X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (111) 111
andersen-tawil syndrome (101) 101
humans (98) 98
andersen-tawil-syndrome (74) 74
cardiac & cardiovascular systems (51) 51
periodic paralysis (47) 47
mutation (45) 45
potassium channels, inwardly rectifying - genetics (40) 40
animals (38) 38
kir2.1 (36) 36
female (35) 35
andersen syndrome - genetics (32) 32
male (32) 32
phenotype (30) 30
adult (28) 28
andersen–tawil syndrome (28) 28
kcnj2 (28) 28
arrhythmia (26) 26
kcnj2 mutations (26) 26
long qt syndrome (26) 26
mutations (26) 26
neurosciences (24) 24
electrocardiography (23) 23
clinical neurology (22) 22
heart (21) 21
adolescent (19) 19
channelopathies (19) 19
genetic aspects (18) 18
genotype (18) 18
ion channels (18) 18
physiology (18) 18
potassium channel (18) 18
potassium channels, inwardly rectifying - metabolism (18) 18
analysis (17) 17
child (17) 17
hypokalemic periodic paralysis (17) 17
potassium channels (17) 17
article (16) 16
andersen syndrome - physiopathology (15) 15
genetics & heredity (15) 15
sudden cardiac death (15) 15
andersen syndrome - diagnosis (14) 14
cardiovascular (14) 14
cell biology (14) 14
channelopathy (14) 14
long-qt syndrome (14) 14
mutation - genetics (13) 13
arrhythmias, cardiac - genetics (12) 12
biochemistry & molecular biology (12) 12
cardiovascular system (12) 12
channelopathies - genetics (12) 12
dna mutational analysis (12) 12
paralysis (12) 12
polymorphic ventricular-tachycardia (12) 12
potassium (12) 12
tachycardia, ventricular - genetics (12) 12
arrhythmias (11) 11
genetic predisposition to disease (11) 11
long qt syndrome - genetics (11) 11
muscle, skeletal - physiopathology (11) 11
potassium channels, inwardly rectifying - chemistry (11) 11
tachycardia (11) 11
diagnosis (10) 10
flecainide (10) 10
gene mutations (10) 10
mice (10) 10
pharmacology & pharmacy (10) 10
proteins (10) 10
risk factors (10) 10
ventricular tachycardia (10) 10
arrhythmias, cardiac - physiopathology (9) 9
cardiac arrhythmia (9) 9
diagnosis, differential (9) 9
electrophysiology (9) 9
features (9) 9
genetic disorders (9) 9
genetics (9) 9
ion channels - genetics (9) 9
kcnj2 gene (9) 9
kcnj2 mutation (9) 9
models, molecular (9) 9
molecular sequence data (9) 9
pedigree (9) 9
research (9) 9
u-wave (9) 9
amino acid sequence (8) 8
andersen syndrome - complications (8) 8
andersen‐tawil syndrome (8) 8
bidirectional ventricular tachycardia (8) 8
care and treatment (8) 8
case report (8) 8
channelopathies - physiopathology (8) 8
exercise test (8) 8
health aspects (8) 8
heart diseases (8) 8
muscles (8) 8
myocytes, cardiac - metabolism (8) 8
myotonia (8) 8
neurology (8) 8
paramyotonia-congenita (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Indian Journal of Pediatrics, ISSN 0019-5456, 2019, Volume 86, Issue 5, pp. 480 - 480
Journal Article
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, ISSN 1003-9406, 10/2018, Volume 35, Issue 5, pp. 675 - 678
Journal Article
Circulation Research, ISSN 0009-7330, 05/2018, Volume 122, Issue 11, pp. 1482 - 1484
Journal Article
Neurology international, ISSN 2035-8385, 06/2019, Volume 11, Issue 2, pp. 8180 - 8180
Andersen-Tawil syndrome (ATS) is characterized by a triad of periodic paralysis, cardiac arrhythmias and distinctive dysmorphic features. Due to its rarity and... 
literature review | Delayed diagnosed | Andersen-Tawil syndrome
Journal Article
Frontiers in Physiology, ISSN 1664-042X, 2015, Volume 6, pp. 7 - 7
Human induced pluripotent stem cell derived cardiomyocytes (hiPSC-CMs) are widely used in studying basic mechanisms of cardiac arrhythmias that are caused by... 
Kir2.1 protein | Action potentials | Inward rectifier potassium channel | Cardiac ion channelopathies | Patch clamp | Short QT syndrome 3 | KCNJ2 gene | Andersen-tawil syndrome | Action Potentials | patch clamp | cardiac ion channelopathies | inward rectifier potassium channel | Andersen-Tawil syndrome
Journal Article
JOURNAL OF GENERAL PHYSIOLOGY, ISSN 0022-1295, 07/2018, Volume 150, Issue 7, pp. 991 - 1002
Recent evidence suggests that neuronal Na+ channels (nNays) contribute to catecholamine-promoted delayed afterdepolarizations (DADs) and catecholaminergic... 
