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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]).

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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