X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (335) 335
Publication (40) 40
Patent (16) 16
Book / eBook (11) 11
Book Chapter (8) 8
Conference Proceeding (4) 4
Book Review (2) 2
Web Resource (2) 2
Reference (1) 1
Report (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (191) 191
index medicus (130) 130
male (118) 118
female (117) 117
infant (94) 94
genetics & heredity (91) 91
mutation (83) 83
pediatrics (77) 77
child, preschool (76) 76
child (67) 67
infant, newborn (66) 66
adolescent (48) 48
diagnosis (44) 44
endocrinology & metabolism (44) 44
medicine, research & experimental (38) 38
medicine & public health (36) 36
genetics (35) 35
mutations (35) 35
research (35) 35
children (33) 33
genetic aspects (33) 33
hypoglycemia (33) 33
metabolic diseases (33) 33
human genetics (31) 31
phenotype (31) 31
adult (30) 30
retrospective studies (26) 26
metabolism (25) 25
analysis (24) 24
internal medicine (24) 24
life sciences (24) 24
physiological aspects (24) 24
biochemistry, general (23) 23
enzymes (23) 23
infancy (23) 23
magnetic resonance imaging (23) 23
clinical neurology (22) 22
gene (22) 22
patients (21) 21
molecular sequence data (20) 20
young adult (20) 20
expression (19) 19
gene mutations (19) 19
medicine (18) 18
pancreatectomy (18) 18
animals (17) 17
deficiency (17) 17
disorders (17) 17
dna mutational analysis (17) 17
medical research (17) 17
amino acid sequence (16) 16
familial hyperinsulinism (16) 16
genes (16) 16
human necessities (16) 16
hygiene (16) 16
hyperinsulinism - genetics (16) 16
medical or veterinary science (16) 16
mutation - genetics (16) 16
pedigree (16) 16
preparations for medical, dental, or toilet purposes (16) 16
abridged index medicus (15) 15
base sequence (15) 15
care and treatment (15) 15
fibroblasts (15) 15
genetic disorders (15) 15
glycosylation (15) 15
infants (15) 15
medicine, experimental (15) 15
mitochondrial dna (15) 15
article (14) 14
biochemistry & molecular biology (14) 14
brain - pathology (14) 14
disease (14) 14
fatty acids (14) 14
insulin (14) 14
congenital hyperinsulinism (13) 13
congenital hyperinsulinism - genetics (13) 13
health aspects (13) 13
hypoglycemia - genetics (13) 13
mitochondria (13) 13
proteins (13) 13
sulfonylurea receptors (13) 13
brain (12) 12
focal adenomatous hyperplasia (12) 12
glucose (12) 12
hyperinsulinism (12) 12
hypoglycemia - etiology (12) 12
management (12) 12
middle aged (12) 12
mutation, missense (12) 12
neurology (12) 12
pharmacology (12) 12
receptors, drug - genetics (12) 12
rhabdomyolysis (12) 12
specific therapeutic activity of chemical compounds ormedicinal preparations (12) 12
syndrome (12) 12
follow-up studies (11) 11
genetic research (11) 11
hyperinsulinism - complications (11) 11
metabolic disorders (11) 11
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
UTL at Downsview - May be requested (4) 4
Robarts - Stacks (3) 3
Online Resources - Online (2) 2
Pontifical Inst. Mediaeval Studies - Library use only (2) 2
Art - Library use only (1) 1
Gerstein Science - Stacks (1) 1
Royal Ontario Museum - Rare Book (1) 1
Royal Ontario Museum - Stacks (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (336) 336
French (45) 45
German (3) 3
Spanish (3) 3
Russian (2) 2
Portuguese (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


02/2012, ISBN 9782817800455, 478
Cet ouvrage très novateur, consacré des maladies métaboliques, propose une conduite à tenir, très précise, face à une situation métabolique donnée. En effet,... 
