Therapies for the bone in mucopolysaccharidoses-Reference-Cited by-同舟云学术

Therapies for the bone in mucopolysaccharidoses

Published:2015-02 Issue:2 Volume:114 Page:94-109
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Tomatsu Shunji,Alméciga-Díaz Carlos J.,Montaño Adriana M.,Yabe Hiromasa,Tanaka Akemi,Dung Vu Chi,Giugliani Roberto,Kubaski Francyne,Mason Robert W.,Yasuda Eriko,Sawamoto Kazuki,Mackenzie William,Suzuki Yasuyuki,Orii Kenji E.,Barrera Luis A.,Sly William S.,Orii Tadao

Funder

Austrian MPS Society

National MPS Society

International Morquio Organization

National Institutes of Health

CNPq

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference139 articles.

1. The mucopolysaccharidoses;Neufeld,2001

2. Impairment of body growth in mucopolysaccharidoses;Tomatsu,2012

3. Growth charts for patients with Hunter syndrome;Patel;Mol. Genet. Metab. Rep.,2014

4. Mucopolysaccharidosis type IVA (Morquio A disease): clinical review and current treatment;Tomatsu;Curr. Pharm. Biotechnol.,2011

5. Characteristics of impulse oscillometry and thoracoabdominal motion in children with thoracic cage disorders;Rodriguez;Pediatr. Pulmonol.,2010

Cited by 81 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. Potential Targeting Mechanisms for Bone-Directed Therapies;International Journal of Molecular Sciences;2024-07-30

2. Molecular Mechanisms in Pathophysiology of Mucopolysaccharidosis and Prospects for Innovative Therapy;International Journal of Molecular Sciences;2024-01-17

3. Experimental Models of CNS Disorders Related to Lysosomal Storage Diseases;Journal of Evolutionary Biochemistry and Physiology;2023-11

4. Experimental Models of CNS Deficits in Lysosomal Storage Diseases;Российский физиологический журнал им И М Сеченова;2023-11-01

5. Current and Future Perspective in Hematopoietic Stem Progenitor Cell-gene Therapy for Inborn Errors of Metabolism;HemaSphere;2023-09-12