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Archives de pediatrie, ISSN 0929-693X, 06/2014, Volume 21, p. S14-S21
Les mucopolysaccharidoses (MPS) sont des maladies de surcharge lysosomale multisystemiques et progressives dues au defaut de catabolisme et a l'accumulation... 
Mucopolysaccharidosis
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 05/2008, Volume 53, Issue 5, p. 467
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S120 - S120
Journal Article
Italian journal of pediatrics, ISSN 1824-7288, 06/2019, Volume 45, Issue 1, pp. 71 - 1
The original article contains an unintended omission of a statement of competing interests. As such, the authors would like to declare the following complete... 
Medical screening | Mucopolysaccharidosis
Journal Article
Case Report - Hurler syndrome with a tuft of hair, 12/2006
A 2-year-old girl presented with coarse, thick hairy skin all over the body, a tuft of hair in the parietal region, coarse facial features and a prominent... 
Bone marrow, Hurler syndrome, Mucopolysaccharidosis (MPS) - type I, Transplantation
Journal
R & D Focus Drug News, ISSN 1350-1135, 10/2019
Journal Article
Molecular genetics and metabolism, ISSN 1096-7192, 2017, Volume 120, Issue 1-2, pp. 101 - 110
Mucopolysaccharidosis type I (MPS I) is due to deficiency of α-L-iduronidase (IDUA) and subsequent storage of undegraded glycosaminoglycans (GAG). The severe... 
proteomics | mucopolysaccharidosis | 2D-PAGE
Journal Article
Paediatria Croatica, ISSN 1330-1403, 04/2015, Volume 59, Issue 2, pp. 99 - 105
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 4994 - 3
A correction to this article has been published and is linked from the HTML and PDF versions of this paper. The error has not been fixed in the paper. 
Mucopolysaccharidosis
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S91 - S91
Journal Article
Proceedings of the National Academy of Sciences of the United States, ISSN 0027-8424, 10/2014, Volume 111, Issue 41, p. 14870
Mucopolysaccharidosis type IIIB (MPS IIIB, Sanfilippo syndrome type B) is a lysosomal storage disease characterized by profound intellectual disability,... 
Care and treatment | Causes of | Mucopolysaccharidosis
Journal Article
American Journal of Clinical Pathology, ISSN 0002-9173, 10/2015, Volume 144, Issue suppl_2, pp. A022 - A022
Mucopolysaccharidosis type IIIA (MPS-IIIA, Sanfilippo syndrome) is a lysosomal storage disease caused by deficiency of N-sulfoglucosamine sulfohydrolase (SGSH)... 
Heparan sulfate | Mucopolysaccharidosis | Mutation | Autopsy
Journal Article
Travmatologiâ i Ortopediâ Rossii, ISSN 2311-2905, 07/2018, Volume 24, Issue 2, pp. 127 - 137
A multidisciplinary approach to treatment of patients with mucopolysaccharidosis allows to achieve good results. However, progressive spinal canal stenosis at... 
stenosis | Mucopolysaccharidosis
Journal Article
European Journal of Paediatric Neurology, ISSN 1090-3798, 2015, Volume 19, pp. S117 - S117
Objective Hunter syndrome (mucopolysaccharidosis type II, MPS II, OMIM 309900) is a lysosomal storage disease with progressive multisystem manifestations... 
Pediatrics | Neurology | Surveys | Mucopolysaccharidosis
Journal Article
R & D Focus Drug News, ISSN 1350-1135, 06/2018
Journal Article
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