Management of mucopolysaccharidosis type IH (Hurler’s syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution’s experience-Reference-Cited by-同舟云学术

Management of mucopolysaccharidosis type IH (Hurler’s syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution’s experience

Published:2012-06-21 Issue:2 Volume:36 Page:263-270
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Wiseman Daniel H.,Mercer Jean,Tylee Karen,Malaiya Nilima,Bonney Denise K.,Jones Simon A.,Wraith J Edmond,Wynn Robert F.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-012-9500-3

Reference39 articles.

1. Aldenhoven M, Boelens JJ, de Koning TJ (2008) The clinical outcome of Hurler syndrome after stem cell transplantation. Biol Blood Marrow Transplant 14(5):485–498

2. Appelbaum F, Strauchen JA, Graw RG et al (1976) Acute lethal carditis caused by high-dose combination chemotherapy. A unique clinical and pathological entity. Lancet 1(7950):58–62

3. Boelens JJ, Wynn RF, O’meara A et al (2007) Outcomes of hematopoietic stem cell transplantation for Hurler’s syndrome in Europe: a risk factor analysis for graft failure. Bone Marrow Transplant 40(3):225–233

4. Boelens JJ, Rocha V, Aldenhoven M et al (2009) Risk factor analysis of outcomes after unrelated cord blood transplantation in patients with hurler syndrome. Biol Blood Marrow Transplant 15(5):618–625

5. Braunlin EA, Stauffer NR, Peters CH et al (2003) Usefulness of bone marrow transplantation in the Hurler syndrome. Am J Cardiol 92(7):882–886

Cited by 32 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hematopoietic cell transplantation for Mucopolysaccharidosis I in the presence of decreased cardiac function;Molecular Genetics and Metabolism;2023-11

2. Natural history of cardiac findings in mucopolysaccharidosis type I: report from an international registry;Cardiology in the Young;2023-10-18

3. Evaluation of cardiac findings in mucopolysaccharidosis;The International Journal of Cardiovascular Imaging;2023-10-17

4. Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review;International Journal of Molecular Sciences;2023-05-11

5. Early Neonatal Cardiac Phenotype in Hurler Syndrome: Case Report and Literature Review;Genes;2022-07-22