Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
2005 1
2008 1
2009 1
2021 1
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

5 results

Results by year

Filters applied: . Clear all
Page 1
Catecholaminergic polymorphic ventricular tachycardia.
Francis J, Sankar V, Nair VK, Priori SG. Francis J, et al. Heart Rhythm. 2005 May;2(5):550-4. doi: 10.1016/j.hrthm.2005.01.024. Heart Rhythm. 2005. PMID: 15840485 Review.
Catecholaminergic polymorphic ventricular tachycardia (VT) is a rare arrhythmogenic disease characterized by exercise- or stress-induced ventricular tachyarrhythmias, syncope, or sudden death, usually in the pediatric age group. ...Ankyrin-B mutations may also be im …
Catecholaminergic polymorphic ventricular tachycardia (VT) is a rare arrhythmogenic disease characterized by exercise- or stress-indu …
Catheter ablation of frequent monomorphic ventricular arrhythmias in Andersen-Tawil syndrome: case report and focused literature review.
Keegan R, Onetto L, Gregorietti F, Urruti R, Di Biase L. Keegan R, et al. J Interv Card Electrophysiol. 2023 Apr;66(3):729-736. doi: 10.1007/s10840-021-01077-w. Epub 2021 Oct 19. J Interv Card Electrophysiol. 2023. PMID: 34665385 Review.
BACKGROUND/PURPOSE: Andersen-Tawil syndrome type 1 is a rare autosomal dominant disease caused by a KCNJ2 gene mutation and clinically characterized by dysmorphic features, periodic muscular paralysis, and frequent ventricular arrhythmias (VAs). Although polymorphic and …
BACKGROUND/PURPOSE: Andersen-Tawil syndrome type 1 is a rare autosomal dominant disease caused by a KCNJ2 gene mutation and clinically chara …
Mechanisms and clinical management of inherited channelopathies: long QT syndrome, Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia, and short QT syndrome.
Kaufman ES. Kaufman ES. Heart Rhythm. 2009 Aug;6(8 Suppl):S51-5. doi: 10.1016/j.hrthm.2009.02.009. Epub 2009 Feb 12. Heart Rhythm. 2009. PMID: 19631908 Review.
In addition to avoidance QT-prolonging drugs and high intensity sports, standard treatment for LQTS involves anti-adrenergic therapy, with implantable cardioverter-defibrillator (ICD) use in high risk subgroups. Brugada Syndrome is associated with right ventricular conduct …
In addition to avoidance QT-prolonging drugs and high intensity sports, standard treatment for LQTS involves anti-adrenergic therapy, with i …
[A new type of periodic paralysis: Andersen-Tawil syndrome].
Pouget J. Pouget J. Bull Acad Natl Med. 2008 Nov;192(8):1551-6; discussion 1556-7. Bull Acad Natl Med. 2008. PMID: 19445372 Review. French.
Cardiac manifestations are variable and may include a long QT syndrome, premature ventricular contractions, complex ventricular ectopy, and polymorphic or bidirectional ventricular tachycardia. ...
Cardiac manifestations are variable and may include a long QT syndrome, premature ventricular contractions, complex ventric …
[Familial polymorph ventricular extrasystole associated with Pierre Robin syndrome].
Kieny JR, Stoll C, Roul G, Hessel F, Bareiss P, Sacrez A. Kieny JR, et al. Arch Mal Coeur Vaiss. 1992 Nov;85(11):1559-62. Arch Mal Coeur Vaiss. 1992. PMID: 1284460 Review. French.
In a family of 9 persons over 3 generations, 6 had incessant polymorphic ventricular extrasystoles, often in salves, resembling unsustained bidirectional ventricular tachycardia. Ventricular repolarisation was abnormal with giant U waves. Five persons …
In a family of 9 persons over 3 generations, 6 had incessant polymorphic ventricular extrasystoles, often in salves, resembling unsus …