Disease-Specific Markers for the Mucopolysaccharidoses-Reference-Cited by-同舟云学术

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Disease-Specific Markers for the Mucopolysaccharidoses

Published:2004-11 Issue:5 Volume:56 Page:733-738
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Fuller Maria,Rozaklis Tina,Ramsay Steven L,Hopwood John J,Meikle Peter J

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology and Child Health

Reference13 articles.

1. Prevalence of Lysosomal Storage Disorders

2. Enzyme-Replacement Therapy in Mucopolysaccharidosis I

4. Long-term outcome of Hurler syndrome following bone marrow transplantation

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2. Secondary deficiency of neuraminidase 1 contributes to CNS pathology in neurological mucopolysaccharidoses via hypersialylation of brain glycoproteins;2024-04-27

3. Ultra-Performance Liquid Chromatography–Tandem Mass Spectrometry Analysis of Urinary Oligosaccharides and Glycoamino Acids for the Diagnosis of Mucopolysaccharidosis and Glycoproteinosis;Clinical Chemistry;2024-04-10

4. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024

5. Endogenous, non-reducing end glycosaminoglycan biomarkers are superior to internal disaccharide glycosaminoglycan biomarkers for newborn screening of mucopolysaccharidoses and GM1 gangliosidosis;Molecular Genetics and Metabolism;2023-09

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