X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (249) 249
Patent (97) 97
Publication (48) 48
Book Chapter (10) 10
Book Review (2) 2
Conference Proceeding (2) 2
Book / eBook (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (154) 154
performing operations (86) 86
transporting (86) 86
lining machines (85) 85
printing (85) 85
stamps (85) 85
typewriters (85) 85
correction of typographical errors (84) 84
i.e. mechanisms printing otherwise than from a forme (84) 84
selective printing mechanisms (84) 84
male (74) 74
animals (68) 68
neurosciences (68) 68
index medicus (62) 62
clinical neurology (55) 55
female (51) 51
genetics & heredity (51) 51
mutation (45) 45
physics (42) 42
mice (41) 41
adult (39) 39
article (37) 37
electricity (34) 34
arrangements for measuring two or more variables not coveredin a single other subclass (33) 33
measuring (33) 33
measuring not specially adapted for a specific variable (33) 33
measuring or testing not otherwise provided for (33) 33
tariff metering apparatus (33) 33
testing (33) 33
middle aged (31) 31
biochemistry & molecular biology (29) 29
receptors, androgen - genetics (28) 28
gene (25) 25
nervous system diseases (25) 25
disease (24) 24
muscular atrophy, spinal - genetics (24) 24
adolescent (23) 23
genetics (22) 22
neurology (22) 22
androgen receptor (21) 21
electric communication technique (21) 21
expression (21) 21
pictorial communication, e.g. television (21) 21
aged (20) 20
pedigree (20) 20
charcot-marie-tooth disease - genetics (19) 19
child (19) 19
research (18) 18
x chromosome (18) 18
analysis (17) 17
genetic aspects (17) 17
genetic linkage (17) 17
huntingtons-disease (17) 17
protein (17) 17
disease models, animal (16) 16
mice, transgenic (16) 16
bulbar muscular-atrophy (15) 15
molecular sequence data (15) 15
mutations (15) 15
nervous system (15) 15
phenotype (15) 15
receptors, androgen - metabolism (15) 15
transgenic mouse model (15) 15
cells, cultured (14) 14
genes (14) 14
proteins (14) 14
spinal and bulbar muscular atrophy (14) 14
basic electric elements (13) 13
cell line (13) 13
electric solid state devices not otherwise provided for (13) 13
neurons (13) 13
peptides - metabolism (13) 13
semiconductor devices (13) 13
base sequence (12) 12
magnetic resonance imaging (12) 12
mouse model (12) 12
neurodegeneration (12) 12
peptides - genetics (12) 12
rats (12) 12
repetitive sequences, nucleic acid (12) 12
spinal muscular atrophy (12) 12
spinal muscular-atrophy (12) 12
amino acid sequence (11) 11
articles (11) 11
atrophy (11) 11
charcot-marie-tooth disease (11) 11
hereditary motor (11) 11
marie-tooth-disease (11) 11
motor neuron disease (11) 11
muscles (11) 11
muscular atrophy, spinal - metabolism (11) 11
neurodegenerative diseases (11) 11
cell biology (10) 10
child, preschool (10) 10
expanded polyglutamine (10) 10
research article (10) 10
sensory neuropathy (10) 10
survival (10) 10
transcription (10) 10
ataxia (9) 9
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The New England Journal of Medicine, ISSN 0028-4793, 06/2019, Volume 380, Issue 24, pp. 2373 - 2374
Huntington’s disease is a severe autosomal-dominant neurodegenerative disorder that involves chorea, cognitive decline, and psychological problems such as... 
