“Growth patterns in children with mucopolysaccharidosis type I-Hurler after hematopoietic stem cell transplantation: Comparison with untreated patients”-Reference-Cited by-同舟云学术

“Growth patterns in children with mucopolysaccharidosis type I-Hurler after hematopoietic stem cell transplantation: Comparison with untreated patients”

Published:2021-09 Issue: Volume:28 Page:100787
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Cattoni Alessandro,Chiaraluce Sofia,Gasperini Serena,Molinari Silvia,Biondi Andrea,Rovelli Attilio,Parini Rossella

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference31 articles.

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4. Growth, final height and endocrine sequelae in a UK population of patients with Hurler syndrome (MPS1H);Gardner;J. Inherit. Metab. Dis. [Internet],2011

5. Growth impairment in mucopolysaccharidoses;Melbouci;Mol. Genet. Metab.,2018

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1. Early skeletal outcomes after hematopoietic stem and progenitor cell gene therapy for Hurler syndrome;Science Translational Medicine;2024-05

2. Growth and Related Treatment Factors in Mucopolysaccharidoses Type I and II: A Systematic Review;Journal of Pediatrics Review;2023-10-01

3. Persistent bone and joint disease despite current treatments for mucopolysaccharidosis types I, II, and VI: Data from a 10‐year prospective study;Journal of Inherited Metabolic Disease;2023-03-06

4. MPSI Manifestations and Treatment Outcome: Skeletal Focus;International Journal of Molecular Sciences;2022-09-22

5. Proposal of an Algorithm to Early Detect Attenuated Type I Mucopolysaccharidosis (MPS Ia) among Children with Growth Abnormalities;Medicina;2022-01-08