Literature DB >> 570800

Prevalence of dignostic abnormalities in patients with genetically transmitted asymmetric septal hypertrophy.

F J ten Cate, P G Hugenholtz, W G van Dorp, J Roelandt.   

Abstract

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Year:  1979        PMID： 570800     DOI： 10.1016/0002-9149(79)90071-7

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN： 0002-9149            Impact factor:   2.778


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  10 in total

Review 1.  Clues in diagnosing congenital heart disease.

Authors:  A J Moss
Journal:  West J Med       Date:  1992-04

2.  Asymmetric septal hypertrophy and hypertrophic cardiomyopathy.

Authors:  R Emanuel; J Marcomichelakis; R Withers; K O'Brien
Journal:  Br Heart J       Date:  1983-04

3.  Left ventricular wall thickness and regional systolic function in patients with hypertrophic cardiomyopathy. A three-dimensional tagged magnetic resonance imaging study.

Authors:  S J Dong; J H MacGregor; A P Crawley; E McVeigh; I Belenkie; E R Smith; J V Tyberg; R Beyar
Journal:  Circulation       Date:  1994-09       Impact factor: 29.690

4.  Familial spontaneous complete heart block in hypertrophic cardiomyopathy.

Authors:  E K Louie; B J Maron
Journal:  Br Heart J       Date:  1986-05

5.  Familial hypertrophic cardiomyopathy: vectorcardiographic findings in echocardiographically unaffected relative.

Authors:  F Loperfido; R Fiorilli; A Digaetano; M Di Gennaro; P Santarelli; F Bellocci; E Coppola; P Zecchi
Journal:  Br Heart J       Date:  1982-06

6.  The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study.

Authors:  Paula L Hedley; Ole Haundrup; Paal S Andersen; Frederik H Aidt; Morten Jensen; Johanna C Moolman-Smook; Henning Bundgaard; Michael Christiansen
Journal:  J Negat Results Biomed       Date:  2011-10-03

7.  Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

Authors:  Christian M Hagen; Frederik H Aidt; Ole Havndrup; Paula L Hedley; Morten K Jensen; Jørgen K Kanters; Tam T Pham; Henning Bundgaard; Michael Christiansen
Journal:  PLoS One       Date:  2015-04-29       Impact factor: 3.240

8.  A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity.

Authors:  Paal Skytt Andersen; Paula Louise Hedley; Stephen P Page; Petros Syrris; Johanna Catharina Moolman-Smook; William John McKenna; Perry Mark Elliott; Michael Christiansen
Journal:  Biochem Res Int       Date:  2012-04-11

9.  Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population.

Authors:  Christian M Hagen; Frederik H Aidt; Paula L Hedley; Morten K Jensen; Ole Havndrup; Jørgen K Kanters; Johanna C Moolman-Smook; Severin O Larsen; Henning Bundgaard; Michael Christiansen
Journal:  PLoS One       Date:  2013-08-05       Impact factor: 3.240

10.  MT-CYB mutations in hypertrophic cardiomyopathy.

Authors:  Christian M Hagen; Frederik H Aidt; Ole Havndrup; Paula L Hedley; Cathrine Jespersgaard; Morten Jensen; Jørgen K Kanters; Johanna C Moolman-Smook; Daniel V Møller; Henning Bundgaard; Michael Christiansen
Journal:  Mol Genet Genomic Med       Date:  2013-04-12       Impact factor: 2.183
  10 in total

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