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PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, p. e35787
Mucopolysaccharide diseases (MPS) are caused by deficiency of glycosaminoglycan (GAG) degrading enzymes, leading to GAG accumulation. Neurodegenerative MPS... 
TARGETED DISRUPTION | MICROGLIAL ACTIVATION | SANFILIPPO-SYNDROME | DISEASE | BIOLOGY | SYNDROME TYPE-B | MICE | HEPARAN-SULFATE PROTEOGLYCANS | LYSOSOMAL STORAGE DISORDERS | ALPHA-L-IDURONIDASE | BRAIN | Immunohistochemistry | Neurons - pathology | Mucopolysaccharidosis III - pathology | Male | Parietal Lobe - metabolism | Heparitin Sulfate - metabolism | Somatosensory Cortex - pathology | Lysosomes - metabolism | Homer Scaffolding Proteins | Mucopolysaccharidosis III - metabolism | Female | Lysosomes - pathology | Neurons - metabolism | G(M2) Ganglioside - biosynthesis | Disease Models, Animal | Glycosaminoglycans - biosynthesis | Mucopolysaccharidosis I - metabolism | Mucopolysaccharidosis I - pathology | Carrier Proteins - biosynthesis | Disease Progression | Parietal Lobe - pathology | Animals | Vesicle-Associated Membrane Protein 2 - biosynthesis | Mice | Cytokines - biosynthesis | Somatosensory Cortex - metabolism | Enzymes | Brain | Neurons | Analysis | Models | Gangliosides | Animal models | Gangliosidosis | Transplants & implants | Disease | Neuropathology | Genes | Cognitive ability | Ganglioside GM2 | Schizophrenia | Cortex (somatosensory) | Mucopolysaccharidosis | Cortex (motor) | Proteins | Blood-brain barrier | Neurodegeneration | Cortex (parietal) | Rodents | Fibroblasts | Bone marrow | Growth factors | Genotypes | Heparan sulfate | Synaptophysin | Inflammation | Electron microscopy | Sulfation | Membrane proteins | Pathology | Axons | Gliosis | Hospitals | Transmission electron microscopy | Acids | Life span | Cell number | Stem cells | Monocyte chemoattractant protein 1
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2018, Volume 13, Issue 3, p. e0193694
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2018, Volume 123, Issue 2, pp. S24 - S25
Journal Article
SCIENTIFIC REPORTS, ISSN 2045-2322, 10/2019, Volume 9, Issue 1, pp. 1 - 6
Allogeneic hematopoietic cell transplantation (HCT) benefits children with Hurler syndrome (MPS-IH). However, survivors remain burdened by substantial MPS-IH... 
EFFICACY | STEM-CELL TRANSPLANTATION | ENZYME REPLACEMENT THERAPY | MULTIDISCIPLINARY SCIENCES | Glycosaminoglycans | Intravenous administration | Transplants & implants | Clinical trials | Transplantation | Children | Hemopoiesis
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S59 - S60
Journal Article
PloS one, ISSN 1932-6203, 2018, Volume 13, Issue 9, p. e0203216
Introduction Mucopolysaccharide diseases are a group of lysosomal storage disorders caused by deficiencies of hydrolase enzymes, leading to pathological... 
HURLER-SYNDROME | MANAGEMENT | COLLAGEN | LARONIDASE | MULTIDISCIPLINARY SCIENCES | PROTEOGLYCAN DEPOSITION | ENDOTHELIAL-CELLS | HEMATOPOIETIC STEM-CELL | BACTERIAL SUPERINFECTION | HEPARAN-SULFATE | ALPHA-L-IDURONIDASE | Tumor Necrosis Factor-alpha - metabolism | Adenoids - pathology | Mucopolysaccharidoses - metabolism | Humans | Tumor Necrosis Factor-alpha - genetics | Child, Preschool | Extracellular Matrix - metabolism | Infant | Interleukin-1alpha - metabolism | Male | Mucopolysaccharidosis III - drug therapy | Mucopolysaccharidoses - pathology | Palatine Tonsil - metabolism | Inflammation Mediators - metabolism | Female | Interleukin-1alpha - genetics | Mucopolysaccharidosis VI - drug therapy | Child | Interleukin-6 - metabolism | Mucopolysaccharidoses - drug therapy | Interleukin-6 - genetics | Adenoids - metabolism | Mucopolysaccharidosis IV - drug therapy | Enzyme Replacement Therapy - methods | Palatine Tonsil - pathology | Mucopolysaccharidosis I - drug therapy | Immunohistochemistry | Enzymes | Usage | Care and treatment | Mucopolysaccharidosis | Genetic aspects | Health aspects | Therapy | Glycosaminoglycans | Disease | Otolaryngology | Lysosomal storage diseases | Biology | Remodeling | Accumulation | Interleukin 6 | Genotype & phenotype | Airway management | Alterations | Laminin | Extracellular matrix | Respiratory tract diseases | Collagen (type IV) | Heparan sulfate | Phenotypes | Biochemical analysis | Cytokines | Hydrolase | Inflammation | Tumor necrosis factor-α | Metabolism | Patients | Substrates | Medicine | Sleep | Hospitals | Collagen | Stem cells | Sampling methods
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 01/2017, Volume 120, Issue 1-2, pp. S56 - S57
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 12, p. e14192
Journal Article