X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (28) 28
humans (22) 22
mutation (13) 13
female (12) 12
genetics (11) 11
genetics & heredity (11) 11
male (11) 11
pedigree (11) 11
adult (10) 10
chromosome mapping (9) 9
genes (9) 9
genetic aspects (9) 9
animals (8) 8
clinical neurology (8) 8
consanguinity (8) 8
morocco (8) 8
mutations (8) 8
phenotype (8) 8
research (8) 8
neurosciences (7) 7
parkinson's disease (7) 7
adolescent (6) 6
amino acid sequence (6) 6
gene (6) 6
hsp90 heat-shock proteins - metabolism (6) 6
protein (6) 6
biochemistry & molecular biology (5) 5
child (5) 5
disease (5) 5
genetic research (5) 5
genotype (5) 5
health aspects (5) 5
hsp90 heat-shock proteins - genetics (5) 5
lod score (5) 5
middle aged (5) 5
research article (5) 5
spastic paraplegia, hereditary - genetics (5) 5
age of onset (4) 4
analysis (4) 4
article (4) 4
base sequence (4) 4
charcot-marie-tooth disease - genetics (4) 4
chickens (4) 4
gene mutations (4) 4
genetic disorders (4) 4
genetic linkage (4) 4
haplotypes (4) 4
heat shock proteins (4) 4
homozygote (4) 4
hsp90 heat-shock proteins - chemistry (4) 4
mice (4) 4
microsatellite repeats (4) 4
molecular sequence data (4) 4
moroccan patients (4) 4
multidisciplinary sciences (4) 4
nervous system diseases (4) 4
neurology (4) 4
paraplegia (4) 4
physiological aspects (4) 4
recombinant fusion proteins - metabolism (4) 4
sequence analysis, dna (4) 4
age (3) 3
axons - physiology (3) 3
binding sites (3) 3
charcot-marie-tooth disease (3) 3
child, preschool (3) 3
dna sequencing (3) 3
epidemiology (3) 3
estrogen-receptor (3) 3
genes, recessive (3) 3
genomics (3) 3
hereditary spastic paraplegia (3) 3
identification (3) 3
life sciences (3) 3
linkage analysis (3) 3
locus (3) 3
neurodegeneration (3) 3
neurology. diseases of the nervous system (3) 3
neurons and cognition (3) 3
neuropathy (3) 3
paralysis (3) 3
patients (3) 3
progesterone-receptor (3) 3
protein binding (3) 3
proteins (3) 3
quality of life (3) 3
receptors (3) 3
recombinant fusion proteins - chemistry (3) 3
seizures (3) 3
young adult (3) 3
adenosine triphosphate - metabolism (2) 2
amino acids (2) 2
antibodies (2) 2
article subject (2) 2
atp binding (2) 2
autosomal recessive form (2) 2
axonal form (2) 2
biochemistry (2) 2
biological sciences (2) 2
biomedicine (2) 2
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 American Journal of Human Genetics, ISSN 0002-9297, 12/2012, Volume 91, Issue 6, pp. 1051 - 1064
Journal Article
Journal Article
Science, ISSN 0036-8075, 2014, Volume 343, Issue 6170, pp. 506 - 511
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 04/2018, Volume 9
BackgroundNon-motor symptoms (NMSs) are a real burden in Parkinson’s disease (PD). They may appear in early pre-symptomatic stage as well as throughout the... 
Moroccan patients | quality of life | non-motor symptoms | motor symptoms | Parkinson’s disease
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 11/2000, Volume 97, Issue 23, pp. 12524 - 12529
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 04/2018, Volume 9, pp. 170 - 170
Background: Non-motor symptoms (NMSs) are a real burden in Parkinson's disease (PD). They may appear in early pre-symptomatic stage as well as throughout the... 
Moroccan patients | Non-motor symptoms | Parkinson's disease | Motor symptoms | Quality of life | DEPRESSION | OLFACTORY DYSFUNCTION | DAYTIME SLEEPINESS | AUTONOMIC DYSFUNCTION | DETERMINANTS | FATIGUE | DISORDERS | MONTGOMERY-ASBERG | PREVALENCE | non-motor symptoms | NEUROSCIENCES | CLINICAL NEUROLOGY | motor symptoms | quality of life | EPIDEMIOLOGY | Research | Health aspects
Journal Article
Parkinson's Disease, ISSN 2090-8083, 2017, Volume 2017, pp. 2412486 - 2412486
Background. The LRRK2 G2019S mutation is the most common genetic determinant of Parkinson's disease (PD) identified to date. This mutation, reported in both... 
PENETRANCE | GENE | NORTH-AFRICAN | FAMILIES | FREQUENCY | EARLY-ONSET | PHENOTYPE | ASHKENAZI JEWS | CLINICAL NEUROLOGY | Genetic aspects | Parkinson's disease | Gene mutations | Health aspects | Statistics | Risk factors
Journal Article