UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.

Search Articles

X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
science & technology (52) 52
life sciences & biomedicine (49) 49
humans (45) 45
male (27) 27
female (25) 25
genetics & heredity (20) 20
animals (19) 19
child (17) 17
adult (16) 16
cardiac & cardiovascular systems (14) 14
cardiovascular system & cardiology (14) 14
jacobsen syndrome (13) 13
child, preschool (12) 12
mice (12) 12
adolescent (11) 11
infant (11) 11
congenital heart disease (10) 10
abridged index medicus (9) 9
infant, newborn (9) 9
heart (8) 8
jacobsen distal 11q deletion syndrome - genetics (8) 8
cardiology (7) 7
chromosomes, human, pair 11 - genetics (7) 7
hypoplastic left heart syndrome - genetics (7) 7
pediatrics (7) 7
young adult (7) 7
analysis (6) 6
chromosome deletion (6) 6
gene deletion (6) 6
genetic disorders (6) 6
heart defects, congenital - genetics (6) 6
mice, knockout (6) 6
mutation (6) 6
phenotype (6) 6
biochemistry & molecular biology (5) 5
cardiovascular disease (5) 5
genetics (5) 5
hypoplastic left heart syndrome (5) 5
syndrome (5) 5
chromosomes, human, pair 11 (4) 4
defects (4) 4
disease models, animal (4) 4
genes (4) 4
internal medicine (4) 4
mice, inbred c57bl (4) 4
risk factors (4) 4
treatment outcome (4) 4
aged (3) 3
atenolol - therapeutic use (3) 3
base sequence (3) 3
cardiology and cardiovascular medicine (3) 3
cardiovascular (3) 3
cardiovascular malformation (3) 3
children & youth (3) 3
chromosome 11 (3) 3
chromosome disorders - genetics (3) 3
chromosome mapping (3) 3
cohort studies (3) 3
echocardiography - methods (3) 3
etiology (3) 3
genetic aspects (3) 3
genomics (3) 3
heart diseases (3) 3
in situ hybridization, fluorescence (3) 3
jacobsen distal 11q deletion syndrome - complications (3) 3
jacobsen distal 11q deletion syndrome - diagnosis (3) 3
losartan - therapeutic use (3) 3
marfan syndrome (3) 3
marfan syndrome - drug therapy (3) 3
medicine & public health (3) 3
middle aged (3) 3
myocardium - pathology (3) 3
pedigree (3) 3
proto-oncogene protein c-ets-1 - genetics (3) 3
retrospective studies (3) 3
11q terminal deletion disorder (2) 2
abnormalities, multiple - genetics (2) 2
abnormalities, multiple - pathology (2) 2
aged, 80 and over (2) 2
antihypertensive agents - therapeutic use (2) 2
aorta (2) 2
aorta - surgery (2) 2
aortic dilation (2) 2
aortic valve - abnormalities (2) 2
aortic valve insufficiency (2) 2
autism (2) 2
cardiac and cardiovascular systems (2) 2
cardiovascular abnormalities - genetics (2) 2
cardiovascular system (2) 2
care and treatment (2) 2
cell adhesion molecules - genetics (2) 2
cell proliferation (2) 2
chaotic atrial rhythm (2) 2
children (2) 2
clinical medicine (2) 2
comparative analysis (2) 2
congenital heart defect (2) 2
coronary artery disease (2) 2
coronary vessels (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The New England journal of medicine, ISSN 1533-4406, 11/2014, Volume 371, Issue 22, pp. 2061 - 2071
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 06/2003, Volume 41, Issue 11, pp. 2072 - 2076
Journal Article
Pediatric cardiology, ISSN 0172-0643, 2018, Volume 39, Issue 7, pp. 1453 - 1461
... for Aortic Surgery in Marfan Syndrome Arvind Hoskoppal 1 · Shaji Menon 1 · Felicia Trachtenberg 2 · Kristin M. Burns 3 · Julie De Backer 4 · Bruce D. Gelb 5 · Marie... 
Medicine & Public Health | Cardiac Surgery | Referral for aortic surgery | Vascular Surgery | Cardiology | Marfan syndrome | Predictors | Aortic root dilation | Cardiac & Cardiovascular Systems | Pediatrics | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Risk Assessment - methods | Humans | Marfan Syndrome - surgery | Echocardiography - methods | Child, Preschool | Vascular Surgical Procedures - statistics & numerical data | Infant | Male | Young Adult | Angiotensin II Type 1 Receptor Blockers | Marfan Syndrome - drug therapy | Dilatation | Adult | Female | Marfan Syndrome - complications | Child | Aortic Diseases - epidemiology | Risk Factors | Referral and Consultation - statistics & numerical data | Antihypertensive Agents - therapeutic use | Aorta - pathology | Aortic Diseases - surgery | Atenolol - therapeutic use | Aorta - surgery | Adolescent | Losartan - therapeutic use | ROC Curve | Aortic Diseases - etiology | Index Medicus | Medical and Health Sciences | Medicin och hälsovetenskap | Pediatrik | Aortic Diseases/epidemiology | Marfan Syndrome/complications | Klinisk medicin | Kardiologi | Echocardiography/methods | Aorta/pathology | Risk Assessment/methods | Losartan/therapeutic use | Vascular Surgical Procedures/statistics & numerical data | Antihypertensive Agents/therapeutic use | Clinical Medicine | Cardiac and Cardiovascular Systems | Referral and Consultation/statistics & numerical data | Atenolol/therapeutic use
Journal Article
Journal Article
Nature genetics, ISSN 1061-4036, 05/2017, Volume 49, Issue 7, pp. 1152 - 1159
Journal Article
Nature (London), ISSN 1476-4687, 07/2005, Volume 437, Issue 7056, pp. 270 - 274
Journal Article