X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (6) 6
female (5) 5
index medicus (5) 5
male (5) 5
child (4) 4
genetics & heredity (3) 3
pediatrics (3) 3
adolescent (2) 2
adult (2) 2
cerebellar disorders (2) 2
clinical neurology (2) 2
dysmorphology (2) 2
infant (2) 2
mutations (2) 2
30-day readmissions (1) 1
90-d (1) 1
abnormalities, multiple - diagnosis (1) 1
acidemia (1) 1
age (1) 1
aged (1) 1
aged, 80 and over (1) 1
amino acid metabolism, inborn errors - metabolism (1) 1
amino acid metabolism, inborn errors - pathology (1) 1
array-based comparative genomic hybridization (1) 1
ataxia (1) 1
automated facial analysis software (1) 1
automation (1) 1
batten-disease (1) 1
biochemistry, general (1) 1
cerebellar diseases - metabolism (1) 1
cerebellar diseases - pathology (1) 1
cerebral and cerebella dysmyelination (1) 1
cerebrofaciothoracic dysplasia (1) 1
child, preschool (1) 1
children (1) 1
cholecystectomy (1) 1
cholecystectomy - adverse effects (1) 1
cholecystectomy, laparoscopic - adverse effects (1) 1
cholelithiasis (1) 1
chromosome aberrations (1) 1
chromosomes, human, pair 19 (1) 1
cln3 (1) 1
cognition - physiology (1) 1
cognitive deficit (1) 1
cognitive profile (1) 1
congenital diseases (1) 1
congenital disorder (1) 1
congenital disorders of glycosylation (1) 1
corpus callosum hypogenesis (1) 1
d-2-hydroxyglutaric aciduria (1) 1
de-novo duplication (1) 1
deficiency (1) 1
deficit-hyperactivity disorder (1) 1
deletion (1) 1
direct duplication (1) 1
disabilities (1) 1
disease (1) 1
disease progression (1) 1
dna mutational analysis (1) 1
elective laparoscopic cholecystectomy (1) 1
emergency (1) 1
encephalopathy (1) 1
endocrinology & metabolism (1) 1
epidemiology (1) 1
face - abnormalities (1) 1
facial dysmorphia (1) 1
facio-thoracic dysplasia (1) 1
gastroenterology & hepatology (1) 1
general-surgery (1) 1
genetic research (1) 1
genetics, population (1) 1
genotype (1) 1
genotype & phenotype (1) 1
genotypes (1) 1
glutarates - chemistry (1) 1
glutarates - metabolism (1) 1
glycosylation (1) 1
hemangiomas (1) 1
hospital readmission (1) 1
hospitals, university (1) 1
human genetics (1) 1
ia cdg-ia (1) 1
image processing (1) 1
inclusions (1) 1
inpatients (1) 1
intellectual disability - diagnosis (1) 1
intelligence quotient (1) 1
internal medicine (1) 1
klinefelter syndrome (1) 1
l-2-hydroxiglutaric aciduria (1) 1
l-2-hydroxyglutaric aciduria (1) 1
learning difficulties (1) 1
lipodystrophy (1) 1
lysine - metabolism (1) 1
magnetic resonance (1) 1
magnetic resonance imaging (1) 1
malformations (1) 1
medical education (1) 1
medical research (1) 1
medicine & public health (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


ANALES DE PEDIATRIA, ISSN 1695-4033, 08/2017, Volume 87, Issue 2, pp. 73 - 77
Introduction: Neurofibromatosis type 1 (NF1) is a genetic disorder with various clinical manifestations that affect the peripheral and central nervous system,... 
Learning difficulties | COGNITIVE PROFILE | Neuropsychological performance | SKILLS | WISC-IV | PEDIATRICS | Neurofibromatosis type 1 | DEFICIT-HYPERACTIVITY DISORDER | Cognitive deficit | DISABILITIES | Intelligence quotient | CHILDREN | Neuropsychological Tests | Humans | Female | Male | Neurofibromatosis 1 - diagnosis | Neurofibromatosis 1 - physiopathology | Child
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 10/2011, Volume 34, Issue 5, pp. 1083 - 1093
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.