X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
gba (5) 5
humans (5) 5
index medicus (5) 5
genetic aspects (4) 4
analysis (3) 3
female (3) 3
genetics & heredity (3) 3
glucocerebrosidase (3) 3
lrrk2 (3) 3
male (3) 3
middle aged (3) 3
parkinson disease - genetics (3) 3
parkinson's disease (3) 3
aged (2) 2
association study (2) 2
beta-glucosidase - genetics (2) 2
care and treatment (2) 2
cellular and molecular neuroscience (2) 2
clinical neurology (2) 2
dj-1 (2) 2
gaucher disease (2) 2
genome-wide association studies (2) 2
glucosylceramidase - genetics (2) 2
mapt (2) 2
medicine, research & experimental (2) 2
mice (2) 2
molecular biology (2) 2
mutation (2) 2
mutation - genetics (2) 2
neurosciences (2) 2
parkin (2) 2
pink1 (2) 2
protein (2) 2
research article (2) 2
snca (2) 2
usage (2) 2
activation (1) 1
adhd (1) 1
adult (1) 1
age of onset (1) 1
aged, 80 and over (1) 1
alpha-synuclein - genetics (1) 1
analysis of variance (1) 1
anatomy & morphology (1) 1
animals (1) 1
antigens, cd - genetics (1) 1
antigens, cd - metabolism (1) 1
antigens, cd19 - genetics (1) 1
antigens, cd19 - metabolism (1) 1
ashkenazi jewish (1) 1
ashkenazi jews (1) 1
attention-deficit hyperactivity disorder (1) 1
autism (1) 1
b cells (1) 1
bcr (1) 1
biochemistry & molecular biology (1) 1
biomedicine (1) 1
blood (1) 1
brain (1) 1
cadps2 (1) 1
cancer (1) 1
case-control studies (1) 1
cd79 antigens - genetics (1) 1
cd79 antigens - metabolism (1) 1
cell biology (1) 1
cells (1) 1
children (1) 1
cognition disorders - diagnostic imaging (1) 1
cognition disorders - etiology (1) 1
cognition disorders - genetics (1) 1
cognitive ability (1) 1
complications and side effects (1) 1
conditional knockout (1) 1
cre-iox (1) 1
cre-lox (1) 1
deg analysis (1) 1
diagnosis (1) 1
differentiation (1) 1
disease models, animal (1) 1
disorders (1) 1
dna mutational analysis (1) 1
dopamine neurons (1) 1
down-regulation (1) 1
dried blood spot (1) 1
endocrinology & metabolism (1) 1
expression (1) 1
fez (1) 1
flp-frt (1) 1
fmri (1) 1
functional laterality (1) 1
g2019s mutation (1) 1
gaucher cell (1) 1
gaucher disease - diagnosis (1) 1
gaucher disease - etiology (1) 1
gaucher disease - pathology (1) 1
gba mutations (1) 1
gba rare variants (1) 1
gba rare variants, gene-based analysis (1) 1
gender (1) 1
gender differences (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Brain Structure and Function, ISSN 1863-2653, 2017, Volume 222, Issue 3, pp. 1207 - 1218
Journal Article
Journal Article
Molecular Neurodegeneration, ISSN 1750-1326, 2011, Volume 6, Issue 1, pp. 66 - 66
Journal Article
Current Protocols in Human Genetics, ISSN 1934-8266, 2014, Volume 2014, pp. 17.15.1 - 17.15.6
Gaucher Disease (GD) is a progressive lysosomal storage disorder caused by deficiency of glucocerebrosidase (GBA). The clinical phenotype follows a spectrum... 
Tandem mass spectrometry | Glucocerebrosidase | Gaucher disease | Dried blood spot | GBA | Lysosomal storage disorder | tandem mass spectrometry | Gaucher Disease | dried blood spot | lysosomal storage disorder | glucocerebrosidase | Gaucher Disease - diagnosis | Humans | Infant, Newborn
Journal Article
Neuroscience Letters, ISSN 0304-3940, 08/2016, Volume 629, pp. 160 - 164
To investigate the frequency of glucocerebrosidase ( ) mutations in a Flanders-Belgian Parkinson’s disease (PD) patient cohort and to assess genotype-phenotype... 
Glucocerebrosidase | Genotype-phenotype correlation | Parkinson’s disease | GBA
Journal Article
No results were found for your search.

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