Literature DB >> 5093256

Familial sinus node disease.

R D Spellberg.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5093256     DOI： 10.1378/chest.60.3.246

Source DB:  PubMed          Journal:  Chest        ISSN： 0012-3692            Impact factor:   9.410


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  12 in total

1.  Rundown of the hyperpolarization-activated KAT1 channel involves slowing of the opening transitions regulated by phosphorylation.

Authors:  X D Tang; T Hoshi
Journal:  Biophys J       Date:  1999-06       Impact factor: 4.033

2.  Congenital sinus bradycardia combined with congenital total atrioventricular block.

Authors:  H Stopfkuchen; B K Jüngst
Journal:  Eur J Pediatr       Date:  1977-07-01       Impact factor: 3.183

3.  Familial idiopathic atrial fibrillation with bradyarrhythmia.

Authors:  H Bertram; T Paul; F Beyer; H C Kallfelz
Journal:  Eur J Pediatr       Date:  1996-01       Impact factor: 3.183

4.  Sinuatrial disease in young people.

Authors:  A F Mackintosh
Journal:  Br Heart J       Date:  1981-01

5.  Familial symptomatic sinus bradycardia: autosomal dominant inheritance.

Authors:  A V Mehta; B Chidambaram; A Garrett
Journal:  Pediatr Cardiol       Date:  1995 Sep-Oct       Impact factor: 1.655

6.  Familial sinus node disease and degenerative myopia--a new hereditary syndrome?

Authors:  A Onat
Journal:  Hum Genet       Date:  1986-02       Impact factor: 4.132

7.  Pacemaker channel dysfunction in a patient with sinus node disease.

Authors:  Eric Schulze-Bahr; Axel Neu; Patrick Friederich; U Benjamin Kaupp; Günter Breithardt; Olaf Pongs; Dirk Isbrandt
Journal:  J Clin Invest       Date:  2003-05       Impact factor: 14.808

8.  Familial automaticity-conduction disorder with associated cardiomyopathy.

Authors:  P R Greenlee; J L Anderson; J R Lutz; A E Lindsay; A D Hagan
Journal:  West J Med       Date:  1986-01

9.  Stroke complicating congenital sick sinus syndrome.

Authors:  R Lehmann; G Groenefeld; C W Israel
Journal:  Herzschrittmacherther Elektrophysiol       Date:  2007-06

10.  Familial sinus node dysfunction with autosomal dominant inheritance.

Authors:  H Lehmann; U E Klein
Journal:  Br Heart J       Date:  1978-11
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