Literature DB >> 4106724

Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

E D Andersen, P A Krasilnikoff, H Overvad.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1971        PMID: 4106724     DOI: 10.1111/j.1651-2227.1971.tb06990.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


× No keyword cloud information.
  48 in total

Review 1.  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

2.  The Twiddling Andersen.

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

3.  Asymptomatic cardiac arrhythmias in periodic paralysis.

Authors:  U Bonuccelli; A Nuti; L Paperini; M G Bongiorni; A Arrigo; C Contini; A Muratorio
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-01       Impact factor: 10.154

4.  Golgi export of the Kir2.1 channel is driven by a trafficking signal located within its tertiary structure.

Authors:  Donghui Ma; Tarvinder Kaur Taneja; Brian M Hagen; Bo-Young Kim; Bernardo Ortega; W Jonathan Lederer; Paul A Welling
Journal:  Cell       Date:  2011-06-24       Impact factor: 41.582

5.  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

6.  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

Review 7.  Andersen syndrome: the newest variant of the hereditary-familial long QT syndrome.

Authors:  Andrés Ricardo Pérez Riera; Celso Ferreira; Sérgio J Dubner; Edgardo Schapachnik
Journal:  Ann Noninvasive Electrocardiol       Date:  2004-04       Impact factor: 1.468

8.  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

9.  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

10.  KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes.

Authors:  Gregor Andelfinger; Andrew R Tapper; Richard C Welch; Carlos G Vanoye; Alfred L George; D Woodrow Benson
Journal:  Am J Hum Genet       Date:  2002-07-29       Impact factor: 11.025

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.