X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (141) 141
thin corpus-callosum (114) 114
index medicus (112) 112
clinical neurology (93) 93
female (87) 87
male (87) 87
spastic paraplegia, hereditary - genetics (84) 84
adult (76) 76
hereditary spastic paraplegia (76) 76
neurosciences (72) 72
mutation (57) 57
spg11 (56) 56
magnetic resonance imaging (51) 51
proteins - genetics (51) 51
spastic paraplegia, hereditary - pathology (47) 47
mutations (43) 43
phenotype (42) 42
spatacsin (42) 42
thin corpus callosum (42) 42
pedigree (38) 38
adolescent (37) 37
paralysis, spastic (37) 37
middle aged (36) 36
neurology (36) 36
young adult (35) 35
paraparesis (32) 32
corpus callosum - pathology (31) 31
brain - pathology (30) 30
genetic aspects (30) 30
spastic paraplegia, hereditary - diagnosis (30) 30
genetics & heredity (29) 29
animals (27) 27
spastic paraplegia (27) 27
child (25) 25
gene (24) 24
paraplegia (23) 23
corpus callosum (21) 21
diagnosis (20) 20
locus (20) 20
spastic paraplegia, hereditary - physiopathology (20) 20
dna mutational analysis (19) 19
neuroimaging (19) 19
research (19) 19
spectrum (19) 19
brain (18) 18
genetics (18) 18
heat shock proteins (18) 18
child, preschool (17) 17
genetic-heterogeneity (17) 17
frequent (16) 16
mutation - genetics (16) 16
nervous system diseases (16) 16
genotype (15) 15
linkage (15) 15
paralysis (15) 15
article (14) 14
genes (14) 14
life sciences (14) 14
aged (13) 13
disease (13) 13
genes, recessive (13) 13
heterogeneity (13) 13
magnetic resonance imaging - methods (13) 13
amyotrophic-lateral-sclerosis (12) 12
base sequence (12) 12
degeneration (12) 12
diffusion tensor imaging (12) 12
genetic research (12) 12
medicine & public health (12) 12
proteins (12) 12
radiology, nuclear medicine & medical imaging (12) 12
abridged index medicus (11) 11
ataxia (11) 11
family health (11) 11
mri (11) 11
brain - metabolism (10) 10
families (10) 10
gene mutations (10) 10
genetic disorders (10) 10
mental impairment (10) 10
neurons and cognition (10) 10
physiological aspects (10) 10
spastic paraplegia, hereditary - diagnostic imaging (10) 10
spasticity (10) 10
spg11 mutations (10) 10
[sdv.neu]life sciences [q-bio]/neurons and cognition [q-bio.nc] (9) 9
amyotrophic lateral sclerosis (9) 9
analysis (9) 9
atrophy (9) 9
autosomal-dominant (9) 9
neurodegeneration (9) 9
rats (9) 9
risk factors (9) 9
spastic paraplegia, hereditary (9) 9
spg15 (9) 9
agenesis of corpus callosum (8) 8
biochemistry & molecular biology (8) 8
care and treatment (8) 8
chromatography, thin layer (8) 8
consanguinity (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Neuroradiology, ISSN 0028-3940, 06/2017, Volume 59, Issue 6, pp. 563 - 570
Journal Article
Clinical Genetics, ISSN 0009-9163, 10/2015, Volume 88, Issue 4, pp. 327 - 335
Journal Article
Brain, ISSN 0006-8950, 3/2008, Volume 131, Issue 3, pp. 772 - 784
Journal Article
Psychiatry Research: Neuroimaging, ISSN 0925-4927, 2010, Volume 183, Issue 2, pp. 126 - 132
Journal Article
Journal of Pediatric Neurosciences, ISSN 1817-1745, 07/2015, Volume 10, Issue 3, pp. 273 - 275
Infantile tremor syndrome (ITS) is a clinical disorder characterized by coarse tremors, anemia and regression of motor and mental milestones, presenting in... 
Vitamin B12 | Infantile tremor syndrome | thin corpus callosum | Proteins | Hair | Medical imaging | Sleep | Anemia | Conflicts of interest | Malnutrition | Children & youth | Case Report
Journal Article