(Q61897156)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

review article

1 reference

title

Hypertrophic cardiomyopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

author name string

Carolyn Y Ho

series ordinal

1

0 references

language of work or name

English

0 references

publication date

1 April 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

published in

Heart failure clinics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

page(s)

141-159

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

A molecular map of the interactions between titin and myosin-binding protein C. Implications for sarcomeric assembly in familial hypertrophic cardiomyopathy

29 January 2020

cites work

1 reference

12 December 2020

Sudden death due to troponin T mutations

1 reference

12 December 2020

Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Altered crossbridge kinetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy

1 reference

12 December 2020

The pathogenesis of familial hypertrophic cardiomyopathy: early and evolving effects from an alpha-cardiac myosin heavy chain missense mutation

1 reference

12 December 2020

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

1 reference

12 December 2020

Proposal for contemporary screening strategies in families with hypertrophic cardiomyopathy

1 reference

12 December 2020

Glycogen storage diseases presenting as hypertrophic cardiomyopathy.

1 reference

12 December 2020

The genetic basis for cardiac remodeling

1 reference

12 December 2020

Dilated-hypokinetic evolution of hypertrophic cardiomyopathy: prevalence, incidence, risk factors, and prognostic implications in pediatric and adult patients

1 reference

12 December 2020

Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia

1 reference

12 December 2020

Sarcomeric proteins and familial hypertrophic cardiomyopathy: linking mutations in structural proteins to complex cardiovascular phenotypes

1 reference

12 December 2020

Diltiazem treatment prevents diastolic heart failure in mice with familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Genotype-phenotype relationships involving hypertrophic cardiomyopathy-associated mutations in titin, muscle LIM protein, and telethonin

1 reference

12 December 2020

Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study

1 reference

12 December 2020

Arrhythmogenic right ventricular cardiomyopathy: moving toward mechanism

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypertrophic cardiomyopathy is predominantly a disease of left ventricular outflow tract obstruction

1 reference

12 December 2020

Agalsidase-beta therapy for advanced Fabry disease: a randomized trial

1 reference

12 December 2020

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Occurrence and Frequency of Arrhythmias in Hypertrophic Cardiomyopathy in Relation to Delayed Enhancement on Cardiovascular Magnetic Resonance

1 reference

12 December 2020

Shared genetic causes of cardiac hypertrophy in children and adults

1 reference

12 December 2020

Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy

1 reference

12 December 2020

The use of contrast-enhanced magnetic resonance imaging to identify reversible myocardial dysfunction

1 reference

12 December 2020

An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Sudden death in hypertrophic cardiomyopathy: identification of high risk patients.

1 reference

12 December 2020

Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy

1 reference

12 December 2020

R403Q and L908V mutant beta-cardiac myosin from patients with familial hypertrophic cardiomyopathy exhibit enhanced mechanical performance at the single molecule level

1 reference

12 December 2020

Relation between severity of left-ventricular hypertrophy and prognosis in patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

1 reference

12 December 2020

Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (I79N) mutation linked to familial hypertrophic cardiomyopathy

1 reference

12 December 2020

The molecular genetic basis for hypertrophic cardiomyopathy

1 reference

12 December 2020

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

1 reference

12 December 2020

Identification of a gene responsible for familial Wolff-Parkinson-White syndrome

1 reference

12 December 2020

Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy

1 reference

12 December 2020

Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy

1 reference

12 December 2020

Relation between myocyte disarray and outcome in hypertrophic cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy: management, risk stratification, and prevention of sudden death

1 reference

12 December 2020

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

1 reference

12 December 2020

Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy: a systematic review

1 reference

12 December 2020

Prevalence of Anderson-Fabry disease in male patients with late onset hypertrophic cardiomyopathy

1 reference

12 December 2020

The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model

1 reference

12 December 2020

Assessment of Diastolic Function With Doppler Tissue Imaging to Predict Genotype in Preclinical Hypertrophic Cardiomyopathy

1 reference

12 December 2020

Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers.

1 reference

12 December 2020

Genetic testing and genetic counselling in hypertrophic cardiomyopathy: the French experience

1 reference

12 December 2020

Myocardial scarring in asymptomatic or mildly symptomatic patients with hypertrophic cardiomyopathy

1 reference

12 December 2020

Effect of Left Ventricular Outflow Tract Obstruction on Clinical Outcome in Hypertrophic Cardiomyopathy

1 reference

12 December 2020

Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

A Missense Mutation in the CASQ2 Gene Is Associated with Autosomal-Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia

1 reference

12 December 2020

Toward clinical risk assessment in hypertrophic cardiomyopathy with gadolinium cardiovascular magnetic resonance.

1 reference

12 December 2020

Gadolinium-enhanced magnetic resonance imaging in hypertrophic cardiomyopathy: in vivo imaging of the pathologic substrate for premature cardiac death?

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

1 reference

12 December 2020

Clinical course of hypertrophic cardiomyopathy with survival to advanced age.

1 reference

12 December 2020

Sudden death in young athletes

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevalence of idiopathic hypertrophic cardiomyopathy in China: a population-based echocardiographic analysis of 8080 adults

1 reference

12 December 2020

Aldosterone, through novel signaling proteins, is a fundamental molecular bridge between the genetic defect and the cardiac phenotype of hypertrophic cardiomyopathy

1 reference

12 December 2020

Clinical practice. Hypertrophic obstructive cardiomyopathy

1 reference

12 December 2020

Hypertrophic cardiomyopathy

1 reference

12 December 2020

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia

1 reference

12 December 2020

Hypertrophy, fibrosis, and sudden cardiac death in response to pathological stimuli in mice with mutations in cardiac troponin T.

1 reference

12 December 2020

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

1 reference

12 December 2020

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

1 reference

12 December 2020

Structure of the actin-myosin complex and its implications for muscle contraction

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

An Atypical Variant of Fabry's Disease in Men with Left Ventricular Hypertrophy

1 reference

12 December 2020

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

1 reference

12 December 2020

Phenotypic spectrum and patterns of left ventricular hypertrophy in hypertrophic cardiomyopathy: Morphologic observations and significance as assessed by two-dimensional echocardiography in 600 patients

1 reference

12 December 2020

A mouse model of familial hypertrophic cardiomyopathy

1 reference

12 December 2020

The Genetic Basis for Cardiomyopathy

1 reference

12 December 2020

10.1016/J.HFC.2009.12.001

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20347784%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

PubMed publication ID

20347784

1 reference