X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (12) 12
index medicus (12) 12
female (9) 9
adult (8) 8
male (8) 8
spastic paraplegia, hereditary - genetics (8) 8
clinical neurology (7) 7
kjellin-syndrome (7) 7
pedigree (7) 7
spatacsin (7) 7
hereditary spastic paraplegia (6) 6
mutation (6) 6
proteins - genetics (6) 6
spg11 (6) 6
genetics & heredity (5) 5
thin corpus-callosum (5) 5
adolescent (4) 4
degeneration (4) 4
family health (4) 4
genetic-heterogeneity (4) 4
neurosciences (4) 4
child (3) 3
corpus callosum - pathology (3) 3
dementia (3) 3
frequent (3) 3
hereditary spastic paraparesis (3) 3
identification (3) 3
kjellin's syndrome (3) 3
locus (3) 3
magnetic resonance imaging (3) 3
middle aged (3) 3
mutations (3) 3
paralysis (3) 3
paraparesis (3) 3
paraplegia (3) 3
phenotype (3) 3
spastic paraplegia (3) 3
spastic paraplegia, hereditary - pathology (3) 3
thin corpus callosum (3) 3
young adult (3) 3
aged (2) 2
autosomal recessive (2) 2
base sequence (2) 2
child, preschool (2) 2
chromosome mapping (2) 2
corpus callosum (2) 2
deletion (2) 2
dementia - complications (2) 2
dementia - genetics (2) 2
dna mutational analysis (2) 2
gene (2) 2
genes, recessive (2) 2
genetic disorders (2) 2
genetic linkage (2) 2
genomics (2) 2
genotype (2) 2
heat shock proteins (2) 2
heterogeneity (2) 2
kjellin syndrome (2) 2
linkage (2) 2
lod score (2) 2
medical and health sciences (2) 2
medicin och hälsovetenskap (2) 2
mental impairment (2) 2
neurology (2) 2
ophthalmology (2) 2
paralysis, spastic (2) 2
paraplegia - genetics (2) 2
psychiatry (2) 2
spastic paraplegia, hereditary - complications (2) 2
spectrum (2) 2
spg11 mutations (2) 2
spg15 (2) 2
tunisia (2) 2
14q22-q24 (1) 1
14q22–q24 (1) 1
abnormalities (1) 1
abnormalities, multiple - genetics (1) 1
adenosine triphosphatases - genetics (1) 1
adenosine triphosphatases - metabolism (1) 1
agenesis of corpus callosum (1) 1
alleles (1) 1
alu elements (1) 1
alu-mediated nonallelic homologous recombination (1) 1
amino acid metabolism, inborn errors - genetics (1) 1
amino acid metabolism, inborn errors - pathology (1) 1
amino acid metabolism, inborn errors - physiopathology (1) 1
amino acid sequence (1) 1
amino-acids (1) 1
amyotrophic-lateral-sclerosis (1) 1
analysis (1) 1
animals (1) 1
anopheles (1) 1
antibody (1) 1
article (1) 1
ataxia (1) 1
autosomal-dominant (1) 1
biomedicine (1) 1
brain - diagnostic imaging (1) 1
brain - metabolism (1) 1
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 B: Neuropsychiatric Genetics, ISSN 1552-4841, 10/2009, Volume 150, Issue 7, pp. 984 - 992
Journal Article
Acta Neurologica Scandinavica, ISSN 0001-6314, 09/2018, Volume 138, Issue 3, pp. 245 - 250
Journal Article
Journal Article
Journal Article
No results were found for your search.

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