Early HSCT corrects the skeleton in MPS.
Publication
, Journal Article
Kurtzberg, J
Published in: Blood
March 5, 2015
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]).
Duke Scholars
Published In
Blood
DOI
EISSN
1528-0020
Publication Date
March 5, 2015
Volume
125
Issue
10
Start / End Page
1518 / 1519
Location
United States
Related Subject Headings
- Mucopolysaccharidosis I
- Male
- Immunology
- Humans
- Female
- Bone Marrow Transplantation
- Bone Diseases, Developmental
- Animals
- 3213 Paediatrics
- 3201 Cardiovascular medicine and haematology
Citation
APA
Chicago
ICMJE
MLA
NLM
Kurtzberg, J. (2015). Early HSCT corrects the skeleton in MPS. Blood, 125(10), 1518–1519. https://doi.org/10.1182/blood-2014-11-606681
Kurtzberg, Joanne. “Early HSCT corrects the skeleton in MPS.” Blood 125, no. 10 (March 5, 2015): 1518–19. https://doi.org/10.1182/blood-2014-11-606681.
Kurtzberg J. Early HSCT corrects the skeleton in MPS. Blood. 2015 Mar 5;125(10):1518–9.
Kurtzberg, Joanne. “Early HSCT corrects the skeleton in MPS.” Blood, vol. 125, no. 10, Mar. 2015, pp. 1518–19. Pubmed, doi:10.1182/blood-2014-11-606681.
Kurtzberg J. Early HSCT corrects the skeleton in MPS. Blood. 2015 Mar 5;125(10):1518–1519.
Published In
Blood
DOI
EISSN
1528-0020
Publication Date
March 5, 2015
Volume
125
Issue
10
Start / End Page
1518 / 1519
Location
United States
Related Subject Headings
- Mucopolysaccharidosis I
- Male
- Immunology
- Humans
- Female
- Bone Marrow Transplantation
- Bone Diseases, Developmental
- Animals
- 3213 Paediatrics
- 3201 Cardiovascular medicine and haematology