Literature DB >> 9326982

The phenotype/genotype relation and the current status of genetic screening in hypertrophic cardiomyopathy, Marfan syndrome, and the long QT syndrome.

J Burn1, J Camm, M J Davies, L Peltonen, P J Schwartz, H Watkins.   

Abstract

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Mesh：

Year:  1997        PMID： 9326982      PMCID： PMC484888          DOI： 10.1136/hrt.78.2.110

Source DB:  PubMed          Journal:  Heart        ISSN： 1355-6037            Impact factor:   5.994


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  35 in total

Review 1.  Marfan syndrome: genetic basis and clinical manifestations.

Authors:  P Tsipouras; R B Devereux
Journal:  Semin Dermatol       Date:  1993-09

2.  Fibrillin secretion and microfibril assembly by Marfan dermal fibroblasts.

Authors:  C M Kielty; J E Phillips; A H Child; F M Pope; C A Shuttleworth
Journal:  Matrix Biol       Date:  1994-03       Impact factor: 11.583

3.  A molecular approach to the stratification of cardiovascular risk in families with Marfan's syndrome.

Authors:  L Pereira; O Levran; F Ramirez; J R Lynch; B Sykes; R E Pyeritz; H C Dietz
Journal:  N Engl J Med       Date:  1994-07-21       Impact factor: 91.245

4.  Improved survival with amiodarone in patients with hypertrophic cardiomyopathy and ventricular tachycardia.

Authors:  W J McKenna; C M Oakley; D M Krikler; J F Goodwin
Journal:  Br Heart J       Date:  1985-04

5.  Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.

Authors:  L Thierfelder; H Watkins; C MacRae; R Lamas; W McKenna; H P Vosberg; J G Seidman; C E Seidman
Journal:  Cell       Date:  1994-06-03       Impact factor: 41.582

6.  Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families.

Authors:  J A Towbin; H Li; R T Taggart; M H Lehmann; P J Schwartz; C A Satler; R Ayyagari; J L Robinson; A Moss; J F Hejtmancik
Journal:  Circulation       Date:  1994-12       Impact factor: 29.690

Review 7.  Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy.

Authors:  H Watkins; J G Seidman; C E Seidman
Journal:  Hum Mol Genet       Date:  1995       Impact factor: 6.150

8.  Left cardiac sympathetic denervation in the therapy of congenital long QT syndrome. A worldwide report.

Authors:  P J Schwartz; E H Locati; A J Moss; R S Crampton; R Trazzi; U Ruberti
Journal:  Circulation       Date:  1991-08       Impact factor: 29.690

9.  Mutations in the fibrillin gene responsible for dominant ectopia lentis and neonatal Marfan syndrome.

Authors:  K Kainulainen; L Karttunen; L Puhakka; L Sakai; L Peltonen
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330

10.  Abnormal fibrillin assembly by dermal fibroblasts from two patients with Marfan syndrome.

Authors:  C M Kielty; C A Shuttleworth
Journal:  J Cell Biol       Date:  1994-03       Impact factor: 10.539
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  1 in total

Review 1.  Hypertrophic cardiomyopathy in childhood.

Authors:  Steven D Colan
Journal:  Heart Fail Clin       Date:  2010-10       Impact factor: 3.179
  1 in total

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