Research priorities in hypertrophic cardiomyopathy: report of a Working Group of the National Heart, Lung, and Blood Institute. (Q34759446)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20837938%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Research priorities in hypertrophic cardiomyopathy: report of a Working Group of the National Heart, Lung, and Blood Institute (English)

1 reference

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hypertrophic cardiomyopathy

13 February 2020

main subject

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1 reference

1

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Ray E Hershberger

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Raghu Kalluri

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Jeffery D. Molkentin

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Rong Tian

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Steven R Houser

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Christine E Seidman

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Barry J Maron

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13 February 2020

author name string

Robert O Bonow

2

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13 February 2020

R John Solaro

4

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13 February 2020

Bishow Adhikari

6

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13 February 2020

Mark E Anderson

7

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13 February 2020

Robin Boineau

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13 February 2020

Barry J Byrne

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Thomas P Cappola

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13 February 2020

Martin M LeWinter

12

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13 February 2020

Martin S Maron

13

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13 February 2020

Steve R Ommen

15

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13 February 2020

Michael Regnier

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13 February 2020

W H Wilson Tang

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13 February 2020

Marvin A Konstam

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13 February 2020

language of work or name

English

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publication date

1 September 2010

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13 February 2020

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13 February 2020

volume

122

1 reference

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13 February 2020

issue

11

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page(s)

1130-1133

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How should hypertrophic cardiomyopathy be classified?: What's in a name? Dilemmas in nomenclature characterizing hypertrophic cardiomyopathy and left ventricular hypertrophy

13 February 2020

cites work

1 reference

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Progress with genetic cardiomyopathies: screening, counseling, and testing in dilated, hypertrophic, and arrhythmogenic right ventricular dysplasia/cardiomyopathy.

7 July 2018

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Evidence from human myectomy samples that MYBPC3 mutations cause hypertrophic cardiomyopathy through haploinsufficiency

7 July 2018

1 reference

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Clinical outcome and phenotypic expression in LAMP2 cardiomyopathy

7 July 2018

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The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders

7 July 2018

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Shared genetic causes of cardiac hypertrophy in children and adults

7 July 2018

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Genetic determinants of cardiac hypertrophy

7 July 2018

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Hypertrophic cardiomyopathy: the genetic determinants of clinical disease expression

7 July 2018

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Management of symptoms in hypertrophic cardiomyopathy

7 July 2018

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Risk stratification of sudden cardiac death in hypertrophic cardiomyopathy

7 July 2018

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Genetics of hypertrophic cardiomyopathy: one, two, or more diseases?

7 July 2018

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Reviews of translational medicine and genomics in cardiovascular disease: new disease taxonomy and therapeutic implications cardiomyopathies: therapeutics based on molecular phenotype

7 July 2018

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Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

7 July 2018

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ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

7 July 2018

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Clinical genetics in cardiology

7 July 2018

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A contemporary approach to hypertrophic cardiomyopathy.

7 July 2018

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7 July 2018

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Gene mutations in apical hypertrophic cardiomyopathy

7 July 2018

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Historical trends in reported survival rates in patients with hypertrophic cardiomyopathy

7 July 2018

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7 July 2018

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Genetic testing for risk stratification in hypertrophic cardiomyopathy and long QT syndrome: fact or fiction?

7 July 2018

1 reference

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Familial hypertrophic cardiomyopathy: clinical features, molecular genetics and molecular genetic testing

7 July 2018

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American College of Cardiology/European Society of Cardiology clinical expert consensus document on hypertrophic cardiomyopathy. A report of the American College of Cardiology Foundation Task Force on Clinical Expert Consensus Documents and the Euro

7 July 2018

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Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy

7 July 2018

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Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

7 July 2018

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Hypertrophic cardiomyopathy: a systematic review

7 July 2018

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Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene

7 July 2018

1 reference

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Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy

7 July 2018

1 reference

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Sudden death due to troponin T mutations

7 July 2018

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Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

7 July 2018

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Prevalence of hypertrophic cardiomyopathy in a general population of young adults. Echocardiographic analysis of 4111 subjects in the CARDIA Study. Coronary Artery Risk Development in (Young) Adults

7 July 2018

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Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

7 July 2018

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The case for myocardial ischemia in hypertrophic cardiomyopathy

7 July 2018

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Prevalence, clinical significance, and natural history of left ventricular apical aneurysms in hypertrophic cardiomyopathy

26 October 2018

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Myofilament protein gene mutation screening and outcome of patients with hypertrophic cardiomyopathy

26 October 2018

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ACC/AHA/ESC 2006 guidelines for management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association Task Force and the European Society of Cardiolo

26 October 2018

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Prevalence, clinical profile, and significance of left ventricular remodeling in the end-stage phase of hypertrophic cardiomyopathy

26 October 2018

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Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

26 October 2018

1 reference

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Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

26 October 2018

1 reference

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Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3070356

Clinical course of hypertrophic cardiomyopathy with survival to advanced age.

26 October 2018

1 reference

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Hypertrophic cardiomyopathy due to sarcomeric gene mutations is characterized by impaired energy metabolism irrespective of the degree of hypertrophy

26 October 2018

1 reference

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The Incidence of Pediatric Cardiomyopathy in Two Regions of the United States

26 October 2018

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The Epidemiology of Childhood Cardiomyopathy in Australia

26 October 2018

1 reference

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Relationship of race to sudden cardiac death in competitive athletes with hypertrophic cardiomyopathy.

26 October 2018

1 reference

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Spectrum of clinical phenotypes and gene variants in cardiac myosin-binding protein C mutation carriers with hypertrophic cardiomyopathy.

26 October 2018

1 reference

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Clinical course of hypertrophic cardiomyopathy in a regional United States cohort

26 October 2018

1 reference

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Epidemiology of Hypertrophic Cardiomyopathy–Related Death

26 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20837938

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Impact of Atrial Fibrillation on the Clinical Course of Hypertrophic Cardiomyopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20837938

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genotype–phenotype correlations in familial hypertrophic cardiomyopathy A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20837938

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1161/CIRCULATIONAHA.110.950089

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20837938%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20837938%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

PubMed publication ID

20837938

1 reference