X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (64) 64
index medicus (48) 48
mucopolysaccharidosis (48) 48
male (37) 37
child (35) 35
female (35) 35
adolescent (29) 29
child, preschool (27) 27
genetics & heredity (27) 27
enzymes (25) 25
pediatrics (19) 19
adult (18) 18
research (18) 18
children (17) 17
disease (17) 17
infant (17) 17
lysosomal storage diseases (16) 16
medicine, research & experimental (15) 15
mucopolysaccharidosis iii - epidemiology (15) 15
enzyme replacement therapy (14) 14
care and treatment (13) 13
incidence (13) 13
medicine (13) 13
mucopolysaccharidosis iii - genetics (13) 13
mutation (13) 13
diagnosis (12) 12
young adult (12) 12
health aspects (11) 11
mucopolysaccharidoses (11) 11
age (10) 10
patients (10) 10
genetics (9) 9
lysosomal storage disorders (9) 9
mucopolysaccharidoses - epidemiology (9) 9
mucopolysaccharidosis iii - diagnosis (9) 9
phenotype (9) 9
prevalence (9) 9
retrospective studies (9) 9
review (9) 9
analysis (8) 8
development and progression (8) 8
epidemiology (8) 8
glycosaminoglycans (8) 8
metabolism (8) 8
pharmacology (8) 8
animals (7) 7
disorders (7) 7
enzyme-replacement therapy (7) 7
lysosomal storage disease (7) 7
metabolic disorders (7) 7
middle aged (7) 7
sanfilippo syndrome (7) 7
bone-marrow-transplantation (6) 6
frequency (6) 6
genetic disorders (6) 6
medical research (6) 6
mucopolysaccharidosis iii - complications (6) 6
reports (6) 6
treatment outcome (6) 6
age of onset (5) 5
comorbidity (5) 5
cross-sectional studies (5) 5
disease progression (5) 5
diseases (5) 5
dna mutational analysis (5) 5
drugs (5) 5
endocrinology & metabolism (5) 5
follow-up studies (5) 5
genetic aspects (5) 5
heterogeneity (5) 5
identification (5) 5
internal medicine (5) 5
life sciences (5) 5
medical screening (5) 5
medicine, experimental (5) 5
mucopolysaccharidosis ii - epidemiology (5) 5
natural-history (5) 5
neurosciences (5) 5
patient outcomes (5) 5
prevalence studies (5) 5
risk factors (5) 5
studies (5) 5
therapy (5) 5
age factors (4) 4
allelic heterogeneity (4) 4
behavior (4) 4
biochemistry, general (4) 4
hematopoietic stem cells (4) 4
hunter syndrome (4) 4
hunter-syndrome (4) 4
infant, newborn (4) 4
infants (4) 4
lysergide (4) 4
magnetic resonance imaging (4) 4
management (4) 4
medicine & public health (4) 4
metabolic diseases (4) 4
molecular analysis (4) 4
mucopolysaccharidoses - diagnosis (4) 4
mucopolysaccharidosis i - epidemiology (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


American Journal of Medical Genetics, Part A, ISSN 1552-4825, 01/2011, Volume 155, Issue 1, pp. 58 - 68
Journal Article
Journal of Autism and Developmental Disorders, ISSN 0162-3257, 11/2017, Volume 47, Issue 11, pp. 3620 - 3633
The prevalence of autism spectrum disorder (ASD) in many genetic disorders is well documented but not as yet in Mucopolysaccharidosis type III (MPS III). MPS... 
Pediatrics | Child and School Psychology | Neurosciences | Public Health | ASD | Psychology | Lysosomal storage disorder | Behavioural difficulties | Speech/language delay | Developmental disorder | Mucopolysacchardosis | DIAGNOSIS | RARE | PSYCHOLOGY, DEVELOPMENTAL | CHILDREN | Diagnostic Tests | Comorbidity | Behavior Disorders | Infants | Personality Measures | Genetic Disorders | Speech Impairments | Interests | Intelligence Tests | Autism | Communication Problems | Pervasive Developmental Disorders | Literature Reviews | Language Impairments | Observation | Cognitive Ability | Child Development | Interpersonal Competence | Clinical Diagnosis | Symptoms (Individual Disorders) | Mucopolysaccharidosis III - diagnosis | Autism Spectrum Disorder - epidemiology | Diagnostic Errors | Humans | Middle Aged | Adolescent | Adult | Female | Male | Mucopolysaccharidosis III - epidemiology | Child | Autism Spectrum Disorder - diagnosis | Psychological aspects | Care and treatment | Pervasive developmental disorders | Mucopolysaccharidosis | Research | Diagnosis | Prevalence studies (Epidemiology) | Genetic disorders | Misdiagnosis | Medical diagnosis | Counselling | Literature reviews | Repetitive behaviour | Systematic reviews | Speech | Genetic counselling | Symptoms | Metabolic disorders | language delay | Original Paper
Journal Article
Vestnik Rossiiskoi akademii meditsinskikh nauk, ISSN 0869-6047, 2015, Issue 4, p. 419
Sanfilippo syndrome (mucopolysaccharidosis type III) is a lysosomal disorder caused by a defect in the catabolism of heparan sulfate. Mucopolysaccharidosis... 
Morbidity - trends | Mucopolysaccharidosis III - diagnosis | Genetic Predisposition to Disease | Global Health | Mucopolysaccharidosis III - genetics | Humans | Fibroblasts - pathology | Mucopolysaccharidosis III - epidemiology
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 1997, Volume 6, Issue 5, pp. 787 - 791
Journal Article
Clinical Genetics, ISSN 0009-9163, 1986, Volume 29, Issue 2, pp. 129 - 132
Journal Article