X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (329) 329
Patent (96) 96
Publication (42) 42
Book Chapter (25) 25
Book Review (25) 25
Book / eBook (4) 4
Conference Proceeding (3) 3
Data Set (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (185) 185
humans (169) 169
male (91) 91
female (83) 83
clinical neurology (77) 77
physics (77) 77
adult (72) 72
middle aged (65) 65
neurosciences (64) 64
information storage (60) 60
static stores (50) 50
ataxia (48) 48
spinocerebellar ataxias - genetics (45) 45
mutation (42) 42
genetics & heredity (39) 39
neurology (39) 39
spinocerebellar ataxia (39) 39
abridged index medicus (34) 34
article (34) 34
electricity (34) 34
aged (33) 33
animals (31) 31
expansion (28) 28
genetics (28) 28
gene (27) 27
phenotype (27) 27
age of onset (26) 26
myotonic dystrophy - genetics (25) 25
alleles (24) 24
basic electric elements (22) 22
disease (22) 22
pedigree (22) 22
congenital, hereditary, and neonatal diseases and abnormalities (21) 21
electric solid state devices not otherwise provided for (21) 21
genes (21) 21
genetic aspects (21) 21
myotonic dystrophy (21) 21
semiconductor devices (21) 21
child (19) 19
molecular sequence data (19) 19
nerve tissue proteins - genetics (19) 19
trinucleotide repeat expansion - genetics (19) 19
trinucleotide repeats (19) 19
adolescent (18) 18
analysis (18) 18
research (18) 18
spinocerebellar ataxias (18) 18
biochemistry & molecular biology (17) 17
biomedicine (17) 17
mice (17) 17
spinocerebellar ataxias - pathology (17) 17
trinucleotide repeat (17) 17
cerebellar ataxia (16) 16
cerebellum (16) 16
genotype (16) 16
nervous system diseases (16) 16
polymerase chain reaction (16) 16
dna (15) 15
dna repeat expansion - genetics (15) 15
proteins (15) 15
epilepsy (14) 14
neurodegeneration (14) 14
rna (14) 14
sca10 (14) 14
testing (14) 14
age (13) 13
base sequence (13) 13
chemistry (13) 13
clinical-features (13) 13
ctg repeat (13) 13
myotonic-dystrophy (13) 13
aged, 80 and over (12) 12
brain (12) 12
cell biology (12) 12
families (12) 12
machado-joseph-disease (12) 12
measuring (12) 12
metallurgy (12) 12
repetitive sequences, nucleic acid (12) 12
severity of illness index (12) 12
young adult (12) 12
ataxin-10 (11) 11
huntington's disease (11) 11
medicine (11) 11
mutations (11) 11
neurobiology (11) 11
research article (11) 11
spinocerebellar ataxia type 10 (11) 11
cag repeat (10) 10
disease progression (10) 10
expression (10) 10
human necessities (10) 10
hygiene (10) 10
information storage based on relative movement between recordcarrier and transducer (10) 10
investigating or analysing materials by determining theirchemical or physical properties (10) 10
medical or veterinary science (10) 10
microsatellite repeats (10) 10
multidisciplinary sciences (10) 10
preparations for medical, dental, or toilet purposes (10) 10
psychiatry (10) 10
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (437) 437
Japanese (11) 11
Chinese (10) 10
Portuguese (10) 10
French (8) 8
Korean (3) 3
German (2) 2
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Lancet Neurology, ISSN 1474-4422, 04/2018, Volume 17, Issue 4, pp. 292 - 294
Spinocerebellar ataxias are a group of autosomal dominant neurodegenerative disorders, most of which show relentless progression, often resulting in total... 
CANCER | COHORT | CLINICAL NEUROLOGY | Longitudinal Studies | Humans | Spinocerebellar Ataxias | Cohort Studies | Nanoparticles | Disease | Medical prognosis | Spinocerebellar ataxia | Clinical trials | Ataxia | Patients | Natural history | Cancer | Index Medicus
Journal Article
Nature reviews. Neurology, ISSN 1759-4758, 12/2018, Volume 14, Issue 12, pp. 749 - 749
In Table 3 of this article as originally published, a sentence within the column "Comments" in the row "SCA6" contains an error. The text incorrectly reads... 
Journal Article
Neuron, ISSN 0896-6273, 08/2012, Volume 75, Issue 3, pp. 437 - 450
Journal Article
Journal Article
2006, 2nd ed., ISBN 9780123694621
This book describes everything about DNA repeat instability and neurological disorders, covering molecular mechanisms of repeat expansion, pathogenic... 
Trinucleotide Repeats | genetics | Neurogenetics | Chromosome Aberrations | Genetic Diseases, Inborn | Nervous system | Genetic aspects | Nervous System Diseases | Diseases
Web Resource
The Cerebellum, ISSN 1473-4222, 08/2019, pp. 1 - 6
Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant disorder in which patients have a slowly progressive cerebellar ataxia, with dysarthria,... 
Cerebellum | Phenotypes | Statistical analysis | Tremor | Cerebellar ataxia | Epilepsy | Phenotypic variations | Epidemiology | Hereditary diseases | Motivation | Ataxia | Dysphagia | Age | Genotypes | Index Medicus
Journal Article
Cell Reports, ISSN 2211-1247, 01/2012, Volume 1, Issue 1, pp. 2 - 12
Journal Article
Journal Article