Literature DB >> 6682724

Heterogeneous morphologic expression of genetically transmitted hypertrophic cardiomyopathy. Two-dimensional echocardiographic analysis.

E Ciró, P F Nichols, B J Maron.   

Abstract

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Year:  1983        PMID: 6682724     DOI: 10.1161/01.cir.67.6.1227

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


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  12 in total

1.  No evidence for linkage of familial hypertrophic cardiomyopathy and chromosome 14q1 locus D14S26 in a Chinese family: evidence for genetic heterogeneity.

Authors:  Y L Ko; W P Lien; J J Chen; C W Wu; T K Tang; C C Liew
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

Review 2.  Progress in familial hypertrophic cardiomyopathy: molecular genetic analyses in the original family studied by Teare.

Authors:  H Watkins; C E Seidman; C MacRae; J G Seidman; W McKenna
Journal:  Br Heart J       Date:  1992-01

3.  The genetics of hypertrophic cardiomyopathy.

Authors:  D M Gilligan; J G Cleland; C M Oakley
Journal:  Br Heart J       Date:  1991-09

4.  Hypertrophic cardiomyopathy in identical twins.

Authors:  J M Reid; A B Houston; E Lundmark
Journal:  Br Heart J       Date:  1989-11

Review 5.  Multiple disease genes cause hypertrophic cardiomyopathy.

Authors:  H Watkins
Journal:  Br Heart J       Date:  1994-12

6.  Whole-body distribution of iodine 123 metaiodobenzylguanidine in hypertrophic cardiomyopathy: significance of its washout from the heart.

Authors:  J Taki; K Nakajima; H Bunko; M Simizu; A Muramori; K Hisada
Journal:  Eur J Nucl Med       Date:  1990

7.  Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.

Authors:  Andreas Perrot; Hajo Schmidt-Traub; Bernard Hoffmann; Matthias Prager; Nana Bit-Avragim; Raisa I Rudenko; Dinara A Usupbaeva; Zhyldyz Kabaeva; Bakytbek Imanov; Mirsaid M Mirrakhimov; Rainer Dietz; Anna Wycisk; Michal Tendera; Reinhard Gessner; Karl Josef Osterziel
Journal:  J Mol Med (Berl)       Date:  2005-04-22       Impact factor: 4.599

8.  Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type.

Authors:  Y L Ko; J J Chen; T K Tang; M S Teng; S Y Lin; P Kuan; C W Wu; W P Lien; C C Liew
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

9.  Myocardial thallium defects in apical hypertrophic cardiomyopathy are associated with a benign prognosis. Thallium defects in apical hypertrophy.

Authors:  Kyung-Han Lee; Hong-Joo Jang; Sang Chul Lee; Young-Hwan Kim; Eun-Jung Lee; Jung-Don Seo; Byung-Tae Kim
Journal:  Int J Cardiovasc Imaging       Date:  2003-10       Impact factor: 2.357

10.  Familial spontaneous complete heart block in hypertrophic cardiomyopathy.

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