Early HSCT corrects the skeleton in MPS.
| dc.contributor.author | Kurtzberg, Joanne | |
| dc.date.accessioned | 2022-03-23T19:06:14Z | |
| dc.date.available | 2022-03-23T19:06:14Z | |
| dc.date.issued | 2015-03 | |
| dc.date.updated | 2022-03-23T19:06:13Z | |
| dc.description.abstract | In this issue of Blood, Pievani et al have identified a potential solution to the remaining barrier to the success of hematopoietic stem cell transplantation (HSCT) in children with severe phenotype Hurler syndrome (mucopolysaccharidosis type I [MPS I]). | |
| dc.identifier | S0006-4971(20)35184-3 | |
| dc.identifier.issn | 0006-4971 | |
| dc.identifier.issn | 1528-0020 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | American Society of Hematology | |
| dc.relation.ispartof | Blood | |
| dc.relation.isversionof | 10.1182/blood-2014-11-606681 | |
| dc.subject | Animals | |
| dc.subject | Humans | |
| dc.subject | Bone Diseases, Developmental | |
| dc.subject | Mucopolysaccharidosis I | |
| dc.subject | Bone Marrow Transplantation | |
| dc.subject | Female | |
| dc.subject | Male | |
| dc.title | Early HSCT corrects the skeleton in MPS. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Kurtzberg, Joanne|0000-0002-3370-0703 | |
| pubs.begin-page | 1518 | |
| pubs.end-page | 1519 | |
| pubs.issue | 10 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Pathology | |
| pubs.organisational-group | Pediatrics | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | Institutes and Provost's Academic Units | |
| pubs.organisational-group | Initiatives | |
| pubs.organisational-group | Duke Innovation & Entrepreneurship | |
| pubs.organisational-group | Pediatrics, Transplant and Cellular Therapy | |
| pubs.publication-status | Published | |
| pubs.volume | 125 |
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