로고    scopus 로고
    • Cardiac functional and histopathologic findings in humans and mice with mucopolysaccharidosis type I: Implications for assessment of therapeutic interventions in Hurler syndrome
    • doi:10.1203/01.pdr.0000190579.24054.39.
    • Braunlin E, Mackey-Bojack S, Panoskaltsis-Mortari A, et al (2006) Cardiac functional and histopathologic findings in humans and mice with mucopolysaccharidosis type I: implications for assessment of therapeutic interventions in Hurler syndrome. Pediatr Res 59: 27-32. doi:10.1203/01.pdr. 0000190579.24054.39.
    • (2006) Pediatr Res , vol.59 , pp. 27-32
    • Braunlin, E.1    Mackey-Bojack, S.2    Panoskaltsis-Mortari, A.3
  • 3
    • 0033888320 scopus 로고    scopus 로고
    • Impaired elastogenesis in Hurler disease: Dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly
    • Hinek A, Wilson SE (2000) Impaired elastogenesis in Hurler disease: Dermatan sulfate accumulation linked to deficiency in elastin-binding protein and elastic fiber assembly. Am J Pathol 156: 925-938. (Pubitemid 30626951)
    • (2000) American Journal of Pathology , vol.156 , Issue.3 , pp. 925-938
    • Hinek, A.1    Wilson, S.E.2
  • 4
    • 31644436774 scopus 로고    scopus 로고
    • Mucopolysaccharidosis I under enzyme replacement therapy with laronidase - A mortality case with autopsy report
    • doi:10.1007/s10545-005-0211-x.
    • Lin HY, Lin SP, Chuang CK, et al (2005) Mucopolysaccharidosis I under enzyme replacement therapy with laronidase - a mortality case with autopsy report. J Inherit Metab Dis 28: 1146-1148. doi:10.1007/s10545-005-0211-x.
    • (2005) J Inherit Metab Dis , vol.28 , pp. 1146-1148
    • Lin, H.Y.1    Lin, S.P.2    Chuang, C.K.3
  • 9
    • 34447121276 scopus 로고    scopus 로고
    • Enzyme replacement therapy in patients who have mucopolysaccharidosis i and are younger than 5 years: Results of a multinational study of recombinant human α-L-iduronidase (laronidase)
    • DOI 10.1542/peds.2006-2156
    • Wraith JE, Beck M, Lane R, et al (2007) Enzyme replacement therapy in patients who have mucopolysaccharidosis I and are younger than 5 years: results of a multinational study of recombinant human α-L-Iduronidase (Laronidase). Pediatrics 120: e37-46. doi:10.1542/peds.2006-2156. (Pubitemid 47036214)
    • (2007) Pediatrics , vol.120 , Issue.1
    • Wraith, J.E.1    Beck, M.2    Lane, R.3    Van Der, P.A.4    Shapiro, E.5    Xue, Y.6    Kakkis, E.D.7    Guffon, N.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.