X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (69) 69
index medicus (41) 41
adult (34) 34
enzyme replacement therapy (34) 34
female (33) 33
male (32) 32
middle aged (31) 31
gaucher disease - drug therapy (25) 25
gaucher disease (22) 22
hematology (21) 21
imiglucerase (19) 19
adolescent (18) 18
child (18) 18
diagnosis (18) 18
aged (17) 17
glucosylceramidase - therapeutic use (17) 17
gaucher disease - complications (16) 16
gaucher disease - genetics (15) 15
gaucher disease - diagnosis (14) 14
genetics & heredity (14) 14
glucocerebrosidase (14) 14
registries (14) 14
child, preschool (13) 13
young adult (13) 13
enzymes (12) 12
gaucher's disease (12) 12
gaucher disease - epidemiology (11) 11
splenectomy (11) 11
medicine, general & internal (10) 10
phenotype (10) 10
registry (10) 10
type-1 (10) 10
article (9) 9
cancer (9) 9
health aspects (9) 9
aged, 80 and over (8) 8
endocrinology & metabolism (8) 8
enzyme replacement therapy - methods (8) 8
medical research (8) 8
medicine, experimental (8) 8
medicine, research & experimental (8) 8
ophthalmology (8) 8
prevalence (8) 8
recombinant proteins - therapeutic use (8) 8
biopharmaceutics (7) 7
children (7) 7
follow-up studies (7) 7
gaucher disease - pathology (7) 7
genetics (7) 7
genotype (7) 7
glucosylceramidase - administration & dosage (7) 7
infant (7) 7
quality of life (7) 7
reproducibility of results (7) 7
research (7) 7
treatment outcome (7) 7
usage (7) 7
adults (6) 6
analysis (6) 6
care and treatment (6) 6
efficacy (6) 6
glucosylceramidase - genetics (6) 6
macrophage-targeted glucocerebrosidase (6) 6
mutation (6) 6
pediatrics (6) 6
risk factors (6) 6
skeletal manifestations (6) 6
disease progression (5) 5
experience (5) 5
gaucher disease - therapy (5) 5
history, 20th century (5) 5
history, 21st century (5) 5
incidence (5) 5
manifestations (5) 5
medicine (5) 5
pulmonary-hypertension (5) 5
retrospective studies (5) 5
tomography, optical coherence - methods (5) 5
velaglucerase alpha (5) 5
abnormalities (4) 4
animals (4) 4
biochemistry, general (4) 4
bone-disease (4) 4
disease (4) 4
gaucher disease - blood (4) 4
gaucher disease - enzymology (4) 4
glaucoma (4) 4
glucosylceramidase - adverse effects (4) 4
human genetics (4) 4
infant, newborn (4) 4
internal medicine (4) 4
involvement (4) 4
magnetic resonance imaging (4) 4
management (4) 4
medical colleges (4) 4
mutations (4) 4
patient outcomes (4) 4
pharmacology (4) 4
platelet count (4) 4
recombinant proteins - administration & dosage (4) 4
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (2) 2
Robarts - Stacks (2) 2
Art - Reference (1) 1
Trinity College (John W Graham) - Reference (1) 1
UTL at Downsview - May be requested (1) 1
Victoria University E.J. Pratt - Reference (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 2403 - 2403
Abstract Type 1 Gaucher disease (GD1) is a rare, autosomal recessive disorder. Deficient lysosomal glucocerebrosidase activity causes accumulation of... 
Journal Article
American Journal of Hematology, ISSN 0361-8609, 07/2015, Volume 90, Issue 1, pp. S2 - S5
Journal Article
Blood, ISSN 0006-4971, 04/2017, Volume 129, Issue 17, pp. 2337 - 2338
In this issue of Blood, Cox et al show that 157 adult patients with type 1 (nonneuronopathic) Gaucher disease (GD), whose initial signs and symptoms improved... 
HEMATOLOGY | GLUCOCEREBROSIDASE
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2019, Volume 126, Issue 2, pp. S151 - S151
Journal Article
Critical Reviews in Oncogenesis, ISSN 0893-9675, 2013, Volume 18, Issue 3, pp. 163 - 175
Gaucher disease (GD) is an inherited error of metabolism due to a deficiency of glucocerebrosidase. This leads to excessive storage of glucocerebroside in the... 
Substrate reduction | Glucocerebroside | Gaucher | Glucocerebrosidase | Enzyme replacement | History, 21st Century | History, 20th Century | Humans | Gaucher Disease - etiology | Gaucher Disease - epidemiology | History, 19th Century | Gaucher Disease - therapy | Gaucher Disease - diagnosis | Gaucher Disease - history
Journal Article
Pediatric endocrinology reviews : PER, ISSN 1565-4753, 2013, Volume 11, pp. 77 - 90
For more than 20 years, "enzyme replacement therapy" (ERT) has been the prevalent treatment approach for lysosomal storage disorders (LSDs). Unfortunately,... 
Enzyme Inhibitors - administration & dosage | Enzyme Replacement Therapy - methods | Molecular Weight | Administration, Oral | Lysosomal Storage Diseases - drug therapy | Enzyme Inhibitors - chemistry | Humans
Journal Article
Journal Article
Journal of Bone and Mineral Research, ISSN 0884-0431, 06/2019, Volume 34, Issue 6, pp. 996 - 1013
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 2008, Volume 93, Issue 2, pp. 41 - 41
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 10/2019
Journal Article
Blood, ISSN 0006-4971, 11/2019, Volume 134, Issue Supplement_1, pp. 4859 - 4859
INTRODUCTION: Gaucher disease type 1 (GD1) is caused by hereditary deficiency in activity of lysosomal acid β-glucosidase and lysosomal dysfunction due to... 
Journal Article