X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (21) 21
index medicus (20) 20
enfant (18) 18
male (15) 15
clinical neurology (14) 14
female (14) 14
child (11) 11
neurology (9) 9
pediatrics (8) 8
child, preschool (7) 7
épilepsie (7) 7
dystonia (6) 6
magnetic resonance imaging (6) 6
adolescent (5) 5
childhood (5) 5
genetics & heredity (5) 5
infant (5) 5
mutation (5) 5
adult (4) 4
ataxia (4) 4
case report (4) 4
children (4) 4
diagnosis (4) 4
encephalitis (4) 4
genetic aspects (4) 4
medical imaging (4) 4
movement disorders (4) 4
nuclear magnetic resonance--nmr (4) 4
pedigree (4) 4
phenotype (4) 4
auto-immune (3) 3
brain (3) 3
consanguinity (3) 3
encéphalite (3) 3
epilepsy (3) 3
genetics (3) 3
joubert syndrome (3) 3
mouvements anormaux (3) 3
parkinsonism (3) 3
patients (3) 3
short communication (3) 3
siblings (3) 3
substantia nigra (3) 3
tunisia (3) 3
accident vasculaire cérébral (2) 2
age (2) 2
amino acid metabolism, inborn errors - complications (2) 2
amino acid metabolism, inborn errors - genetics (2) 2
antibodies (2) 2
biotechnology & applied microbiology (2) 2
calcification (2) 2
causes of (2) 2
cerebellar diseases - genetics (2) 2
cerebellum - abnormalities (2) 2
chorea (2) 2
clinical note (2) 2
creatine (2) 2
deletion (2) 2
diseases (2) 2
disorders (2) 2
encephalitis - complications (2) 2
encephalitis - pathology (2) 2
encephalocele - genetics (2) 2
encéphalopathie (2) 2
enzymes (2) 2
epidemiology (2) 2
eye abnormalities - genetics (2) 2
family medical history (2) 2
gaucher disease - genetics (2) 2
genotype (2) 2
glucosylceramidase - genetics (2) 2
génétique (2) 2
hyperglycemia - complications (2) 2
intellectual disability - genetics (2) 2
involvement (2) 2
kidney diseases, cystic - genetics (2) 2
leukodystrophy (2) 2
life sciences (2) 2
limbic encephalitis (2) 2
longitudinal studies (2) 2
medical laboratory technology (2) 2
medicine (2) 2
medicine, research & experimental (2) 2
mental retardation (2) 2
microcephaly (2) 2
middle aged (2) 2
mutation - genetics (2) 2
myoclonus (2) 2
myélite (2) 2
neuroimaging (2) 2
nmda (2) 2
parkinson's disease (2) 2
parkinsonian disorders - etiology (2) 2
parkinsonian disorders - pathology (2) 2
phenotypes (2) 2
proteins (2) 2
receptor (2) 2
research (2) 2
retina - abnormalities (2) 2
retrospective studies (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain & Development, ISSN 0387-7604, 2012, Volume 35, Issue 2, pp. 186 - 186
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 09/2016, Volume 53, Issue 9, pp. 608 - 615
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2018, Volume 174, pp. S134 - S134
Journal Article
Journal Article
Brain and Development, ISSN 0387-7604, 10/2017, Volume 39, Issue 9, pp. 751 - 755
Journal Article
BRAIN & DEVELOPMENT, ISSN 0387-7604, 10/2017, Volume 39, Issue 9, pp. 815 - 815
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 05/2014, Volume 9, Issue 1, pp. 72 - 72
Journal Article
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2018, Volume 174, pp. S126 - S126
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2018, Volume 174, pp. S30 - S30
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2018, Volume 174, pp. S63 - S64
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2018, Volume 174, pp. S156 - S157
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2019, Volume 175, pp. S51 - S52
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2019, Volume 175, pp. S59 - S59
Journal Article
Revue Neurologique, ISSN 0035-3787, 04/2019, Volume 175, pp. S17 - S17
Journal Article
Journal Article
No results were found for your search.

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