X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (449) 449
Book Review (161) 161
Book Chapter (45) 45
Publication (31) 31
Book / eBook (7) 7
Data Set (1) 1
Dissertation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (357) 357
humans (342) 342
clinical neurology (201) 201
neurosciences (172) 172
parkinson's disease (172) 172
mutation (159) 159
parkinson disease - genetics (156) 156
female (147) 147
male (140) 140
autosomal-dominant parkinsonism (132) 132
adult (114) 114
middle aged (105) 105
alpha-synuclein (94) 94
animals (88) 88
neurology (84) 84
genetic aspects (83) 83
gene (82) 82
disease (81) 81
genetics (78) 78
aged (73) 73
mutations (71) 71
early-onset parkinsonism (69) 69
leucine-rich repeat serine-threonine protein kinase-2 (68) 68
pedigree (68) 68
mutation - genetics (64) 64
protein-serine-threonine kinases - genetics (62) 62
recessive juvenile parkinsonism (61) 61
ubiquitin-protein ligases - genetics (61) 61
parkin (59) 59
parkinsonian disorders - genetics (58) 58
autosomal-dominant (55) 55
biochemistry & molecular biology (54) 54
genetics & heredity (53) 53
age of onset (51) 51
autosomal recessive juvenile parkinsonism (48) 48
phenotype (48) 48
lrrk2 (43) 43
dna mutational analysis (42) 42
pathology (42) 42
nervous system diseases (41) 41
protein kinases - genetics (41) 41
autosomal recessive (40) 40
parkinson disease - pathology (40) 40
gene mutations (39) 39
parkinson disease (39) 39
adolescent (38) 38
juvenile parkinsonism (38) 38
alpha-synuclein - genetics (37) 37
genes (37) 37
analysis (36) 36
parkinsonism (36) 36
parkinsons disease (36) 36
multiple system atrophy (35) 35
lewy bodies (34) 34
neurodegenerative diseases (34) 34
brain - pathology (32) 32
family health (32) 32
genetic predisposition to disease (32) 32
parkinson disease - metabolism (32) 32
neurodegeneration (31) 31
alpha-synuclein gene (30) 30
genetic research (30) 30
pink1 (30) 30
aged, 80 and over (29) 29
ataxia (29) 29
autosomal recessive parkinsonism (29) 29
dementia (29) 29
movement disorders (29) 29
protein deglycase dj-1 (29) 29
research (29) 29
child (28) 28
dna, mitochondrial - genetics (28) 28
early-onset (27) 27
genes, recessive (27) 27
genotype (27) 27
progressive external ophthalmoplegia (27) 27
ubiquitin-protein ligase (27) 27
diagnosis (26) 26
dystonia (26) 26
dystonic syndrome starting with focal signs or with functional dystonia (26) 26
progressive encephalomyelitis with rigidity and myoclonus (26) 26
progressive supranuclear palsy, presenting with parkinsonism (26) 26
proteins (26) 26
sca2 expansion, resulting in typical pd (26) 26
ubiquitin-protein ligases (26) 26
use of dat spect, facilitating differential diagnosis in patients with isolated tremor symptoms (26) 26
wilson's disease, autosomal recessive disorder linking to mutation of atp7b gene mapped to chromosome 13 (26) 26
constipation and smell loss, non-motor symptoms occurring in de novo pd patients (25) 25
family (25) 25
fluid-attenuated inversion recovery (25) 25
mitochondrial dna (25) 25
oncogene proteins - genetics (25) 25
urinary urgency and erectile dysfunction - common in msa (25) 25
genetic predisposition to disease - genetics (24) 24
magnetic resonance imaging (24) 24
parkinson disease - physiopathology (24) 24
proteins - genetics (23) 23
young adult (23) 23
abridged index medicus (22) 22
article (22) 22
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


2015, Sixth edition., ISBN 1608311767, xii, 576 pages
Top experts from all over the world have been brought together by the editors, to give a world of expertise on this important subject, with a strong emphasis... 
Parkinson Disease | Movement Disorders
Book
Journal Article
Neuroscience Letters, ISSN 0304-3940, 06/2016, Volume 624, pp. 100 - 104
Journal Article
Cold Spring Harbor Perspectives in Medicine, ISSN 2157-1422, 2012, Volume 2, Issue 6, pp. a008870 - a008870
Journal Article
Journal Article
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 07/2006, Volume 98, Issue 1, pp. 156 - 169
Following our identification of PTEN‐induced putative kinase 1 ( PINK1 ) gene mutations in PARK6‐linked Parkinson's disease (PD), we have recently reported... 
autosomal‐recessive juvenile parkinsonism | microtubule organizing centre | ubiquitin–proteasome system | Parkinson's disease | mitochondrial processing peptidase | Lewy body | PROTEIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | ALPHA-SYNUCLEIN | RECESSIVE PARKINSONISM | SUBSTANTIA-NIGRA | NEUROSCIENCES | ubiquitin-proteasome system | INCLUSION-BODIES | DISEASE | autosomal-recessive juvenile parkinsonism | MUTATIONS | MITOCHONDRIAL INNER MEMBRANE | LEWY BODIES | EARLY-ONSET PARKINSONISM | Protein Kinases - metabolism | Protein Kinases - genetics | Humans | Proteasome Endopeptidase Complex | Mitochondria - ultrastructure | Brain - metabolism | Stress, Physiological - chemically induced | Transfection - methods | Stress, Physiological - metabolism | Brain - ultrastructure | Cloning, Molecular - methods | Parkinson Disease - metabolism | Microscopy, Immunoelectron - methods | Cell Line | Green Fluorescent Proteins - metabolism | Blotting, Western - methods | Cricetinae | Parkinson Disease - pathology | Fluorescent Antibody Technique - methods | Enzyme Inhibitors - pharmacology | Mutant Proteins - genetics | Mitochondria - metabolism | Mutant Proteins - physiology | Parkinson Disease - genetics | Nerve Tissue Proteins - metabolism | Leupeptins - pharmacology | Animals | Cysteine Proteinase Inhibitors - pharmacology | Brain - pathology | Proteins | Enzymes | Brain | Mutation | Genes | Parkinsons disease | Index Medicus
Journal Article