X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2164) 2164
Book Review (415) 415
Publication (197) 197
Book Chapter (33) 33
Conference Proceeding (8) 8
Dissertation (7) 7
Book / eBook (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1629) 1629
humans (1416) 1416
glucocerebrosidase (1067) 1067
gaucher disease (689) 689
male (562) 562
female (555) 555
glucosylceramidase - genetics (485) 485
animals (469) 469
mutation (449) 449
gaucher disease - genetics (444) 444
enzyme replacement therapy (386) 386
genetics & heredity (385) 385
biochemistry & molecular biology (370) 370
adult (357) 357
parkinson's disease (354) 354
enzymes (337) 337
middle aged (327) 327
gaucher-disease (324) 324
glucocerebrosidase mutations (283) 283
gaucher's disease (275) 275
glucosylceramidase - metabolism (269) 269
clinical neurology (268) 268
mice (265) 265
alpha-synuclein (262) 262
neurosciences (257) 257
gaucher disease - drug therapy (251) 251
hematology (236) 236
phenotype (230) 230
aged (229) 229
gaucher disease - enzymology (218) 218
mutations (213) 213
genotype (212) 212
parkinson disease - genetics (212) 212
medicine, research & experimental (210) 210
glucocerebrosidase gene (209) 209
child (203) 203
glucosylceramidase - therapeutic use (196) 196
adolescent (194) 194
gaucher disease - pathology (182) 182
macrophage-targeted glucocerebrosidase (168) 168
gaucher disease - diagnosis (163) 163
gene (163) 163
analysis (161) 161
beta-glucocerebrosidase (155) 155
deficiency (155) 155
child, preschool (154) 154
type-1 (151) 151
abridged index medicus (145) 145
genetic aspects (145) 145
identification (145) 145
gaucher disease - complications (142) 142
acid beta-glucosidase (141) 141
pediatrics (139) 139
genetics (138) 138
parkinsons-disease (136) 136
diagnosis (135) 135
risk factors (134) 134
alleles (128) 128
disease (127) 127
gba (125) 125
article (124) 124
gaucher disease - therapy (124) 124
human glucocerebrosidase gene (123) 123
replacement therapy (122) 122
cell biology (118) 118
expression (118) 118
hydrolases (117) 117
cells, cultured (115) 115
dementia (115) 115
cells (113) 113
gaucher disease - metabolism (110) 110
mutation - genetics (109) 109
research (108) 108
infant (105) 105
glucosylceramidase (104) 104
molecular sequence data (104) 104
biotechnology & applied microbiology (100) 100
fibroblasts (99) 99
medicine, general & internal (99) 99
dna mutational analysis (97) 97
lysosomal storage disorders (96) 96
endocrinology & metabolism (94) 94
beta-glucosidase (92) 92
parkinson disease (92) 92
base sequence (90) 90
mouse model (89) 89
proteins (89) 89
pathology (88) 88
therapy (88) 88
imiglucerase (87) 87
polymerase chain reaction (87) 87
disease models, animal (86) 86
genes (86) 86
health aspects (86) 86
aged, 80 and over (85) 85
glucosylceramidase - deficiency (84) 84
lysosomes - metabolism (84) 84
neurology (84) 84
cell line (83) 83
medical research (83) 83
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2106) 2106
French (30) 30
Spanish (19) 19
German (18) 18
Italian (5) 5
Polish (3) 3
Portuguese (3) 3
Russian (3) 3
Czech (2) 2
Japanese (2) 2
Arabic (1) 1
Catalan (1) 1
Chinese (1) 1
Hungarian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Movement Disorders, ISSN 0885-3185, 10/2017, Volume 32, Issue 10, pp. 1423 - 1431
Journal Article
Journal Article
Parkinsonism & related disorders, ISSN 1353-8020, 04/2019
Mutations in the glucocerebrosidase (GBA) gene are strongly associated with REM sleep behavior disorder (RBD). It is unclear whether GBA mutations might affect... 
Journal Article
Journal Article