X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (73) 73
humans (54) 54
male (44) 44
middle aged (37) 37
female (35) 35
adult (28) 28
aged (28) 28
neurosciences (22) 22
mutation (20) 20
clinical neurology (19) 19
animals (17) 17
genetics & heredity (13) 13
genotype (13) 13
parkinson disease - genetics (13) 13
magnetic resonance imaging (12) 12
aged, 80 and over (11) 11
parkinson's disease (11) 11
biochemistry & molecular biology (10) 10
case-control studies (10) 10
genetics (10) 10
young adult (10) 10
association (9) 9
brain (9) 9
drosophila (9) 9
human necessities (9) 9
hygiene (9) 9
japan (9) 9
medical or veterinary science (9) 9
mice (9) 9
mutations (9) 9
preparations for medical, dental, or toilet purposes (9) 9
specific therapeutic activity of chemical compounds ormedicinal preparations (9) 9
adolescent (8) 8
gene (7) 7
genetic aspects (7) 7
medicine, general & internal (7) 7
oncology (7) 7
polymorphism (7) 7
risk factors (7) 7
age of onset (6) 6
alexander disease (6) 6
analysis (6) 6
astrocytes (6) 6
astrocytes - metabolism (6) 6
atrophy (6) 6
brain - pathology (6) 6
cadasil (6) 6
cadasil - diagnosis (6) 6
cadasil - genetics (6) 6
case report (6) 6
cells, cultured (6) 6
disease (6) 6
expression (6) 6
gastroenterology & hepatology (6) 6
genes (6) 6
nerve tissue proteins - genetics (6) 6
pedigree (6) 6
polymorphism, single nucleotide (6) 6
research (6) 6
alpha-synuclein (5) 5
amyotrophic lateral sclerosis (5) 5
astrocytes - drug effects (5) 5
base sequence (5) 5
child (5) 5
dementia (5) 5
diagnosis, differential (5) 5
gene frequency (5) 5
genetic predisposition to disease (5) 5
glial cell line-derived neurotrophic factor (5) 5
immunology (5) 5
japan - epidemiology (5) 5
molecular sequence data (5) 5
neurons (5) 5
notch3 (5) 5
receptor, notch3 - genetics (5) 5
rna (5) 5
time factors (5) 5
abridged index medicus (4) 4
alexander disease - genetics (4) 4
alpha-synuclein - genetics (4) 4
amyotrophic-lateral-sclerosis (4) 4
article (4) 4
astrocyte (4) 4
bdnf (4) 4
cell biology (4) 4
child, preschool (4) 4
diagnosis (4) 4
dna mutational analysis (4) 4
drosophila proteins - genetics (4) 4
exons (4) 4
family (4) 4
genetic screening (4) 4
gfap (4) 4
heterozygote (4) 4
homeostasis (4) 4
inflammation (4) 4
lewy bodies (4) 4
medical colleges (4) 4
medicine & public health (4) 4
mice, inbred icr (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 12/2009, Volume 41, Issue 12, pp. 1303 - 1307
Journal Article
Internal Medicine, ISSN 0918-2918, 2018, Volume 57, Issue 10, pp. 1463 - 1468
Journal Article
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, ISSN 1590-1874, 08/2019, pp. 1 - 3
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 05/2018, Volume 63, Issue 5, pp. 687 - 690
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), caused by NOTCH3, primarily affects small cerebral... 
MOYAMOYA-DISEASE | RNF213 | GENE | DIAGNOSTIC-CRITERIA | GENETICS & HEREDITY
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 11291 - 14
Fused in sarcoma (FUS) was identified as a component of typical inclusions in frontotemporal lobar degeneration (FTLD) and amyotrophic lateral sclerosis (ALS).... 
Motor neurons | Phenotypes | Sarcoma | Myeloid leukemia | FUS gene | Amyotrophic lateral sclerosis | Sclerosis | Genotype & phenotype | FUS protein | Insects | Inclusion bodies | Morphology | Degeneration | Imaginal discs | Fusion protein | Frontotemporal dementia
Journal Article
Experimental Neurology, ISSN 0014-4886, 03/2016, Volume 277, pp. 86 - 95
Journal Article
Internal Medicine, ISSN 0918-2918, 2018
A 65-year-old woman with rheumatoid arthritis (RA) visited our hospital because of right facial sensory hypoesthesia. Cerebral toxoplasmosis was suspected on... 
nested-PCR | methotrexate | rheumatoid arthritis | cerebral toxoplasmosis
Journal Article
NeuroReport, ISSN 0959-4965, 09/2019
AlkB family proteins are enzymes that repair alkylated DNA and RNA by oxidative demethylation. Nine homologs have been identified and characterized in mammals.... 
Index Medicus
Journal Article
JOURNAL OF NEUROINFLAMMATION, ISSN 1742-2094, 04/2019, Volume 16, Issue 1, pp. 79 - 79
Background: Microglia play crucial roles in the maintenance of brain homeostasis. Activated microglia show a biphasic influence, promoting beneficial repair... 
MACROPHAGES | Neuroinflammation | ISCHEMIA | ANGIOTENSIN-II | Proliferation | IMMUNOLOGY | BLOOD-BRAIN-BARRIER | NEUROSCIENCES | Cerebral small vessel disease | INFLAMMATION | Perivascular microglia | ACTIVATED MICROGLIA | Chronic hypertension | EXPRESSION | Mineralocorticoids - toxicity | Rats, Wistar | Ki-67 Antigen - metabolism | Male | Antigens, CD - metabolism | Hypertension - etiology | Time Factors | Carboxymethylcellulose Sodium - pharmacology | Microglia - pathology | Blood Pressure - drug effects | Microfilament Proteins - metabolism | Disease Models, Animal | Calcium-Binding Proteins - metabolism | Microglia - drug effects | Cell Proliferation - physiology | Rats | Functional Laterality | Sodium Chloride - toxicity | Hypertension - pathology | Brain - drug effects | Magnetic Resonance Imaging | Animals | Microglia - classification | Nephrectomy - adverse effects | Desoxycorticosterone Acetate - toxicity | Brain - pathology | Hypertension - complications | Cell Proliferation - drug effects | Hypertension - diagnostic imaging | Hypertension | Cell proliferation | Brain | Drinking water | Nuclear magnetic resonance--NMR | Laboratories | Homeostasis | Parenchyma | Inflammation | Injection | Sodium chloride | Microglia | Class switching | Blood-brain barrier | Ischemia | Nephrectomy | Rodents | Blood pressure | Acetic acid
Journal Article
Neuropathology, ISSN 0919-6544, 06/2014, Volume 34, Issue 3, pp. 309 - 313
Journal Article
Journal of Neurology, ISSN 0340-5354, 11/2011, Volume 258, Issue 11, pp. 1998 - 2008
Journal Article
Human genome variation, ISSN 2054-345X, 2017, Volume 4, Issue 1, pp. 17028 - 17028
Alexander disease (AxD) is a rare hereditary neurodegenerative disorder caused by glial fibrillary acidic protein ( ) gene mutations, most of which are... 
Mutation
Journal Article
Dementia and Geriatric Cognitive Disorders Extra, ISSN 1664-5464, 05/2016, Volume 6, Issue 2, pp. 183 - 184
Journal Article
Auris Nasus Larynx, ISSN 0385-8146, 08/2018, Volume 45, Issue 4, pp. 866 - 870
Cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome (CANVAS) is a novel ataxic disorder consisting of the triad of cerebellar... 
CANVAS | vHIT | VVOR | OTORHINOLARYNGOLOGY | Medical colleges | Ataxia | Index Medicus
Journal Article