Medicine and Dentistry
Mucopolysaccharidosis
100%
Mucolipidosis
75%
I-Cell Disease
64%
Hunter Syndrome
51%
Systematic Review
47%
Gene Therapy
47%
Hematopoietic Cell
47%
Cartilage Pathology
25%
Hip Disease
23%
Pseudo-Hurler Polydystrophy
23%
Engraftment
23%
Neonates
23%
Long Chain Acyl Coenzyme A Dehydrogenase
23%
Glutaric Acidemia Type 2
23%
Gene Expression
23%
Mevalonate Kinase Deficiency
23%
Newborn Screening
23%
Multiple Sulfatase Deficiency
23%
Dipeptidyl Peptidase I
23%
Lysosome Enzyme
23%
Riboflavin
23%
Cathepsin K
23%
Diseases
22%
Lysosomal Storage Disease
21%
Storage Disease
18%
Autosomal Recessive Inheritance
17%
Clinical Feature
17%
Glycosaminoglycan
15%
False Positive Result
15%
Neurologic Disease
15%
Quality of Life
14%
N Acetylgalactosamine 4 Sulfatase
13%
Riboflavin Deficiency
11%
Sulfatase
11%
Mucolipidosis Type IV
11%
Disease
11%
Skeleton Malformation
9%
Hip Joint
7%
Counseling
7%
Therapy Development
7%
Neonatal Infant
7%
Blood Brain Barrier
7%
Acylcarnitine
7%
Ataxia
7%
Water-Electrolyte Imbalance
7%
Transient Receptor Potential Channel
5%
Cation Channel
5%
Pycnodysostosis
5%
Mannose 6 Phosphate
5%
Mammalian Target of Rapamycin
5%
Biochemistry, Genetics and Molecular Biology
Mucopolysaccharidosis
94%
Iduronate-2-Sulfatase
70%
Gene Therapy
47%
Hematopoietic Cell
47%
Enzyme
30%
Mass Spectrometry
25%
Maroteaux-Lamy Syndrome
23%
Oligosaccharide
23%
Gene Expression
23%
High-Performance Liquid Chromatography
23%
Riboflavin
23%
Glycosaminoglycan
19%
Titer
16%
Arylsulfatase B
13%
GM2 Gangliosidoses
11%
Mannosidosis
11%
Mucolipidosis
11%
Blood Brain Barrier
7%
Aspartylglucosaminuria
5%
GM1 Gangliosidosis
5%
Fucosidosis
5%
Deglycosylation
5%
Lysosome
5%
Sphingolipidoses
5%
Galactosialidosis
5%
Sialidosis
5%
Thin-Layer Chromatography
5%
Quality Control
5%
Glycolipid
5%
Polysaccharides
5%
Sialic Acid
5%
Bioinformatics
5%
Tetrasaccharide
5%
Pharmacology, Toxicology and Pharmaceutical Science
Mucopolysaccharidosis
47%
Hunter Syndrome
29%
Mucolipidosis Type 2
23%
Mucopolysaccharidosis Type 7
23%
Vestronidase Alfa
23%
Inborn Error of Metabolism
23%
Mucolipidosis Type 3
23%
Iduronate 2 Sulfatase
23%
Cathepsin K
23%
Diseases
23%
Glycosaminoglycan
14%
Dermatan Sulfate
8%
Chondroitin Sulfate
8%
Biological Marker
7%
Stable Isotope
7%
Heparan Sulfate
5%
Beta Glucuronidase
5%
Lysosome Storage Disease
5%
