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Pediatric Pulmonology, ISSN 8755-6863, 03/2014, Volume 49, Issue 3, pp. 277 - 284
Background The mucopolysaccharidoses (MPS) comprise a group of inherited lysosomal storage disorders characterized by deficiencies in enzymes catalyzing the... 
glycosaminoglycans | pulmonary function | enzyme replacement therapy | spirometry | mucopolysaccharidoses | MORTALITY | LARONIDASE | EQUATIONS | CHINESE CHILDREN | HONG-KONG | REFERENCE VALUES | RESPIRATORY SYSTEM | PEDIATRICS | Spirometry | Age Factors | Mucopolysaccharidosis IV - complications | Humans | Mucopolysaccharidosis I - physiopathology | Mucopolysaccharidosis VI - complications | Male | Mucopolysaccharidosis III - drug therapy | Lung Diseases - etiology | Forced Expiratory Volume | Young Adult | Mucopolysaccharidosis II - physiopathology | Adult | Female | Mucopolysaccharidoses - complications | Mucopolysaccharidosis VI - drug therapy | Child | Mucopolysaccharidosis VI - physiopathology | Mucopolysaccharidoses - drug therapy | Severity of Illness Index | Mucopolysaccharidoses - physiopathology | Mucopolysaccharidosis III - physiopathology | Treatment Outcome | Lung - physiopathology | Mucopolysaccharidosis IV - drug therapy | Disease Progression | Mucopolysaccharidosis I - complications | Lung Diseases, Obstructive - physiopathology | Mucopolysaccharidosis III - complications | Enzyme Replacement Therapy - methods | Mucopolysaccharidosis II - complications | Mucopolysaccharidosis IV - physiopathology | Mucopolysaccharidosis II - drug therapy | Mucopolysaccharidosis I - drug therapy | Vital Capacity - physiology | Adolescent | Lung Diseases, Obstructive - etiology | Lung Diseases - physiopathology | Respiratory Function Tests | Peak Expiratory Flow Rate | Maximal Midexpiratory Flow Rate | Enzymes | Respiratory tract diseases | Care and treatment | Mucopolysaccharidosis | Glycosaminoglycans | Chemical properties
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 09/2018, Volume 125, Issue 1-2, pp. 44 - 52
To explore the correlation between glycosaminoglycan (GAG) levels and mucopolysaccharidosis (MPS) type, we have evaluated the GAG levels in blood of MPS II,... 
Heparan sulfate | LC/MS | Hyaluronan | Glycosaminoglycans | Dermatan sulfate | Keratan sulfate | Mucopolysaccharidoses | Chondroitin sulfate | MEDICINE, RESEARCH & EXPERIMENTAL | TANDEM MASS-SPECTROMETRY | HUMAN SERUM | PERFORMANCE LIQUID-CHROMATOGRAPHY | THIN-LAYER-CHROMATOGRAPHY | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | SULFATE-DERIVED DISACCHARIDES | HEPARAN-SULFATE | CHONDROITIN/DERMATAN SULFATE | ACIDIC GLYCOSAMINOGLYCANS | Mucopolysaccharidoses - urine | Glycosaminoglycans - blood | Biomarkers - urine | Mucopolysaccharidosis III - urine | Humans | Mucopolysaccharidosis III - pathology | Child, Preschool | Keratan Sulfate - blood | Male | Heparitin Sulfate - urine | Mucopolysaccharidosis II - urine | Dermatan Sulfate - urine | Mucopolysaccharidoses - pathology | Mucopolysaccharidoses - classification | Young Adult | Glycosaminoglycans - isolation & purification | Mucopolysaccharidosis II - pathology | Tandem Mass Spectrometry | Keratan Sulfate - urine | Mucopolysaccharidosis IV - pathology | Adult | Female | Child | Glycosaminoglycans - urine | Mucopolysaccharidosis IV - urine | Mucopolysaccharidosis III - blood | Mucopolysaccharidoses - blood | Mucopolysaccharidosis VI - urine | Dermatan Sulfate - blood | Mucopolysaccharidosis VI - pathology | Biomarkers - blood | Mucopolysaccharidosis II - blood | Heparitin Sulfate - blood | Adolescent | Mucopolysaccharidosis VI - blood | Mucopolysaccharidosis IV - blood | Mucopolysaccharidosis | Sulfates | Mass spectrometry | Analysis | glycosaminoglycans | dermatan sulfate | heparan sulfate | mucopolysaccharidoses | chondroitin sulfate | hyaluronan | keratan sulfate
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 12/2016, Volume 17, Issue 12, pp. 2004 - 2004
Journal Article
Osteoarthritis and Cartilage, ISSN 1063-4584, 2013, Volume 21, Issue 12, pp. 1813 - 1823
Summary Background Mucopolysaccharidoses (MPSs) are rare genetic diseases caused by a deficient activity of one of the lysosomal enzymes involved in the... 
