Works matching Cardiomyopathies
Results: 5000
Current use of cardiac magnetic resonance in tertiary referral centres for the diagnosis of cardiomyopathy: the ESC EORP Cardiomyopathy/Myocarditis Registry.
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- European Heart Journal - Cardiovascular Imaging, 2021, v. 22, n. 7, p. 781, doi. 10.1093/ehjci/jeaa329
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- Article
Cardiomyopathies in the Clinical Practice – an Overview.
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- Praxis (16618157), 2022, v. 111, n. 11, p. 623, doi. 10.1024/1661-8157/a003912
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- Article
MIECTOMIA SEPTAL E ABLAÇÃO SEPTAL ALCOÓLICA PARA CONTROLE CLÍNICO DE PACIENTES COM CARDIOMIOPATIA HIPERTRÓFICA OBSTRUTIVA: UMA REVISÃO INTEGRATIVA.
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- Revista Foco (Interdisciplinary Studies Journal), 2024, v. 17, n. 3, p. 1, doi. 10.54751/revistafoco.v17n3-133
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- Article
CARDIOMIOPATIA DE TAKOTSUBO: DIFERENÇA SOBRE A INCIDÊNCIA ENTRE AS MULHERES NA PÓS-MENOPAUSA E MULHERES FÉRTEIS.
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- Revista Foco (Interdisciplinary Studies Journal), 2023, v. 16, n. 10, p. 1, doi. 10.54751/revistafoco.v16n10-061
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- Article
An unusual case of severe left ventricle outflow tract obstruction due to a coexistence of Takotsubo cardiomyopathy with septal hypertrophic cardiomyopathy.
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- Monaldi Archives for Chest Disease, 2022, v. 92, n. 3, p. 1, doi. 10.4081/monaldi.2021.2106
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- Article
Evolutionary Change Mimicking Apical Hypertrophic Cardiomyopathy in a Patient with Takotsubo Cardiomyopathy.
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- Echocardiography, 2014, v. 31, n. 10, p. E293, doi. 10.1111/echo.12722
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- Article
Reverse Takotsubo Cardiomyopathy in a Patient With Prior Apical Takotsubo Cardiomyopathy: Challenging the Beta Receptor Gradient Theory.
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- Ochsner Journal, 2019, v. 19, n. 3, p. 256, doi. 10.31486/toj.18.0027
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- Article
Clinical features differentiating Takotsubo cardiomyopathy in the peripartum period from peripartum cardiomyopathy.
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- Heart & Vessels, 2020, v. 35, n. 5, p. 665, doi. 10.1007/s00380-019-01537-4
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- Article
Metabolic Processes are Potential Biological Processes Distinguishing Nonischemic Dilated Cardiomyopathy from Ischemic Cardiomyopathy: A Clue from Serum Proteomics.
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- Pharmacogenomics & Personalized Medicine, 2021, v. 14, p. 1169, doi. 10.2147/PGPM.S323379
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- Article
2023 ESC Guidelines for the management of cardiomyopathies: Developed by the task force on the management of cardiomyopathies of the European Society of Cardiology (ESC).
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- European Heart Journal, 2023, v. 44, n. 37, p. 3503, doi. 10.1093/eurheartj/ehad194
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- Article
A dynamic variant of Takotsubo cardiomyopathy mimicking apical hypertrophic cardiomyopathy: a case report.
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- 2025
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- Case Study
Hypertrophic Cardiomyopathy and Primary Restrictive Cardiomyopathy: Similarities, Differences and Phenocopies.
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- Journal of Clinical Medicine, 2021, v. 10, n. 9, p. 1954, doi. 10.3390/jcm10091954
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- Article
Basal wall hypercontraction of Takotsubo cardiomyopathy in a patient who had been diagnosed with dilated cardiomyopathy: a case report.
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- 2017
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- Publication type:
- journal article
Phospholamban R14del mutation in patients diagnosed with dilated cardiomyopathy or arrhythmogenic right ventricular cardiomyopathy: evidence supporting the concept of arrhythmogenic cardiomyopathy.
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- European Journal of Heart Failure, 2012, v. 14, n. 11, p. 1199, doi. 10.1093/eurjhf/hfs119
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- Article
Analysis of Associated Genes and Biological Pathways Between Inflammatory Dilated Cardiomyopathy and Ischemic Cardiomyopathy by Bioinformatics.
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- E Journal of Cardiovascular Medicine, 2023, v. 11, n. 1, p. 31, doi. 10.32596/ejcm.galenos.2023.2022-12-054
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- Article
Peripartum cardiomyopathy and dilated cardiomyopathy: different at heart.
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- Frontiers in Physiology, 2015, v. 5, p. 1, doi. 10.3389/fphys.2014.00531
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- Article
CORRELATION BETWEEN E/VP AND E/E' IN LEFT VENTRICULAR FILLING PRESSURE MEASUREMENT AMONG PATIENTS WITH DILATED CARDIOMYOPATHY.
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- Folia Medica Indonesiana, 2014, v. 50, n. 1, p. 30
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- Article
Quality of life status determinants in hypertrophic cardiomyopathy as evaluated by the Kansas City Cardiomyopathy Questionnaire.
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- 2020
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- journal article
Fetal Echocardiography is Useful for Screening Fetuses with a Family History of Cardiomyopathy.
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- Pediatric Cardiology, 2020, v. 41, n. 8, p. 1766, doi. 10.1007/s00246-020-02439-3
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- Article
Comparison of Immune Profiles in Fetal Hearts with Idiopathic Dilated Cardiomyopathy, Maternal Autoimmune-Associated Dilated Cardiomyopathy and the Normal Fetus.