Metabolism | Disorders
eBook
Medecine Therapeutique Pediatrie, ISSN 1286-5494, 07/2013, Volume 16, Issue 3, pp. 238 - 251
Journal Article
2013, ISBN 281780046X
Le traitement des maladies héréditaires du métabolisme est essentiel à connaître car, rapidement instauré, il peut sauver un enfant ou un adulte. Cet ouvrage... 
Medicine | Neurology | Pediatrics | Metabolic diseases | Critical care medicine
Web Resource
Bulletin de l'Academie Nationale de Medecine, ISSN 0001-4079, 01/2009, Volume 193, Issue 1, pp. 19 - 43
Journal Article
Bulletin de l'Academie Nationale de Medecine, ISSN 0001-4079, 01/2008, Volume 192, Issue 1, pp. 59 - 72
Journal Article
Journal of Thrombosis and Haemostasis, ISSN 1538-7933, 11/2019, Volume 17, Issue 11, pp. 1798 - 1807
Background Congenital disorders of glycosylation are rare inherited diseases affecting many different proteins. The lack of glycosylation notably affects the... 
congenital disorder of glycosylation | coagulation disorder | thrombin generation assay | Phenotypes | Congenital diseases | Coagulation | Thrombin | Protein C | Glycosylation | Antithrombin | Thrombosis | Hereditary diseases | Coagulation factors | Proteins | Genotype & phenotype | Protein S | Thrombomodulin
Journal Article
M/S : médecine sciences, ISSN 0767-0974, 11/2005, Volume 21, Issue 11, pp. 981 - 986
Les maladies héréditaires du métabolisme ont acquis une place de plus en plus importante dans la pathologie pédiatrique. Leur nombre ne cesse d’augmenter au... 
Journal Article
2013, ISBN 9782817800455
Cet ouvrage tres novateur, consacre des maladies metaboliques, propose une conduite a tenir, tres precise, face a une situation metabolique donnee. En effet,... 
Pre-clinical Medicine: Basic Sciences
eBook
Anti-Cancer Drugs, ISSN 0959-4973, 03/2019, Volume 30, Issue 3, pp. 313 - 317
For several decades, 5-Fluorouracil (5-FU) has been the backbone of many chemotherapy regimens for various tumor types. Its most common side effects are... 
5-fluorouracil | metabolomic disease | ONCOLOGY | UREA CYCLE DISORDERS | PHARMACOLOGY & PHARMACY | cancer | INFUSION | hyperammonemic encephalopathy | Krebs cycle
Journal Article
Pediatric Research, ISSN 0031-3998, 02/2019, Volume 85, Issue 3, pp. 384 - 389
BACKGROUND: Congenital disorders of glycosylation (CDG) includes ALG8 deficiency, a protein N-glycosylation defect with a broad clinical spectrum. If most of... 
VISUALIZATION | WIDESPREAD | SYSTEM | CONGENITAL DISORDERS | PEDIATRICS | MESSENGER-RNA DECAY | GLYCOSYLATION
Journal Article
M/S : médecine sciences, ISSN 0767-0974, 2003, Volume 19, Issue 5, pp. 527 - 528
Journal Article
Journal Article
The Journal of clinical endocrinology and metabolism, ISSN 0021-972X, 08/2017, Volume 102, Issue 8, p. 2914
Journal Article
Journal of Pediatrics, ISSN 0022-3476, 05/2011, Volume 158, Issue 5, p. 867
Journal Article
BMJ Open, ISSN 2044-6055, 11/2019, Volume 9, Issue 11, p. e032498
ObjectiveIn France, immigrants with chronic diseases encounter numerous difficulties in gaining access to care and then in its initiation and organisation,... 
Qualitative research | Social sciences | Professionals | Mental health | Patients | Mediation | Multiculturalism & pluralism | Mediators | Human immunodeficiency virus--HIV | Palliative care | Teams | Health care access | Internet | Psychiatry | Culture | Chronic illnesses
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.