Rheumatology | Osteoimmunology | Dysostosis multiplex | Mucopolysaccharidosis | Metabolic inflammation | anti-TNF | ISOFLAVONE EXTRACT | STORAGE DISEASE | GENISTEIN-MEDIATED INHIBITION | BONE-MARROW-TRANSPLANTATION | HURLER-DISEASE | JOINT DISEASE | RHEUMATOLOGY | GLYCOSAMINOGLYCAN SYNTHESIS | FELINE MODEL | GROWTH-PLATE | ORTHOPEDICS | ENZYME REPLACEMENT THERAPY | Synovitis - metabolism | Mucopolysaccharidosis VI - immunology | Mucopolysaccharidosis VII - metabolism | Mucopolysaccharidoses - metabolism | Humans | Mucopolysaccharidosis VI - complications | Bone Diseases - metabolism | Mucopolysaccharidoses - immunology | Bone Diseases - etiology | Mucopolysaccharidosis II - metabolism | Cartilage, Articular - metabolism | Dysostoses - metabolism | Synovitis - etiology | Synovitis - immunology | Mucopolysaccharidoses - complications | Joint Diseases - immunology | Mucopolysaccharidosis I - metabolism | Glycosaminoglycans - metabolism | Joint Diseases - metabolism | Glycosaminoglycans - immunology | Dysostoses - immunology | Bone Diseases - immunology | Mucopolysaccharidosis I - complications | Mucopolysaccharidosis II - complications | Mucopolysaccharidosis I - immunology | Joint Diseases - etiology | Mucopolysaccharidosis VI - metabolism | Mucopolysaccharidosis VII - immunology | Mucopolysaccharidosis II - immunology | Mucopolysaccharidosis VII - complications | Cartilage, Articular - immunology | Dysostoses - etiology | Enzymes | Medical colleges | Inflammation | Glycosaminoglycans | Medical genetics
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 12/2012, Volume 107, Issue 4, pp. 705 - 710
Journal Article
PLoS ONE, ISSN 1932-6203, 05/2016, Volume 11, Issue 5, p. e0156452
Lysosomal Storage Disorders (LSDs) are a group of metabolic syndromes, each one due to the deficit of one lysosomal enzyme. Many LSDs affect most of the organ... 
HUNTER-SYNDROME | TRANSPORT | THERAPY | DISEASES | DRUG-DELIVERY | INFLAMMATION | CONVECTION | MULTIDISCIPLINARY SCIENCES | BARRIER | CENTRAL-NERVOUS-SYSTEM | MOUSE MODELS | Albumins - chemistry | Fluorescein-5-isothiocyanate - pharmacokinetics | Nanoparticles - chemistry | Polylactic Acid-Polyglycolic Acid Copolymer | Polyglycolic Acid - pharmacology | Drug Carriers - chemistry | Lactic Acid - pharmacokinetics | Mucopolysaccharidosis II - pathology | Fluorescein-5-isothiocyanate - chemistry | Mucopolysaccharidosis II - metabolism | Nanoparticles - therapeutic use | Mucopolysaccharidosis II - genetics | Lactic Acid - pharmacology | Disease Models, Animal | Mucopolysaccharidosis I - metabolism | Fluorescein-5-isothiocyanate - pharmacology | Lactic Acid - chemistry | Mucopolysaccharidosis I - pathology | Drug Carriers - pharmacology | Blood-Brain Barrier - metabolism | Mice, Knockout | Enzyme Replacement Therapy - methods | Albumins - pharmacokinetics | Albumins - pharmacology | Animals | Polyglycolic Acid - pharmacokinetics | Mucopolysaccharidosis II - drug therapy | Mucopolysaccharidosis I - drug therapy | Polyglycolic Acid - chemistry | Mucopolysaccharidosis I - genetics | Drug Carriers - pharmacokinetics | Mice | Metabolism, Inborn errors of | Nanoparticles | Enzymes | Blood-brain barrier | Analysis | Albumin | Research | Health aspects | Therapy | Pediatrics | Animal models | Drug delivery systems | Disease | Biodegradability | Central nervous system | Disorders | Lysosomal storage diseases | Nervous system | Mucopolysaccharidosis | Neurosurgery | Molecular weight | Polylactide-co-glycolide | Biomedical materials | Low molecular weights | Rodents | Biocompatibility | Life sciences | Biodegradation | Phenotypes | Brain research | Storage | Acids | Womens health | Neurological complications | Metabolic disorders | Apoptosis
Journal Article
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 Article
Pediatric Anesthesia, ISSN 1155-5645, 08/2012, Volume 22, Issue 8, pp. 737 - 744
Journal Article
Cardiovascular Pathology, ISSN 1054-8807, 2014, Volume 23, Issue 3, pp. 145 - 151
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2014, Volume 111, Issue 2, pp. 128 - 132
Journal Article