Idiopathic hypertrophic cardiomyopathy in identical twins. Morphological heterogeneity of the left ventricle.

No abstract is available for this paper.

• Publication year

  1992

• Venue

  Chest

• Publication date

  1992-09-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1378/CHEST.102.3.783PMID 1516403
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene.

  1990cited by this paper
• A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.

  1990cited by this paper
• Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.

  1990cited by this paper
• A molecular basis for familial hypertrophic cardiomyopathy: An αβ cardiac myosin heavy chain hybrid gene

  1990cited by this paper
• Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

  1989cited by this paper
• Hypertrophic cardiomyopathy in identical twins.

  1989cited by this paper
• Inheritance of hypertrophic cardiomyopathy: a cross sectional and M mode echocardiographic study of 50 families.

  1987cited by this paper
• The genetics of hypertrophic cardiomyopathy.

  1986cited by this paper
• Patterns of inheritance in hypertrophic cardiomyopathy: assessment by M-mode and two-dimensional echocardiography.

  1984cited by this paper
• Heterogeneous Morphologic Expression of Genetically Transmitted Hypertrophic Cardiomyopathy: Two–dimensional Echocardiographic Analysis

  1983cited by this paper
• Familial prevalence and genetic transmission of idiopathic hypertrophic subaortic stenosis.

  1973cited by this paper
• Twin studies in hypertrophic cardiomyopathy.

  1972cited by this paper

• Twin Phenomena of Hypertrophic Cardiomyopathy: A Reported Case Series

  2024cites this paper
• Hypertrophic cardiomyopathy in identical twins: a case series

  2022cites this paper
• Heritability and Pedigree Analyses of Hypertrophic Cardiomyopathy in Rhesus Macaques (Macaca Mulatta)

  2021cites this paper
• Adult Monozygotic Twins With Hypertrophic Cardiomyopathy and Identical Disease Expression and Clinical Course.

  2020cites this paper
• Different Clinical Presentation and Tissue Characterization in a Monozygotic Twin Pair with MYH7 Mutation-Related Hypertrophic Cardiomyopathy.

  2019cites this paper
• Heritability in genetic heart disease: the role of genetic background

  2019cites this paper
• Determined to Fail—the Role of Genetic Mechanisms in Heart Failure

  2015cites this paper
• Monoamniotic monochorionic twins discordant for noncompaction cardiomyopathy

  2013cites this paper
• Molecular genetics in hypertrophic cardiomyopathy: towards individualized management of the disease

  2006cites this paper
• The pathology of hypertrophic cardiomyopathy

  2004cites this paper
• Hypertrophic Cardiomyopathy with Shared Morphology in Identical Twins: A Case Report

  2002cites this paper
• A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy.

  2001cites this paper
• Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7A797T mutation

  2000cites this paper
• Use of MRI and audiological tests in presymptomatic diagnosis of type 2 neurofibromatosis (NF2)

  2000cites this paper
• Germline and somatic mosaicism in achondroplasia.

  2000cites this paper
• Genotype‐phenotype analysis in four families with mutations in β‐myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy

  1998cites this paper
• [Clinical application of the genetic aspects of familial hypertrophic cardiomyopathy].

  1998cites this paper
• Dilated Cardiomyopathy in Transgenic Mice With Cardiac-Specific Overexpression of Tumor Necrosis Factor-α

  1997cites this paper
• Dilated cardiomyopathy in transgenic mice with cardiac-specific overexpression of tumor necrosis factor-alpha.

  1997cites this paper
• Mapping the locus for familial hypertrophic cardiomyopathy to chromosome 11 in a family with a case of apical hypertrophic cardiomyopathy of the Japanese type

  1996cites this paper
• [Genetics of hypertrophic cardiomyopathies: what are the clinical perspectives?].

  1996cites this paper
• Contractile protein mutations and heart disease.

  1996cites this paper
• Molecular Pathology of Dilated Cardiomyopathies.

  1996cites this paper
• Mice Expressing Mutant Myosin Heavy Chains Are a Model for Familial Hypertrophic Cardiomyopathy

  1996cites this paper
• Molecular basis of familial cardiomyopathies.

  1995cites this paper
• [Demonstration of a fifth locus implicated in familial hypertrophic cardiomyopathies].

  1994cites this paper