Proteins | Huntingtons disease | Disease | Neurodegenerative diseases | Chorea | S gene | Cognitive ability | Population studies | Impulsive behavior | Chromosome 4 | Hereditary diseases
Journal Article
The New England journal of medicine, ISSN 0028-4793, 06/2019, Volume 380, Issue 24, pp. 2373 - 2374
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 07/2019, Volume 179, Issue 7, pp. 1122 - 1125
Journal Article
The Lancet Neurology, ISSN 1474-4422, 12/2018, Volume 17, Issue 12, pp. 1043 - 1052
Journal Article
Journal Article
Muscle & Nerve, ISSN 0148-639X, 01/2018, Volume 57, Issue 1, pp. 40 - 44
Journal Article
Scientific Reports, ISSN 2045-2322, 06/2016, Volume 6, Issue 1, p. 27703
  Polyglutamine expansion in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA), an X-linked neuromuscular disease that is fully... 
Journal Article
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 08/2017, Volume 27, Issue 8, p. 705
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1016/j.nmd.2017.04.008 
Care and treatment | Duchenne muscular dystrophy | Muscles | Diagnostic imaging
Journal Article
Science, ISSN 0036-8075, 6/2002, Volume 296, Issue 5575, pp. 1991 - 1995
A broad range of neurodegenerative disorders is characterized by neuronal damage that may be caused by toxic, aggregation-prone proteins. As genes are... 
Nervous system diseases | Reviews | Neurodegenerative diseases | Disease models | Huntington disease | Parkinson disease | Prion diseases | Amyotrophic lateral sclerosis | Nervous system heredodegenerative disorders | Alzheimers disease | Genetic mutation | Parkinson Disease - therapy | Neurons - pathology | Prion Diseases - genetics | Humans | Peptides - genetics | Tauopathies - pathology | Alzheimer Disease - pathology | Peptides - metabolism | Tauopathies - therapy | Neurons - metabolism | Parkinson Disease - metabolism | Inclusion Bodies - metabolism | Prion Diseases - therapy | Parkinson Disease - pathology | Neurodegenerative Diseases - pathology | Amyotrophic Lateral Sclerosis - therapy | Amyotrophic Lateral Sclerosis - genetics | Alzheimer Disease - therapy | Neurodegenerative Diseases - genetics | Neurodegenerative Diseases - therapy | Prion Diseases - pathology | Neurodegenerative Diseases - metabolism | Parkinson Disease - genetics | Protein Folding | Trinucleotide Repeat Expansion | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Tauopathies - metabolism | Animals | Proteins - metabolism | Alzheimer Disease - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Mutation | Proteins - chemistry | Alzheimer Disease - genetics | Prion Diseases - metabolism | Parkinson's disease | Nervous system | Degeneration | Research | Alzheimer's disease | Proteins | Neurological disorders
Journal Article
JAMA Neurology, ISSN 2168-6149, 05/2015, Volume 72, Issue 5, pp. 561 - 561
The family of genes implicated in hereditary spastic paraplegias (HSPs) is quickly expanding, mostly owing to the widespread availability of next-generation... 
Journal Article
Progress in Neurobiology, ISSN 0301-0082, 12/2012, Volume 99, Issue 3, pp. 257 - 261
Journal Article
Scientific reports, ISSN 2045-2322, 06/2016, Volume 6, p. 27703
Polyglutamine expansion in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA), an X-linked neuromuscular disease that is fully... 
Journal Article
Journal of Visualized Experiments, ISSN 1940-087X, 08/2018, Volume 2018, Issue 138
RNA interference via the endogenous miRNA pathway regulates gene expression by controlling protein synthesis through post-transcriptional gene silencing. In... 
rAAV | Gene silencing | Issue 138 | Neuromuscular disease | Genetics | miRNA | RNA therapeutics | Gene therapy | MULTIDISCIPLINARY SCIENCES | Neuromuscular Disease
Journal Article
Trends in Pharmacological Sciences, ISSN 0165-6147, 2010, Volume Okt, p. 523
Spinal and bulbar muscular atrophy is a hereditary motor neuron disease caused by trinucleotide repeat expansion in the androgen receptor gene. The disease... 
Basic Medicine | Neurosciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Neurovetenskaper
Journal Article
Lancet, ISSN 0140-6736, 8/2014, Volume 384, Issue 9942, pp. 474 - 475
Journal Article
No results were found for your search.

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