X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (62) 62
clinical neurology (50) 50
male (45) 45
index medicus (44) 44
female (40) 40
middle aged (40) 40
aged (34) 34
adult (30) 30
neurosciences (27) 27
mutation (17) 17
pedigree (16) 16
spastic paraplegia, hereditary - genetics (15) 15
genetics & heredity (14) 14
hereditary spastic paraplegia (14) 14
life sciences (14) 14
neurology (14) 14
parkinson's disease (14) 14
aged, 80 and over (13) 13
gene (12) 12
adolescent (11) 11
genetic aspects (11) 11
genetics (11) 11
phenotype (11) 11
genotype (10) 10
mutation - genetics (10) 10
neurons and cognition (10) 10
young adult (10) 10
dna mutational analysis (9) 9
parkinson disease - genetics (9) 9
risk (9) 9
[sdv.neu]life sciences [q-bio]/neurons and cognition [q-bio.nc] (8) 8
age (8) 8
age of onset (8) 8
care and treatment (8) 8
essential tremor (8) 8
family (8) 8
psychiatry (8) 8
research (8) 8
abridged index medicus (7) 7
analysis (7) 7
article (7) 7
essential tremor - genetics (7) 7
gene mutations (7) 7
mutation, missense (7) 7
parkinson disease - diagnosis (7) 7
risk factors (7) 7
biochemistry & molecular biology (6) 6
case-control studies (6) 6
disease (6) 6
disease progression (6) 6
family health (6) 6
heat shock proteins (6) 6
heterozygote (6) 6
huntington's disease (6) 6
mesh: humans (6) 6
movement disorders (6) 6
parkinsons-disease (6) 6
protein (6) 6
tremor (6) 6
biomedicine (5) 5
cancer (5) 5
chromosome mapping (5) 5
dementia (5) 5
genetic disorders (5) 5
genetic heterogeneity (5) 5
germany (5) 5
human genetics (5) 5
locus (5) 5
medicine & public health (5) 5
membrane proteins - genetics (5) 5
mesh: female (5) 5
mesh: male (5) 5
molecular medicine (5) 5
mutations (5) 5
onset (5) 5
paralysis, spastic (5) 5
parkinsons disease (5) 5
polymorphism, single nucleotide (5) 5
prevalence (5) 5
scale (5) 5
spastic paraplegia, hereditary - diagnosis (5) 5
[ sdv.neu ] life sciences [q-bio]/neurons and cognition [q-bio.nc] (4) 4
amyotrophic-lateral-sclerosis (4) 4
antiparkinson agents - adverse effects (4) 4
antiparkinson agents - therapeutic use (4) 4
cohort studies (4) 4
consanguinity (4) 4
development and progression (4) 4
diagnosis (4) 4
dopamine (4) 4
form (4) 4
france (4) 4
frequent cause (4) 4
genes, recessive (4) 4
genetic variation (4) 4
haplotypes (4) 4
health aspects (4) 4
identification (4) 4
linkage (4) 4
magnetic resonance imaging - methods (4) 4
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Neurology, ISSN 0340-5354, 9/2015, Volume 262, Issue 9, pp. 2124 - 2134
Journal Article
DNP - Der Neurologe & Psychiater, ISSN 1616-2455, 02/2019, Volume 20, Issue 1, pp. 12 - 13
Journal Article
DNP - Der Neurologe & Psychiater, ISSN 1616-2455, 02/2019, Volume 20, Issue 1, pp. 13 - 14
Journal Article
InFo Neurologie & Psychiatrie, ISSN 1437-062X, 05/2018, Volume 20, Issue 5, pp. 16 - 16
Journal Article
DNP - Der Neurologe & Psychiater, ISSN 1616-2455, 12/2017, Volume 18, Issue 11-12, pp. 33 - 36
Journal Article
Der Nervenarzt, ISSN 0028-2804, 2/2019, Volume 90, Issue 2, pp. 197 - 210
Seltene genetische Bewegungsstörungen sind eine heterogene Gruppe von Erkrankungen. Durch die Entwicklungen in der molekulargenetischen Diagnostik konnte die... 
Molecular diagnostics | Psychotherapy | Molekulargenetische Diagnostik | Neurosurgery | Medicine/Public Health, general | Neurology | Medicine & Public Health | Genetische Parkinson-Syndrome | Dystonien | Genetic Parkinson syndromes | Differenzialdiagnostik | Dystonia | Differential diagnostics | Psychiatry | Next Generation Sequencing
Journal Article
Der Nervenarzt, ISSN 0028-2804, 02/2019, Volume 90, Issue 2, p. 197
Seltene genetische Bewegungsstorungen sind eine heterogene Gruppe von Erkrankungen. Durch die Entwicklungen in der molekulargenetischen Diagnostik konnte die... 
Tremor | Genetic aspects
Journal Article
DNP - Der Neurologe & Psychiater, ISSN 1616-2455, 03/2017, Volume 18, Issue 3, pp. 18 - 19
Journal Article
DNP - Der Neurologe & Psychiater, ISSN 1616-2455, 03/2017, Volume 18, Issue 3, pp. 21 - 21
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 08/2006, Volume 355, Issue 9, pp. 896 - 908
Journal Article
Acta neuropathologica, ISSN 0001-6322, 2017, Volume 133, Issue 4, pp. 535 - 545
Journal Article
Movement Disorders, ISSN 0885-3185, 10/2016, Volume 31, Issue 10, pp. 1560 - 1566
Journal Article
NERVENARZT, ISSN 0028-2804, 02/2019, Volume 90, Issue 2, pp. 197 - 210
Rare genetic movement disorders are a heterogeneous group of diseases. The causes of many of these rare movement disorders could be resolved due to the... 
LRRK2 G2019S | Molecular diagnostics | HEREDITARY SPASTIC PARAPLEGIA | GENOTYPE | PSYCHIATRY | PHENOTYPE | SEQUENCE VARIANTS | Next generation sequencing | CLINICAL NEUROLOGY | SPG7 MUTATIONS | Genetic Parkinson syndromes | Dystonia | Differential diagnostics | DEEP BRAIN-STIMULATION | ASSOCIATION | PARKINSONS-DISEASE
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 4/2017, Volume 133, Issue 4, pp. 535 - 545
Phosphorylated alpha-synuclein (p-alpha-syn) deposits, one of the neuropathological hallmarks of Parkinson’s disease (PD), have recently been detected in... 
Pathology | Neurosciences | Medicine & Public Health | REM sleep behaviour disorder | Skin biopsy | FP-CIT-SPECT | Parkinson’s disease | Alpha-synuclein | Original Paper
Journal Article