ANDERSEN-TAWIL SYNDROME | LATE SODIUM CURRENT | POLYMORPHIC VENTRICULAR-TACHYCARDIA | TORSADES-DE-POINTES | TRIGGERED ACTIVITY | PHYSIOLOGY | DRUG-INDUCED MODEL | RYANODINE RECEPTOR | MOUSE HEART | CA2+ RELEASE | NA+ CHANNELS
Journal Article
Acta Physiologica, ISSN 1748-1708, 07/2010, Volume 199, Issue 3, pp. 243 - 256
Inward rectifier currents based on KIR2.x subunits are regarded as essential components for establishing a stable and negative resting membrane potential in... 
barium | expression pattern | thyrotoxic periodic paralysis | KIR2.x | Andersen-Tawil syndrome | inward rectifier current | Inward rectifier current | Barium | 2.x | Expression pattern | Thyrotoxic periodic paralysis
Journal Article
CIRCULATION RESEARCH, ISSN 0009-7330, 05/2018, Volume 122, Issue 11, pp. 1501 - 1516
Rationale: In cardiomyocytes, Na(v)1.5 and Kir2.1 channels interact dynamically as part of membrane bound macromolecular complexes. Objective: The objective of... 
CARDIAC & CARDIOVASCULAR SYSTEMS | ANDERSEN-TAWIL-SYNDROME | action potentials | arrhythmias, cardiac | SURFACE EXPRESSION | DIFFERENTIAL DISTRIBUTION | DOMAIN-BINDING | SODIUM-CHANNEL | PLASMA-MEMBRANE | ion channels | Golgi apparatus | electrophysiology | PERIPHERAL VASCULAR DISEASE | SELECTIVE GOLGI EXPORT | HEMATOLOGY | HUMAN HEART | UP-REGULATION | POTASSIUM CHANNEL
Journal Article
Annals of Noninvasive Electrocardiology, ISSN 1082-720X, 05/2019, Volume 24, Issue 3, pp. e12624 - n/a
We report on a 44‐year‐old woman with coincidence of two genetic disorders: Andersen–Tawil syndrome and Marfan syndrome. In both, life‐threatening arrhythmias... 
thoracic aortic aneurysms and dissections | Andersen–Tawil syndrome | long QT syndrome | Marfan syndrome | CARDIAC & CARDIOVASCULAR SYSTEMS | Andersen-Tawil syndrome | MUTATION | Aneurysms | Electrocardiography | Arrhythmia | Analysis | Electrocardiogram
Journal Article
The EMBO Journal, ISSN 0261-4189, 09/2007, Volume 26, Issue 17, pp. 4005 - 4015
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 05/2018, Volume 28, Issue 5, pp. 402 - 407
Few reliable data exist on the prevalence of skeletal muscle channelopathies. We determined the minimum point prevalence of genetically-defined skeletal muscle... 
Netherlands | Skeletal muscle channelopathies | Non-dystrophic myotonia | Prevalence | Periodic paralysis | ANDERSEN-TAWIL-SYNDROME | PHENOTYPE | NEUROSCIENCES | DUTCH | CLINICAL NEUROLOGY | CLCN1 MUTATIONS | MYOTONIA-CONGENITA | FAMILIES | HYPOKALEMIC PERIODIC PARALYSIS | Genetic research | Muscles | Genetic aspects | Paralysis | Gene mutations | Analysis
Journal Article
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, ISSN 1099-5129, 10/2018, Volume 20, Issue 10, pp. 1675 - 1682
Aims Andersen Tawil Syndrome (ATS) and catecholaminergic polymorphic ventricular tachycardia (CPVT) are both inherited arrhythmic disorders characterized by... 
Inherited arrhythmic disorders | Catecholaminergic polymorphic ventricular tachycardia | Andersen–Tawil syndrome | Tachyarrhythmias | Exercise | Diagnosis | ARRHYTHMIAS | CARDIAC & CARDIOVASCULAR SYSTEMS | LONG-QT SYNDROME | MODEL | KCNJ2 MUTATIONS | Andersen-Tawil syndrome | CALCIUM-RELEASE | SUDDEN CARDIAC DEATH | U-WAVE | Index Medicus
Journal Article
Journal of Shanghai Jiaotong University (Medical Science), ISSN 1674-8115, 01/2016, Volume 36, Issue 1, pp. 70 - 75
Journal Article
MATHEMATICAL BIOSCIENCES AND ENGINEERING, ISSN 1547-1063, 2019, Volume 16, Issue 4, pp. 2532 - 2548
In the last two decades, a group of proteins whose mutations are associated with a disease manifested by episodes of muscle weakness (periodic paralysis),... 
mutations | proteins | Andersen-Tawil syndrome | bioinformatics | channelopathies | KIR2.1 | MATHEMATICAL & COMPUTATIONAL BIOLOGY | high performance computing | Ion channels | structural bioinformatics | KCNJ2 MUTATIONS | PIM profile
Journal Article
No results were found for your search.

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