Literature DB >> 9093029

Dilated cardiomyopathy: a genetic approach.

L Mestroni.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9093029      PMCID: PMC484677          DOI: 10.1136/hrt.77.3.185

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


× No keyword cloud information.
  17 in total

1.  Dilated cardiomyopathy associated with deficiency of the cytoskeletal protein metavinculin.

Authors:  M Maeda; E Holder; B Lowes; S Valent; R D Bies
Journal:  Circulation       Date:  1997-01-07       Impact factor: 29.690

Review 2.  Genetic factors in dilated cardiomyopathy.

Authors:  L Mestroni; J Milasin; M Vatta; B Pinamonti; G Sinagra; C Rocco; M Matulic; A Falaschi; M Giacca; F Camerini
Journal:  Arch Mal Coeur Vaiss       Date:  1996-07

3.  Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

Authors:  K R Bowles; R Gajarski; P Porter; V Goytia; L Bachinski; R Roberts; R Pignatelli; J A Towbin
Journal:  J Clin Invest       Date:  1996-09-15       Impact factor: 14.808

4.  Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

Authors:  J B Durand; L L Bachinski; L C Bieling; G Z Czernuszewicz; A B Abchee; Q T Yu; T Tapscott; R Hill; J Ifegwu; A J Marian
Journal:  Circulation       Date:  1995-12-15       Impact factor: 29.690

5.  Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group.

Authors:  M Krajinovic; B Pinamonti; G Sinagra; M Vatta; G M Severini; J Milasin; A Falaschi; F Camerini; M Giacca; L Mestroni
Journal:  Am J Hum Genet       Date:  1995-10       Impact factor: 11.025

6.  Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984.

Authors:  M B Codd; D D Sugrue; B J Gersh; L J Melton
Journal:  Circulation       Date:  1989-09       Impact factor: 29.690

7.  Mapping a cardiomyopathy locus to chromosome 3p22-p25.

Authors:  T M Olson; M T Keating
Journal:  J Clin Invest       Date:  1996-01-15       Impact factor: 14.808

8.  A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1.

Authors:  S Kass; C MacRae; H L Graber; E A Sparks; D McNamara; H Boudoulas; C T Basson; P B Baker; R J Cody; M C Fishman
Journal:  Nat Genet       Date:  1994-08       Impact factor: 38.330

9.  Familial dilated cardiomyopathy in the United Kingdom.

Authors:  P J Keeling; Y Gang; G Smith; H Seo; S E Bent; V Murday; A L Caforio; W J McKenna
Journal:  Br Heart J       Date:  1995-05

10.  A point mutation in the 5' splice site of the dystrophin gene first intron responsible for X-linked dilated cardiomyopathy.

Authors:  J Milasin; F Muntoni; G M Severini; L Bartoloni; M Vatta; M Krajinovic; A Mateddu; C Angelini; F Camerini; A Falaschi; L Mestroni; M Giacca
Journal:  Hum Mol Genet       Date:  1996-01       Impact factor: 6.150

View more
  1 in total

1.  Lack of effects of recombinant human growth hormone in a child with a complex cardiovascular malformation and dilated cardiomyopathy.

Authors:  L Rosti; E Cerini; P Festa; A Miola; V Brunelli; A Frigiola
Journal:  J Endocrinol Invest       Date:  2000-01       Impact factor: 4.256

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.