Medicine & Life Sciences
Mucopolysaccharidosis I
100%
Mutation
47%
Mucopolysaccharidoses
45%
Inborn Urea Cycle Disorder
44%
Phenotype
41%
Neonatal Screening
40%
Genes
38%
Mucopolysaccharidosis II
38%
Iduronidase
35%
Enzyme Replacement Therapy
32%
Mucopolysaccharidosis III
31%
Lissencephaly
29%
Child
27%
glycerol phenylbutyrate
26%
Mucopolysaccharidosis VI
25%
Glycosaminoglycans
21%
Brain
21%
Growth Hormone
20%
Papillorenal syndrome
17%
Classical Lissencephalies and Subcortical Band Heterotopias
17%
Liver
16%
Inborn Errors Metabolism
16%
Iduronate Sulfatase
15%
Enzymes
14%
Intellectual Disability
14%
Genetic Therapy
14%
Therapeutics
13%
Growth
13%
Noonan Syndrome
12%
Ammonia
12%
Periventricular Nodular Heterotopia
12%
Microcephaly
12%
Phenylketonurias
12%
Gangliosidoses
11%
Carnitine
11%
Serine Proteinase Inhibitors
10%
Genetic Testing
10%
Exons
10%
Inborn Genetic Diseases
10%
Growth Hormone-Releasing Hormone
10%
vestronidase alfa
10%
Newborn Infant
10%
Pediatrics
10%
Messenger RNA
10%
Siblings
9%
Malformations of Cortical Development
9%
Genetic Association Studies
9%
phenylacetic acid
9%
Proteins
9%
GM1 Gangliosidosis
9%
Genetic Counseling
9%
4-phenylbutyric acid
9%
Chromosomes
9%
Eye
9%
Cerebellar Hypoplasia
9%
Neurodevelopmental Disorders
8%
Zebrafish
8%
Cardiomyopathies
8%
Biomarkers
8%
Dystonia 12
8%
Population
8%
Safety
8%
Mucopolysaccharidosis VII
8%
Bone Marrow Transplantation
8%
Lysosomal acid lipase deficiency
8%
phenylacetylglutamine
8%
Genotype
8%
N-Acetylgalactosamine-4-Sulfatase
8%
Polymicrogyria
8%
Marfan Syndrome
8%
Cell Transplantation
7%
Rare Diseases
7%
Kidney
7%
Dilatation
7%
Agenesis of Cerebellar Vermis
7%
Lysosomal Storage Diseases
7%
Exome
7%
Heart Diseases
7%
Bioreactors
7%
Parents
6%
Neurofibromatosis 1
6%
Alleles
6%
Autism Spectrum Disorder
6%
Hearing
6%
Hematopoietic Stem Cell Transplantation
6%
Medical Genetics
6%
GM2 Gangliosidosis
6%
Natural History
6%
Gene Deletion
6%
Hexosaminidases
6%
Turkeys
6%
Information Systems
6%
Neuroimaging
6%
Glutamine
6%
Registries
6%
DNA
5%
Central Nervous System
5%
Ornithine Carbamoyltransferase Deficiency Disease
5%
Gene Editing
5%