X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (29) 29
humans (27) 27
male (23) 23
female (22) 22
cardiac & cardiovascular systems (21) 21
adult (16) 16
arrhythmia (15) 15
middle aged (14) 14
genetics (10) 10
heart (10) 10
ion channels (10) 10
mutation (10) 10
article (9) 9
sodium channels - genetics (9) 9
arrhythmias (8) 8
arrhythmias, cardiac - genetics (8) 8
genotype (8) 8
long qt syndrome (8) 8
phenotype (8) 8
animals (7) 7
electrocardiography (7) 7
gene expression (7) 7
long-qt syndrome (7) 7
abridged index medicus (6) 6
aged (6) 6
brugada syndrome (6) 6
brugada syndrome - genetics (6) 6
brugada-syndrome (6) 6
cardiology (6) 6
cardiovascular (6) 6
cardiovascular diseases (6) 6
case-control studies (6) 6
genetic predisposition to disease (6) 6
genetics & heredity (6) 6
genome-wide association study (6) 6
long qt syndrome - genetics (6) 6
mutations (6) 6
myocardium - metabolism (6) 6
polymorphism, single nucleotide (6) 6
risk factors (6) 6
st-segment elevation (6) 6
adolescent (5) 5
analysis (5) 5
cardiac arrhythmia (5) 5
cardiovascular system (5) 5
congenital, hereditary, and neonatal diseases and abnormalities (5) 5
death, sudden, cardiac - etiology (5) 5
disease (5) 5
electrophysiology (5) 5
gene (5) 5
genetic aspects (5) 5
genomes (5) 5
mice (5) 5
nav1.5 voltage-gated sodium channel (5) 5
peripheral vascular disease (5) 5
sudden cardiac death (5) 5
young adult (5) 5
atrial fibrillation - genetics (4) 4
channel (4) 4
expression (4) 4
genetic research (4) 4
haplotypes (4) 4
heart failure (4) 4
hematology (4) 4
medical colleges (4) 4
muscle proteins - genetics (4) 4
mutation, missense (4) 4
research (4) 4
sodium channels (4) 4
ventricular fibrillation - genetics (4) 4
ventricular fibrillation - physiopathology (4) 4
arrhythmias, cardiac - metabolism (3) 3
atrial-fibrillation (3) 3
bundle-branch block (3) 3
cardiac and cardiovascular systems (3) 3
cardiomyopathy (3) 3
cardiovascular disease (3) 3
cells (3) 3
child (3) 3
clinical medicine (3) 3
common variants (3) 3
death, sudden, cardiac - epidemiology (3) 3
dna mutational analysis (3) 3
genetic variation (3) 3
heart conduction system - physiopathology (3) 3
heart diseases (3) 3
heart diseases - genetics (3) 3
kardiologi (3) 3
klinisk medicin (3) 3
life sciences (3) 3
loci (3) 3
medical and health sciences (3) 3
medicin och hälsovetenskap (3) 3
medicine, research & experimental (3) 3
patch-clamp techniques (3) 3
pedigree (3) 3
physiological aspects (3) 3
polymorphism (3) 3
polymorphism, genetic (3) 3
population genetics (3) 3
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


Circulation: Cardiovascular Genetics, ISSN 1942-325X, 06/2009, Volume 2, Issue 3, pp. 270 - 278
BACKGROUND—Brugada syndrome, characterized by ST-segment elevation in the right precordial ECG leads and the development of life-threatening ventricular... 
Ion channels | Arrhythmia | Brugada syndrome | SCN3B | Protein trafficking | Ion Channel | Protein Trafficking | Brugada Syndrome | Arrhythmias
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2008, Volume 118, Issue 6, pp. 2260 - 2268
Brugada syndrome is a genetic disease associated with sudden cardiac death that is characterized by ventricular fibrillation and right precordial ST segment... 
