Mucopolysaccharidosis type II (Hunter syndrome): Clinical and biochemical aspects of the disease and approaches to its diagnosis and treatment-Reference-Cited by-同舟云学术

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Mucopolysaccharidosis type II (Hunter syndrome): Clinical and biochemical aspects of the disease and approaches to its diagnosis and treatment

Published:2020 Issue: Volume: Page:71-117
ISSN:0065-2318
Container-title:Advances in Carbohydrate Chemistry and Biochemistry
language:
Short-container-title:

Author:

Mohamed Shifaza,He Qi Qi,Singh Arti A.,Ferro Vito

Funder

Australian Research Council

University of Queensland

National MPS Society

Publisher

Elsevier

Reference196 articles.

1. Lysosomal Storage Diseases—The Horizon Expands;Boustany;Nat. Rev. Neurol.,2013

2. Lysosomal Storage Disorders;Vellodi;Br. J. Haematol.,2005

3. Lysosomal Disorders: From Storage to Cellular Damage;Ballabio;Biochim. Biophys. Acta,2009

4. Classification of Lysosomal Storage Diseases;Winchester,2012

5. Emerging Drugs for Lysosomal Storage Diseases;Beck;Expert Opin. Emerg. Drugs,2010

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1. Sialorrhea in children with mucopolysaccharidosis type II (a review of several clinical cases);L.O. Badalyan Neurological Journal;2024-07-31

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3. Foramen magnum stenosis in patients with mucopolysaccharidoses: diagnosis and surgical treatment. Review of literature;Russian Journal for Personalized Medicine;2024-06-11

4. On the Mechanism of the Lysosomal Enzyme Iduronate‐2‐sulfatase. A Multiscale Approach;ChemCatChem;2024-04-26

5. The Impact of Pabinafusp Alfa on the Disease Burden in Hunter's Syndrome: Patient-Reported Outcomes;Journal of Pediatric Neurology;2024-03-01

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