Literature DB >> 8080508

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.

R Tawil1, L J Ptacek, S G Pavlakis, D C DeVivo, A S Penn, C Ozdemir, R C Griggs.   

Abstract

Andersen's syndrome is a clinically distinct form of potassium-sensitive periodic paralysis associated with cardiac dysrhythmias. The subtle nature of the cardiac and dysmorphic features may delay the recognition of this syndrome and its potentially lethal cardiac dysrhythmias. The genetic defect in Andersen's syndrome is not genetically linked to other forms of potassium-sensitive periodic paralysis and is probably distinct from the long QT syndrome locus.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 8080508     DOI: 10.1002/ana.410350313

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  67 in total

Review 1.  Periodic paralysis: understanding channelopathies.

Authors:  Frank Lehmann-Horn; Karin Jurkat-Rott; Reinhardt Rüdel
Journal:  Curr Neurol Neurosci Rep       Date:  2002-01       Impact factor: 5.081

2.  Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome.

Authors:  Regina Preisig-Müller; Günter Schlichthörl; Tobias Goerge; Steffen Heinen; Andrea Brüggemann; Sindhu Rajan; Christian Derst; Rüdiger W Veh; Jürgen Daut
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-28       Impact factor: 11.205

Review 3.  Muscle channelopathies and critical points in functional and genetic studies.

Authors:  Karin Jurkat-Rott; Frank Lehmann-Horn
Journal:  J Clin Invest       Date:  2005-08       Impact factor: 14.808

Review 4.  Diagnostics and therapy of muscle channelopathies--Guidelines of the Ulm Muscle Centre.

Authors:  F Lehmann-Horn; K Jurkat-Rott; R Rüdel
Journal:  Acta Myol       Date:  2008-12

Review 5.  Genotype- and phenotype-guided management of congenital long QT syndrome.

Authors:  John R Giudicessi; Michael J Ackerman
Journal:  Curr Probl Cardiol       Date:  2013-10       Impact factor: 5.200

6.  The Twiddling Andersen.

Authors:  John L Jefferies; Jeffrey J Kim; John W Belmont; Richard A Friedman
Journal:  Tex Heart Inst J       Date:  2009

7.  Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Authors:  Martin Tristani-Firouzi; Judy L Jensen; Matthew R Donaldson; Valeria Sansone; Giovanni Meola; Angelika Hahn; Said Bendahhou; Hubert Kwiecinski; Anna Fidzianska; Nikki Plaster; Ying-Hui Fu; Louis J Ptacek; Rabi Tawil
Journal:  J Clin Invest       Date:  2002-08       Impact factor: 14.808

8.  Novel mutation in the KCNJ2 gene is associated with a malignant arrhythmic phenotype of Andersen-Tawil syndrome.

Authors:  E Fernlund; C Lundin; E Hertervig; O Kongstad; M Alders; P Platonov
Journal:  Ann Noninvasive Electrocardiol       Date:  2013-09       Impact factor: 1.468

9.  An algorithm for candidate sequencing in non-dystrophic skeletal muscle channelopathies.

Authors:  Tai-Seung Nam; Christoph Lossin; Dong-Uk Kim; Myeong-Kyu Kim; Young-Ok Kim; Kang-Ho Choi; Seok-Yong Choi; Sang-Cheol Park; In-Seop Na
Journal:  J Neurol       Date:  2013-03-03       Impact factor: 4.849

10.  Resuscitated sudden cardiac death in Andersen-Tawil syndrome.

Authors:  Kelly J Airey; Susan P Etheridge; Rabi Tawil; Martin Tristani-Firouzi
Journal:  Heart Rhythm       Date:  2009-08-29       Impact factor: 6.343

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.