Index Medicus | Abridged Index Medicus
Journal Article
by Arking, Dan E and Pulit, Sara L and Crotti, Lia and van der Harst, Pim and Munroe, Patricia B and Koopmann, Tamara T and Sotoodehnia, Nona and Rossin, Elizabeth J and Morley, Michael and Wang, Xinchen and Johnson, Anew D and Lundby, Alicia and Gudbjartsson, Daníel F and Noseworthy, Peter A and Eijgelsheim, Mark and Bradford, Yuki and Tarasov, Kirill V and Dörr, Marcus and Müller-Nurasyid, Martina and Lahtinen, Annukka M and Nolte, Ilja M and Smith, Albert Vernon and Bis, Joshua C and Isaacs, Aaron and Newhouse, Stephen J and Evans, Daniel S and Post, Wendy S and Waggott, Daryl and Lyytikäinen, Leo-Pekka and Hicks, Anew A and Eisele, Lewin and Ellinghaus, David and Hayward, Caroline and Navarro, Pau and Ulivi, Sheila and Tanaka, Toshiko and Tester, David J and Chatel, Stéphanie and Gustafsson, Stefan and Kumari, Meena and Morris, Richard W and Naluai, Åsa T and Padmanabhan, Sandosh and Kluttig, Alexander and Strohmer, Bernhard and Panayiotou, Anie G and Torres, Maria and Knoflach, Michael and Hubacek, Jaroslav A and Slowikowski, Kamil and Raychaudhuri, Soumya and Kumar, Runjun D and Harris, Tamara B and Launer, Lenore J and Shuldiner, Alan R and Alonso, Alvaro and Bader, Joel S and Ehret, Georg and Huang, Hailiang and Kao, W. H. Linda and Strait, James B and Macfarlane, Peter W and Brown, Morris and Caulfield, Mark J and Samani, Nilesh J and Kronenberg, Florian and Willeit, Johann and Smith, J. Gustav and Greiser, Karin H and Meyer zu Schwabedissen, Henriette and Werdan, Karl and Carella, Massimo and Zelante, Leopoldo and Heckbert, Susan R and Psaty, Bruce M and Rotter, Jerome I and Kolcic, Ivana and Polašek, Ozren and Wright, Alan F and Griffin, Maura and Daly, Mark J and Arnar, David O and Hólm, Hilma and Thorsteinsdottir, Unnur and Denny, Joshua C and Roden, Dan M and Zuvich, Rebecca L and Emilsson, Valur and Plump, Anew S and Larson, Martin G and O'Donnell, Christopher J and Yin, Xiaoyan and Bobbo, Marco and D'Adamo, Adamo P and Iorio, Annamaria and Sinagra, Gianfranco and Carracedo, Angel and Cummings, Steven R and Nalls, Michael A and Jula, Antti and ... and DCCT EDIC and COGENT Consortium and eMERGE Consortium and CARe Consortium and HRGEN Consortium and DCCT/EDIC and Högskolan Dalarna and Akademin Utbildning, hälsa och samhälle and Medicinsk vetenskap
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 8, pp. 826 - 836
Journal Article
Heart Rhythm, ISSN 1547-5271, 2010, Volume 7, Issue 1, pp. 33 - 46
Journal Article
Journal of clinical investigation, ISSN 0021-9738, 2014, Volume 124, Issue 4, pp. 1844 - 1852
Journal Article
The Journal of Clinical Investigation, ISSN 0021-9738, 06/2008, Volume 118, Issue 6, pp. 2260 - 2268
Brugada syndrome is a genetic disease associated with sudden cardiac death that is characterized by ventricular fibrillation and right precordial ST segment... 
MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | SCN5A MUTATION | BETA-1 SUBUNIT | FUNCTIONAL EXPRESSION | EXTRACELLULAR DOMAIN | XENOPUS OOCYTES | LONG-QT SYNDROME | FEBRILE SEIZURES | ST-SEGMENT ELEVATION | BETA SUBUNIT
Journal Article
Heart Rhythm, ISSN 1547-5271, 2009, Volume 6, Issue 3, pp. 341 - 348
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 03/2019, Volume 73, Issue 9, pp. 1950 - 1950
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 2014, Volume 9, Issue 5, pp. e97380 - e97380
Journal Article
European Heart Journal, ISSN 0195-668X, 11/2018, Volume 39, Issue 44, pp. 3932 - 3944
Abstract Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is characterized by right ventricular myocardial replacement and life-threatening... 
Autoantibody | Biomarker | Arrhythmogenic right ventricular cardiomyopathy | Boxer dog | Human desmoglein-2 | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | CATENIN | PLAKOPHILIN-2 | PLAKOGLOBIN CAUSES | GENE | SUDDEN CARDIAC DEATH | DESMOGLEIN-2 | MUTATIONS | BINDING | CELL
Journal Article
Journal Article
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 7, pp. 822 - 824
Journal Article