scholarly article | Q13442814 |
P50 | author | Naoki Nishida | Q44537420 |
P2093 | author name string | Yoshiaki Yamaguchi | |
Yuko Oku | |||
Fukiko Ichida | |||
Keiichi Hirono | |||
Yukiko Hata | |||
Shojiro Ichimata | |||
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Prognostic predictive value of gene mutations in Japanese patients with hypertrophic cardiomyopathy | Q33167938 | ||
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome | Q33603766 | ||
Hypertrophic cardiomyopathy without hypertrophy: two families with myocardial disarray in the absence of increased myocardial mass | Q33610845 | ||
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing | Q33655317 | ||
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Occurrence and Frequency of Arrhythmias in Hypertrophic Cardiomyopathy in Relation to Delayed Enhancement on Cardiovascular Magnetic Resonance | Q57418111 | ||
Hypertrophic nonobstructive cardiomyopathy with giant negative T waves (apical hypertrophy): Ventriculographic and echocardiographic features in 30 patients | Q67019025 | ||
Relation between extent of cardiac muscle cell disorganization and left ventricular wall thickness in hypertrophic cardiomyopathy | Q68037630 | ||
Progression of hypertrophic cardiomyopathy into a hypokinetic left ventricle: higher incidence in patients with midventricular obstruction | Q69726380 | ||
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Lack of Phenotypic Differences by Cardiovascular Magnetic Resonance Imaging in MYH7 (β-Myosin Heavy Chain)- Versus MYBPC3 (Myosin-Binding Protein C)-Related Hypertrophic Cardiomyopathy | Q38963414 | ||
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Muscle fiber disarray in common heart diseases | Q39827177 | ||
Angled aorta ("sigmoid septum") as a cause of hypertrophic subaortic stenosis | Q39861036 | ||
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Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy. | Q41237982 | ||
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Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series | Q42503963 | ||
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy | Q42515078 | ||
Echocardiographic risk factors predisposing to sudden cardiac death in hypertrophic cardiomyopathy | Q43013040 | ||
Clinical course of hypertrophic cardiomyopathy in a regional United States cohort | Q43565120 | ||
Quantitative analysis of cardiac muscle cell disorganization in the ventricular septum. Comparison of fetuses and infants with and without congenital heart disease and patients with hypertrophic cardiomyopathy | Q44063544 | ||
Quantitative analysis of cardiac muscle cell disorganization in the ventricular septum of patients with hypertrophic cardiomyopathy | Q44134258 | ||
Myocardial disarray at junction of ventricular septum and left and right ventricular free walls in hypertrophic cardiomyopathy | Q44423917 | ||
Hypertrophic cardiomyopathy clinical phenotype is independent of gene mutation and mutation dosage | Q45339581 | ||
Association of common genetic variants related to atrial fibrillation and the risk of ventricular fibrillation in the setting of first ST-elevation myocardial infarction. | Q47826134 | ||
Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene | Q47957734 | ||
Clinical Characteristics and Long-Term Outcome of Hypertrophic Cardiomyopathy in Individuals With a MYBPC3 (Myosin-Binding Protein C) Founder Mutation. | Q47971514 | ||
Pathological features of preclinical or early clinical stages of corticobasal degeneration: a comparison with advanced cases | Q48313740 | ||
Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing | Q48775549 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 4 | |
P577 | publication date | 2019-04-05 | |
P1433 | published in | Journal of Clinical Medicine | Q27724774 |
P1476 | title | Clinicopathological and Genetic Profiles of Cases with Myocytes Disarray-Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy. | |
P478 | volume | 8 |
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