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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 09/2019, Volume 20, Issue 17, p. 4139
Mucopolysaccharidosis IVA (MPS IVA) is caused by a deficiency of the lysosomal enzyme N-acetylgalactosamine-6-sulfate sulfatase (GALNS). Conventional enzyme... 
MPS IVA | MORQUIO | GLYCOSAMINOGLYCANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | thermostable keratanase | HUMAN SERUM | CHEMISTRY, MULTIDISCIPLINARY | skeletal dysplasia | CARTILAGE | GALNS | PLASMA | keratan sulfate | REPLACEMENT THERAPY | HEPARAN-SULFATE | BONE | STEM-CELL TRANSPLANTATION
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S143 - S144
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S144 - S144
Journal Article
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2018, Volume 123, Issue 2, pp. S140 - S140
Journal Article
Drug Design, Development and Therapy, ISSN 1177-8881, 04/2015, Volume 9, pp. 1937 - 1953
Patients with mucopolysaccharidosis IVA (MPS IVA) can present with systemic skeletal dysplasia, leading to a need for multiple orthopedic surgical procedures,... 
Mucopolysaccharidosis IVA | Skeletal dysplasia | HSCT | ERT | Keratan sulfate | HURLER-SYNDROME | CHEMISTRY, MEDICINAL | mucopolysaccharidosis IVA | BONE-MARROW-TRANSPLANTATION | DRUG-DELIVERY SYSTEM | MUCOPOLYSACCHARIDOSIS TYPE-IVA | LYSOSOMAL STORAGE DISORDERS | II HUNTER-SYNDROME | skeletal dysplasia | MAROTEAUX-LAMY-SYNDROME | keratan sulfate | RECOMBINANT N-ACETYLGALACTOSAMINE-6-SULFATE SULFATASE | TERM-FOLLOW-UP | PHARMACOLOGY & PHARMACY | Hematopoietic Stem Cell Transplantation | Enzyme Replacement Therapy | Mucopolysaccharidosis IV - therapy | Humans | Enzymes | Care and treatment | Patient outcomes | Mucopolysaccharidosis | Transplantation | Health aspects | Hematopoietic stem cells | Methods | Heart | Therapy | Pediatrics | N-Acetylgalactosamine | Respiratory function | Deformation | Syngeneic grafts | Genotype & phenotype | Microorganisms | Apnea | Wheelchairs | Bone marrow | Bone dysplasia | Biocompatibility | Trochanter | Activities of daily living | Orthoses | Knee (anatomy) | Patients | Heart valves | Quality of life | Radiography | Pathology | Storage | Radiographs | Stem cells | Chondrocytes | Biomarkers | Scientific imaging | Mass spectrometry | Knee | Yeast | Transplants & implants | Medical services | Bone marrow transplantation | Stem cell transplantation | Pichia pastoris | Sulfates | Sleep disorders | Biomedical materials | Reduction | Skeleton | Lesions | Recombinant | Bone lesions | Medical screening | Chromatography | Hip | Hemopoiesis | Ankle | Lungs | Coronary vessels | Climb | Bone mineral density
Journal Article
JOURNAL OF HUMAN GENETICS, ISSN 1434-5161, 11/2019, Volume 64, Issue 11, pp. 1153 - 1171
Mucopolysaccharidoses (MPS) are a group of lysosomal storage disorders, which lack an enzyme corresponding to the specific type of MPS. Enzyme replacement... 
ATTENUATES DISEASE PROGRESSION | BONE-MARROW-TRANSPLANTATION | HUMAN ARYLSULFATASE-B | DRUG-DELIVERY SYSTEM | RECEPTOR ANTIBODY | GENETICS & HEREDITY | STEM-CELL TRANSPLANTATION | 2 JAPANESE SIBLINGS | BLOOD-BRAIN-BARRIER | ALPHA-N-ACETYLGLUCOSAMINIDASE | HUNTER-SYNDROME DATA
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 09/2019, Volume 10, Issue 1, pp. 4045 - 14
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S144 - S145
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2016, Volume 117, Issue 2, pp. S113 - S113
Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2018, Volume 123, Issue 2, pp. S140 - S140
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 9473 - 13
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 01/2017, Volume 120, Issue 1-2, pp. S131 - S132
Journal Article