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1
Genetic analysis of multifactorial cardiac diseases: idiopathic dilated cardiomyopathy and myocardial infarction
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Genetic analysis of multifactorial cardiac diseases: idiopathic dilated cardiomyopathy and myocardial infarction

Nihon Ika Daigaku zasshi, 1999, Vol.66 (5), p.332-335

ISSN: 0048-0444

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2
Surviving heart failure: Robert L. Frye lecture
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Surviving heart failure: Robert L. Frye lecture

Mayo Clinic proceedings, 2000, Vol.75 (1), p.111-118

ISSN: 0025-6196 ;EISSN: 1942-5546

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3
Genetic causes of inherited cardiac hypertrophy: Robert L. Frye Lecture
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Genetic causes of inherited cardiac hypertrophy: Robert L. Frye Lecture

Mayo Clinic proceedings, 2002, Vol.77 (12), p.1315-1319

ISSN: 0025-6196 ;EISSN: 1942-5546

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4
Dilated cardiomyopathy in the practice of a therapist and cardiologist (lecture)
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Dilated cardiomyopathy in the practice of a therapist and cardiologist (lecture)

Terapevticheskii arkhiv, 2004, Vol.76 (1), p.12-17

ISSN: 0040-3660

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5
Hypertensive cardiomyopathy in the practice of primary therapist and cardiologist (lecture)
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Hypertensive cardiomyopathy in the practice of primary therapist and cardiologist (lecture)

Terapevticheskii arkhiv, 2006, Vol.78 (1), p.28-35

ISSN: 0040-3660

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6
Profound hypocalcaemia presenting with a dilated cardiomyopathy and possible mitochondrial dysfunction in a 3 week old infant
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Profound hypocalcaemia presenting with a dilated cardiomyopathy and possible mitochondrial dysfunction in a 3 week old infant

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7
CMR of LV non-compaction cardiomyopathy: association of clinical presentation and prognosis with cardiac phenotype
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CMR of LV non-compaction cardiomyopathy: association of clinical presentation and prognosis with cardiac phenotype

DOI: 10.1186/1532-429X-13-S1-P291

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8
Electric channels, genetics and cardiac sudden death. Brugada syndrome as an example
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Electric channels, genetics and cardiac sudden death. Brugada syndrome as an example

Anales de la Real Academia Nacional de Medicina, 2012, Vol.129 (1), p.67-74

ISSN: 0034-0634

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9
Neovascularisation Potential of Blood Outgrowth Endothelial Cells From Patients With Severe Ischemic Cardiomyopathy
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Neovascularisation Potential of Blood Outgrowth Endothelial Cells From Patients With Severe Ischemic Cardiomyopathy

Circulation, 2013, Vol.128 (22)

ISSN: 0009-7322 ;EISSN: 1524-4539

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10
Prognostic value of cardiac fibrosis in patients with non-ischemic cardiomyopathy without congestive heart failure: a multicentre magnetic resonance study
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Prognostic value of cardiac fibrosis in patients with non-ischemic cardiomyopathy without congestive heart failure: a multicentre magnetic resonance study

European Heart Journal, 2014, Vol.35, p.870-871

ISSN: 0195-668X ;EISSN: 1522-9645

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11
GNE myopathy: a personal trip from bedside observation to therapeutic trials
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GNE myopathy: a personal trip from bedside observation to therapeutic trials

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2014, Vol.33 (2), p.107-110

ISSN: 1128-2460

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12
Proliferating myofibroblasts contribute to extracellular matrix remodeling in a porcine model of ischemic cardiomyopathy
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Proliferating myofibroblasts contribute to extracellular matrix remodeling in a porcine model of ischemic cardiomyopathy

European Heart Journal, 2015, Vol.36, p.952-953

ISSN: 0195-668X ;EISSN: 1522-9645

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13
Effects of Hypertrophic Cardiomyopathy Mutations on Myosin Structural Dynamics
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Effects of Hypertrophic Cardiomyopathy Mutations on Myosin Structural Dynamics

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14
Targeted capture sequencing identifies mutations in a substantial proportion of prior genotype negative - phenotype positive patients with inherited primary arrhythmia syndrome or cardiomyopathy
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Targeted capture sequencing identifies mutations in a substantial proportion of prior genotype negative - phenotype positive patients with inherited primary arrhythmia syndrome or cardiomyopathy

European Heart Journal. Supplements, 2015, Vol.36 (1), p.531-531

ISSN: 0195-668X ;EISSN: 1522-9645

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15
High agreement between a cardiology specific scoring system and the ACMG criteria for genetic variant interpretation and classification
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High agreement between a cardiology specific scoring system and the ACMG criteria for genetic variant interpretation and classification

Circulation, 2016, Vol.134

ISSN: 0009-7322 ;EISSN: 1524-4539

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16
Hepatocyte-specific SR-BI gene transfer corrects cardiac dysfunction in Scarb1-deficient mice and improves pressure overload-induced cardiomyopathy
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Hepatocyte-specific SR-BI gene transfer corrects cardiac dysfunction in Scarb1-deficient mice and improves pressure overload-induced cardiomyopathy

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2017, Vol.In press, p.259-260

ISSN: 1079-5642 ;EISSN: 1524-4636

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17
Hepatocyte-restricted SR-BI gene transfer corrects cardiac dysfunction in SR-BI deficient mice and improves pressure overload-induced cardiomyopathy
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Hepatocyte-restricted SR-BI gene transfer corrects cardiac dysfunction in SR-BI deficient mice and improves pressure overload-induced cardiomyopathy

European Heart Journal, 2017, Vol.38 (Supplement 1), p.259-260

ISSN: 0195-668X ;EISSN: 1522-9645

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18
Impact of Hypertrophic Cardiomyopathy Mutations on Myosin Catalytic ATPase Activity
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Impact of Hypertrophic Cardiomyopathy Mutations on Myosin Catalytic ATPase Activity

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19
Biventricular imaging markers to predict outcome in non-compaction cardiomyopathy: a machine learning study
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Biventricular imaging markers to predict outcome in non-compaction cardiomyopathy: a machine learning study

EUROPEAN HEART JOURNAL, 2018, Vol.39, p.1376-1377

ISSN: 0195-668X ;EISSN: 1522-9645

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20
HDL-targeted gene transfer and apo A-I nanoparticles for treatment of heart failure
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HDL-targeted gene transfer and apo A-I nanoparticles for treatment of heart failure

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Results 1 - 20 of 26  for All Library Resources

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