Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.

Hypertrophic cardiomyopathy:a paradigm for myocardial energy depletion.

Genetic analysis of hypertrophic cardiomyopathy (HCM), a mendelian form of cardiac hypertrophy, indicates that the primary defect is in sarcomeric function. However, the initial proposal that depressed myocardial contraction leads to a 'compensatory' hypertrophy has proven inconsistent wit...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Ashrafian, H, Redwood, C, Blair, E, Watkins, H
التنسيق:	Journal article
اللغة:	English
منشور في:	2003

مواد مشابهة

Myocardial dysfunction in hypertrophic cardiomyopathy.
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Ascertainment strategies and genotype:phenotype correlations in hypertrophic cardiomyopathy.
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Metabolic perturbations in the pathogenesis of hypertrophic cardiomyopathy
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The genetics of hypertrophic cardiomyopathy: Teare redux.
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Functional analysis of hypertrophic cardiomyopathy missense mutations in the light meromyosin region of beta myosin heavy chain
حسب: Redwood, C, وآخرون
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Inherited cardiomyopathies.
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منشور في: (2011)

Inherited cardiomyopathies.
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Disease pathways and novel therapeutic targets in hypertrophic cardiomyopathy.
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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.
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Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.
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Exercise-induced ventricular dysfunction in hypertrophic cardiomyopathy: stunning by any other name?
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Hypertrophic cardiomyopathy mutations in the gamma 2 subunit of AMP-activated kinase suggest a central role of energy compromise in disease pathogenesis
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Linked genetic modifiers in hypertrophic cardiomyopathy
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Correlates of myocardial fibrosis in hypertrophic cardiomyopathy
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Identification of myocardial disarray in patients with hypertrophic cardiomyopathy and ventricular arrhythmias
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Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
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Novel mutations in cardiac MYBPC3 causing early onset malignant hypertrophic cardiomyopathy
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Diffusion tensor magnetic resonance imaging of myocardial disarray in hypertrophic cardiomyopathy
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Is DNA testing for hypertrophic cardiomyopathy cost-effective?
حسب: Wordsworth, S, وآخرون
منشور في: (2006)

Mutations in cis can confound genotype-phenotype correlations in hypertrophic cardiomyopathy.
حسب: Blair, E, وآخرون
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Double mutations in CIS can confound genotype-phenotype correlations in hypertrophic cardiomyopathy
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Novel mutations in cardiac MYPBC3 cause early onset malignant hypertrophic cardiomyopathy (HCM)
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Progression of myocardial fibrosis in hypertrophic cardiomyopathy: mechanisms and clinical implications
حسب: Raman, B, وآخرون
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Blunted myocardial oxygenation response during vasodilator stress in patients with hypertrophic cardiomyopathy.
حسب: Karamitsos, T, وآخرون
منشور في: (2013)

METABOLIC ALTERATION IN HYPERTROPHIC CARDIOMYOPATHY (METAL-HCM STUDY): RANDOMISED DOUBLE BLINDED PLACEBO CONTROLLED TRIAL OF PERHEXILINE THERAPY IN PATIENT WITH HYPERTROPHIC CARDIOMYOPATHY
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Dilated and hypertrophic cardiomyopathy mutations in troponin and alpha-tropomyosin have opposing effects on the calcium affinity of cardiac thin filaments.
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Impaired left ventricular energy metabolism in hypertrophic cardiomyopathy is not due to fibrosis.
حسب: Petersen, SE, وآخرون
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حسب: Yu. V. Frolova, وآخرون
منشور في: (2017-02-01)

A novel mutation in phospholamban causes a mixed hypertrophic and dilated cardiomyopathy phenotype with autosomal dominant inheritance
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