SCOPUS 정보 검색 플랫폼

Volumn , Issue , 2006, Pages 195-203

The mucopolysaccharidoses

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Indexed keywords

EID: 79953169083 PISSN: None EISSN: None Source Type: Book
DOI: 10.1007/3-540-28962-3_20 Document Type: Chapter

Times cited : (4)

References (11)

1
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- Alpha-l-iduronidase and enzyme replacement therapy for mucopolysaccharidosis i
- Brooks DA (2002) Alpha-l-iduronidase and enzyme replacement therapy for mucopolysaccharidosis I. Expert Opin Biol Ther 2:967-976
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- Brooks, D.A.¹

2
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- The use ofpartiallyhla-mismatched donors for allogeneic transplantation in patients with mucopolysaccharidosis-i
- FlemingDR,Henslee-Downey PJ, CiocciG,RomondEH,Marciniak E,MunnRK,ThompsonJS (1998) The use ofpartiallyHLA-mismatched donors for allogeneic transplantation in patients with mucopolysaccharidosis-I. Pediatr Transplant 2:299-304
- (1998) Pediatr Transplant , vol.2 , pp. 299-304
- Fleming, D.R.¹ Henslee-Downey, P.J.² Ciocci, G.³ Romond, E.H.⁴ Marciniak, E.⁵ Munn, R.K.⁶ Thompson, J.S.⁷

3
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- Enzyme-replacement therapy in mucopolysaccharidosis i
- Kakkis ED, Muenzer J, Tiller GE, et al. (2001) Enzyme-replacement therapy in mucopolysaccharidosis I. N Engl J Med 344:182-188
- (2001) N Engl J Med , vol.344 , pp. 182-188
- Kakkis, E.D.¹ Muenzer, J.² Tiller, G.E.³

4
- 0021683336
- Bone-marrow transplantation in the maroteaux-lamy syndrome (mucopolysaccharidosis type vi). Biochemical and clinical status 24 months after transplantation
- Krivit W, Pierpont ME, Ayaz K, et al. (1984) Bone-marrow transplantation in the Maroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Biochemical and clinical status 24 months after transplantation. N Engl J Med 311:1606-1611
- (1984) N Engl J Med , vol.311 , pp. 1606-1611
- Krivit, W.¹ Pierpont, M.E.² Ayaz, K.³

5
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- Umbilical cord blood transplantation formaroteaux-lamy syndrome (mucopolysaccharidosis type vi)
- LeeV, Li CK, ShingMM, ChikKW, LamCW, Tsang KS, Pong H,Huen KF, YuenPM(2000) Umbilical cord blood transplantation forMaroteaux-Lamy syndrome (mucopolysaccharidosis type VI). Bone Marrow Transplant 26:455-458
- (2000) Bone Marrow Transplant , vol.26 , pp. 455-458
- LeeV Li, C.K.¹ Shing, M.M.² Chik, K.W.³ Lam, C.W.⁴ Tsang, K.S.⁵ Pong, H.⁶ Huen, K.F.⁷ Yuen, P.M.⁸

6
- 0029795037
- Bone marrow transplantation in hunter syndrome
- McKinnis EJ, Sulzbacher S, Rutledge JC, Sanders J, Scott CR (1996) Bone marrow transplantation in Hunter syndrome. J Pediatr 129:145-148
- (1996) J Pediatr , vol.129 , pp. 145-148
- McKinnis, E.J.¹ Sulzbacher, S.² Rutledge, J.C.³ Sanders, J.⁴ Scott, C.R.⁵

7
- 0036984005
- Enzymereplacement therapy inmucopolysaccharidosis type ii (hunter syndrome): A preliminary report
- Muenzer J, Lamsa JC, Garcia A, Dacosta J, Garcia J,TrecoDA(2002). Enzymereplacement therapy inmucopolysaccharidosis type II (Hunter syndrome): a preliminary report.Acta Paediatr Suppl 91:98-99
- (2002) Acta Paediatr Suppl , vol.91 , pp. 98-99
- Muenzer, J.¹ Lamsa, J.C.² Garcia, A.³ Dacosta, J.⁴ Garcia, J.⁵ Treco, D.A.⁶

8
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- Outcome of unrelateddonor bonemarrow transplantation in 40 children with hurler syndrome
- Peters C, BalthazorM, Shapiro EG, et al. (1996)Outcome of unrelateddonor bonemarrow transplantation in 40 children with Hurler syndrome. Blood 87:4894-4902
- (1996) Blood , vol.87 , pp. 4894-4902
- Peters, C.¹ Balthazor, M.² Shapiro, E.G.³

9
- 0032055564
- Hurler syndrome: Ii. Outcome of hlagenotypically identical sibling and hla-haploidentical related donor bone marrow transplantation in fifty-four children. Storage disease collaborative study group
- Peters C, Shapiro EG, Anderson J, et al. (1998) Hurler syndrome: II. Outcome of HLAgenotypically identical sibling and HLA-haploidentical related donor bone marrow transplantation in fifty-four children. Storage Disease Collaborative Study Group. Blood 91:2601-2608
- (1998) Blood , vol.91 , pp. 2601-2608
- Peters, C.¹ Shapiro, E.G.² Anderson, J.³

10
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- Bone marrow transplantation in mucopolysaccharidosis type iiia: A comparison of an early treated patient with his untreated sibling
- Sivakumar P,Wraith JE (1999) Bone marrow transplantation in mucopolysaccharidosis type IIIA: a comparison of an early treated patient with his untreated sibling. J Inherit Metab Dis 22:849-850
- (1999) J Inherit Metab Dis , vol.22 , pp. 849-850
- Sivakumar, P.¹ Wraith, J.E.²

11
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- Enzyme replacement therapy for mucopolysaccharidosis i: A randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-l-iduronidase (laronidase)
- Wraith JE, Clarke LA, Beck M, Kolodny EH, Pastores GM, Muenzer J, Rapoport DM, Berger KI, Swiedler SJ, Kakkis ED, Braakman T, Chadbourne E, Walton-Bowen K, Cox GF (2004) Enzyme replacement therapy for mucopolysaccharidosis I: a randomized, double-blinded, placebo-controlled, multinational study of recombinant human alpha-l-iduronidase (laronidase). J Pediatr 144:581-588
- (2004) J Pediatr , vol.144 , pp. 581-588
- Wraith, J.E.¹ Clarke, L.A.² Beck, M.³ Kolodny, E.H.⁴ Pastores, G.M.⁵ Muenzer, J.⁶ Rapoport, D.M.⁷ Berger, K.I.⁸ Swiedler, S.J.⁹ Kakkis, E.D.¹⁰ Braakman, T.¹¹ Chadbourne, E.¹² Walton-Bowen, K.¹³ Cox, G.F.¹⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.