X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (6974) 6974
Newsletter (1319) 1319
Book Review (588) 588
Publication (363) 363
Newspaper Article (157) 157
Conference Proceeding (50) 50
Magazine Article (42) 42
Dissertation (33) 33
Book Chapter (29) 29
Book / eBook (3) 3
Government Document (3) 3
Trade Publication Article (3) 3
Transcript (3) 3
Streaming Video (2) 2
Web Resource (2) 2
Journal / eJournal (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (4904) 4904
humans (4827) 4827
mucopolysaccharidosis (3690) 3690
male (2368) 2368
female (2071) 2071
child (1614) 1614
genetics & heredity (1296) 1296
animals (1278) 1278
child, preschool (1246) 1246
enzymes (1180) 1180
adolescent (992) 992
research (976) 976
adult (939) 939
enzyme replacement therapy (875) 875
infant (795) 795
glycosaminoglycans (787) 787
medicine, research & experimental (754) 754
pediatrics (748) 748
care and treatment (709) 709
mice (674) 674
disease (653) 653
medical research (624) 624
medicine, experimental (592) 592
analysis (556) 556
mutation (539) 539
biochemistry & molecular biology (536) 536
diagnosis (511) 511
health aspects (502) 502
old medline (481) 481
reports (478) 478
mucopolysaccharidosis i (470) 470
children (456) 456
glycosaminoglycans - metabolism (448) 448
gene therapy (438) 438
radiography (435) 435
abridged index medicus (434) 434
transplantation (428) 428
disease models, animal (422) 422
phenotype (414) 414
glycosaminoglycans - urine (396) 396
bone-marrow-transplantation (376) 376
endocrinology & metabolism (366) 366
lysosomal storage diseases (358) 358
mucopolysaccharidosis i - genetics (358) 358
mucopolysaccharidosis ii - genetics (348) 348
mucopolysaccharidoses (334) 334
lysosomal storage disease (330) 330
genetic aspects (313) 313
mucopolysaccharidosis i - diagnosis (309) 309
cells, cultured (302) 302
enzyme-replacement therapy (301) 301
diagnosis, differential (295) 295
mucopolysaccharidosis i - pathology (293) 293
infant, newborn (292) 292
mucopolysaccharidosis iv - genetics (291) 291
sulfates (288) 288
mucopolysaccharidosis i - therapy (282) 282
treatment outcome (279) 279
hunter syndrome (278) 278
hematopoietic stem cells (276) 276
mucopolysaccharidosis type-vii (273) 273
expression (270) 270
biotechnology & applied microbiology (264) 264
genetics (264) 264
mouse model (246) 246
brain (245) 245
young adult (245) 245
article (243) 243
mucopolysaccharidosis iv - diagnosis (243) 243
mucopolysaccharidosis i - complications (237) 237
hurler-syndrome (236) 236
mucopolysaccharidosis iii - genetics (234) 234
identification (233) 233
medicine (232) 232
mucopolysaccharidosis ii - diagnosis (232) 232
medicine & public health (230) 230
molecular sequence data (229) 229
neurosciences (225) 225
biopharmaceutics (224) 224
middle aged (222) 222
mucopolysaccharidosis iv (222) 222
base sequence (221) 221
pedigree (221) 221
genes (220) 220
alpha-l-iduronidase (218) 218
fibroblasts (217) 217
mucopolysaccharidoses - diagnosis (217) 217
pathology (217) 217
clinical neurology (212) 212
pregnancy (212) 212
central-nervous-system (211) 211
lysosomal storage disorders (208) 208
mutations (208) 208
genetic therapy (207) 207
gene (205) 205
fibroblasts - enzymology (204) 204
stem cells (202) 202
brain - pathology (199) 199
metabolic diseases (197) 197
genetic research (192) 192
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (7429) 7429
French (325) 325
German (172) 172
Spanish (144) 144
Italian (133) 133
Japanese (84) 84
Portuguese (55) 55
Polish (51) 51
Russian (51) 51
Chinese (36) 36
Czech (21) 21
Hungarian (12) 12
Turkish (10) 10
Dutch (9) 9
Danish (6) 6
Korean (5) 5
Romanian (4) 4
Croatian (3) 3
Serbian (3) 3
Slovak (3) 3
Bulgarian (2) 2
Finnish (2) 2
Indonesian (2) 2
Norwegian (2) 2
Swedish (2) 2
Hebrew (1) 1
Persian (1) 1
Ukrainian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Pediatric Pulmonology, ISSN 8755-6863, 03/2014, Volume 49, Issue 3, pp. 277 - 284
BackgroundThe 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 | TAIWAN | 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 | Index Medicus
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 | Index Medicus | 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
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, pp. e0156452 - 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 | Index Medicus
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
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2014, Volume 111, Issue 2, pp. 128 - 132
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 06/2017, Volume 121, Issue 2, pp. 70 - 79
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 05/2013, Volume 109, Issue 1, pp. 54 - 61
Journal Article