Inherited ion channel diseases: a brief review - Wikidata - awgldk - TriplyDB

Inherited ion channel diseases: a brief review

Inherited ion channel diseases: a brief review

http://www.wikidata.org/entity/Q28071914

about

Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association Pre-participation cardiovascular evaluation for athletic participants to prevent sudden death: Position paper from the EHRA and the EACPR, branches of the ESC. Endorsed by APHRS, HRS, and SOLAECE.Potassium currents in the heart: functional roles in repolarization, arrhythmia and therapeutics.Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications.A clinical approach to arrhythmias revisited in 2018 : From ECG over noninvasive and invasive electrophysiology to advanced imaging.Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death.Sinus Bradycardia in Carriers of the SCN5A-1795insD Mutation: Unraveling the Mechanism through Computer Simulations.Calcium in Brugada Syndrome: Questions for Future Research SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta-analysis Magnetocardiography on an isolated animal heart with a room-temperature optically pumped magnetometer Pre-participation cardiovascular evaluation for athletic participants to prevent sudden death: Position paper from the EHRA and the EACPR, branches of the ESC. Endorsed by APHRS, HRS, and SOLAECE

P2860

Q30238784-546918EB-309A-4EA4-A5F4-CC56C02EEB00 Q40488679-DD0B73F3-9BF2-4F8E-9ECE-DE9AD2FA5345 Q43920140-5470B370-99AA-4A49-896B-FCA156CFD38A Q45875036-D91CEE82-95CF-4FE4-A23D-8DAC91F1F3F0 Q49024258-D53CA50C-F580-492B-8C8F-DB9741065C78 Q49574372-76515885-8FE7-46B4-9AB5-703F1676D2B9 Q51748513-A5DDCCD9-28F5-41C1-91BC-EA1759D78591 Q57169914-5395318C-A846-440E-8976-A7BF256B206D Q57495982-212EAAFD-90AD-4B3E-AF5D-779AF80CD7E3 Q58577802-CD387DF3-27E4-4081-B5A3-5292DFF04E2C Q58757143-0D376E49-28FD-4E6B-B36D-5ED976F89EDF

P2860

Inherited ion channel diseases: a brief review

http://www.wikidata.org/entity/Q28071914

description

2015 nî lūn-bûn

@nan

2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Inherited ion channel diseases: a brief review

@ast

Inherited ion channel diseases: a brief review

@en

Inherited ion channel diseases: a brief review

@nl

type

label

Inherited ion channel diseases: a brief review

@ast

Inherited ion channel diseases: a brief review

@en

Inherited ion channel diseases: a brief review

@nl

prefLabel

Inherited ion channel diseases: a brief review

@ast

Inherited ion channel diseases: a brief review

@en

Inherited ion channel diseases: a brief review

@nl

P1433

Q28071914-762E575F-0BA4-43AB-B7B2-A6F3832F39D4

P1476

Q28071914-2025B768-635E-4FF4-84CE-61679F8FF58E

P2093

Q28071914-896C685D-2D27-4415-8BC0-7C27E1CD1C26

Q28071914-F3F1B5C5-E14A-40DD-A506-EBF60ED3E254

P2860

Q28071914-038EC76C-BC0D-4F82-AF79-994129C3C286

Q28071914-07A137D6-BC03-4D9E-BC59-4DBA9D965909

Q28071914-117D1B10-5D9B-49E6-8939-A60481C3463A

Q28071914-2E6DEC07-84EB-4891-B393-E6B691C252DD

Q28071914-366557D4-3AD0-4D76-86BC-BD27B1E7E941

Q28071914-39F8FAA8-17F0-4745-AC2E-4C87251DD70B

Q28071914-3B262D71-529F-4E70-89CF-0EAB6B7FEC43

Q28071914-48AF77A0-8473-4EED-B911-7F70BCB0D721

Q28071914-4A27B831-9F0A-48FF-92D6-A09D713873AE

Q28071914-529B6C8F-AE53-4690-9AF1-CCB7C9835F01

P304

Q28071914-9F6C4094-B0CF-4791-9A99-1D5691BFE509

P31

Q28071914-19832B45-9AC0-4B24-B497-37C5D07A2CE2

P356

Q28071914-B092A9A5-967F-4FCC-8669-AEC922AD44F2

P407

Q28071914-93F12487-0A81-4313-8160-A082E73FDFBB

P478

Q28071914-E48D3B6A-0208-47A1-BDA7-9195914BFEDE

P577

Q28071914-C4FEC771-DC95-42F3-9CAA-2712A69EA9F9

P698

Q28071914-6C501E0C-2DDE-4C63-914E-A1DCA0B471C3

P356

P1433

P1476

Inherited ion channel diseases: a brief review

@en

P2093

Arthur A.M. Wilde

http://www.w3.org/2001/XMLSchema#string

Krystien V.V. Lieve

http://www.w3.org/2001/XMLSchema#string

P2860

A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene

Mutations in calmodulin cause ventricular tachycardia and sudden cardiac death

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

Drugs and Brugada syndrome patients: review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

Genetic basis and molecular mechanism for idiopathic ventricular fibrillation

Left cardiac sympathetic denervation for catecholaminergic polymorphic ventricular tachycardia

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

P304

ii1-6

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1093/EUROPACE/EUV105

http://www.w3.org/2001/XMLSchema#string

P407

P478

17 Suppl 2

http://www.w3.org/2001/XMLSchema#string

P577

2015-10-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26842110

http://www.w3.org/2001/XMLSchema#string