Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome

Sunita Bijarnia, Peter Shaw, Anne Vimpani, Robert Smith, Verity Pacey, Helen O'Grady, John Christodoulou, David Sillence

Research output: Contribution to journalArticleResearchpeer-review

Abstract

We report the long-term follow-up of successful treatment of mucopolysaccharidosis type I H (MPS IH, Hurler syndrome) with combined enzyme replacement therapy and haematopoietic progenitor stem cell transplant.

LanguageEnglish
Pages469-472
Number of pages4
JournalJournal of paediatrics and child health
Volume45
Issue number7-8
DOIs
Publication statusPublished - Jul 2009
Externally publishedYes

Fingerprint

Mucopolysaccharidosis I
Hematopoietic Stem Cell Transplantation
Hematopoietic Stem Cells
Enzyme Replacement Therapy
Enzymes
Transplants
Therapeutics

Cite this

Bijarnia, Sunita ; Shaw, Peter ; Vimpani, Anne ; Smith, Robert ; Pacey, Verity ; O'Grady, Helen ; Christodoulou, John ; Sillence, David. / Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome. In: Journal of paediatrics and child health. 2009 ; Vol. 45, No. 7-8. pp. 469-472.
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Bijarnia, S, Shaw, P, Vimpani, A, Smith, R, Pacey, V, O'Grady, H, Christodoulou, J & Sillence, D 2009, 'Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome', Journal of paediatrics and child health, vol. 45, no. 7-8, pp. 469-472. https://doi.org/10.1111/j.1440-1754.2009.01537.x

Combined enzyme replacement and haematopoietic stem cell transplantation in Hurler syndrome. / Bijarnia, Sunita; Shaw, Peter; Vimpani, Anne; Smith, Robert; Pacey, Verity; O'Grady, Helen; Christodoulou, John; Sillence, David.

In: Journal of paediatrics and child health, Vol. 45, No. 7-8, 07.2009, p. 469-472.

Research output: Contribution to journalArticleResearchpeer-review

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AU - Bijarnia, Sunita

AU - Shaw, Peter

AU - Vimpani, Anne

AU - Smith, Robert

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AU - O'Grady, Helen

AU - Christodoulou, John

AU - Sillence, David

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