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- Pediatric Cardiology, 2016, v. 37, n. 2, p. 353, doi. 10.1007/s00246-015-1284-4
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- Article
Overview of the 2023 ESC guidelines for the management of cardiomyopathies.
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- Heart, Vessels & Transplantation, 2023, v. 7, n. 4, p. 1, doi. 10.24969/hvt.2023.440
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- Article
Kardiomiopatie w populacji pacjentów pediatrycznych.
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- Family Medicine Forum / Forum Medycyny Rodzinnej, 2023, v. 17, n. 2, p. 73
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- Article
Advanced Computed Tomography and Magnetic Resonance Imaging in Ischemic and Nonischemic Cardiomyopathies.
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- Echocardiography, 2025, v. 42, n. 2, p. 1, doi. 10.1111/echo.70106
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- Article
Distinct Circulating Expression Profiles of Long Noncoding RNAs in Heart Failure Patients With Ischemic and Nonischemic Dilated Cardiomyopathy.
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- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01116
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- Article
Pathological findings in apical hypertrophic cardiomyopathy: an indication for orthotopic heart transplantation – Case Report
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- Indian Journal of Transplantation, 2009, v. 3, p. 17, doi. 10.1016/S2212-0017(11)60089-0
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- Article
Two Cases of Apical Ballooning Syndrome Masking Apical Hypertrophic Cardiomyopathy.
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- Texas Heart Institute Journal, 2014, v. 41, n. 2, p. 179, doi. 10.14503/THIJ-13-3191
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- Article
Incidence and Impact of Myocarditis in Genetic Cardiomyopathies: Inflammation as a Potential Therapeutic Target.
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- Genes, 2025, v. 16, n. 1, p. 51, doi. 10.3390/genes16010051
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- Article
Identification of Two Homozygous Variants in MYBPC3 and SMYD1 Genes Associated with Severe Infantile Cardiomyopathy.
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- Genes, 2023, v. 14, n. 3, p. 659, doi. 10.3390/genes14030659
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- Article
Genetic Insights from Consanguineous Cardiomyopathy Families.
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- Genes, 2023, v. 14, n. 1, p. 182, doi. 10.3390/genes14010182
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- Article
Genetics of Peripartum Cardiomyopathy: Current Knowledge, Future Directions and Clinical Implications.
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- Genes, 2021, v. 12, n. 1, p. 103, doi. 10.3390/genes12010103
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- Article
Stress-induced cardiomyopathy (Takotsubo) - broken heart and mind?
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- Vascular Health & Risk Management, 2013, v. 9, p. 149, doi. 10.2147/VHRM.S40163
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- Article
Beyond hypertrophic cardiomyopathy: unmasking alternative causes of LVOT obstruction on CMR.
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- International Journal of Cardiovascular Imaging, 2025, v. 41, n. 2, p. 387, doi. 10.1007/s10554-024-03311-8
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- Article
Prevalence and clinical correlates of ascending aortic dilatation in patients with noncompaction cardiomyopathy.
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- International Journal of Cardiovascular Imaging, 2023, v. 39, n. 9, p. 1687, doi. 10.1007/s10554-023-02882-2
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- Article
Dilated Cardiomyopathy: A Genetic Journey from Past to Future.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 21, p. 11460, doi. 10.3390/ijms252111460
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- Article
DSP -Related Cardiomyopathy as a Distinct Clinical Entity? Emerging Evidence from an Italian Cohort.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2490, doi. 10.3390/ijms24032490
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- Article
Recent Findings Related to Cardiomyopathy and Genetics.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 22, p. 12522, doi. 10.3390/ijms222212522
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- Article
Cardiomyopathies: An Overview.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 14, p. 7722, doi. 10.3390/ijms22147722
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- Article
Genetic Restrictive Cardiomyopathy: Causes and Consequences—An Integrative Approach.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 2, p. 558, doi. 10.3390/ijms22020558
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- Article
Direct Sarcomere Modulators Are Promising New Treatments for Cardiomyopathies.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 1, p. 226, doi. 10.3390/ijms21010226
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- Article
Cardiac Sarcoidosis and Inherited Cardiomyopathies: Clinical Masquerade or Overlap?
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- Journal of Clinical Medicine, 2025, v. 14, n. 5, p. 1609, doi. 10.3390/jcm14051609
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- Article
Recommendations for the Management of Cardiomyopathy Mutation Carriers: Evidence, Doubts, and Intentions.
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- Journal of Clinical Medicine, 2023, v. 12, n. 14, p. 4706, doi. 10.3390/jcm12144706
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- Article
Cardiac Sarcoid: A Chameleon Masquerading as Hypertrophic Cardiomyopathy and Dilated Cardiomyopathy in the Same Patient.
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- Echocardiography, 2014, v. 31, n. 5, p. E138, doi. 10.1111/echo.12536
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- Article
TCAP gene is not a common cause of cardiomyopathy in Iranian patients.
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- European Journal of Medical Research, 2023, v. 28, n. 1, p. 1, doi. 10.1186/s40001-023-01019-4
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- Article
Kardiomiopatia tachyarytmiczna - ważny i niedoceniany problem kliniczny.
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- Polish Journal of Cardiology / Polski Przeglad Kardiologiczny, 2012, v. 14, n. 3, p. 213
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- Article
Adriamycin-induced cardiomyopathy can serve as a model for diabetic cardiomyopathy – a hypothesis.
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- Asian Pacific Journal of Tropical Biomedicine, 2017, v. 7, n. 11, p. 1041, doi. 10.1016/j.apjtb.2017.09.021
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- Article
Cardiac Proteome Profiling in Ischemic and Dilated Cardiomyopathy Mouse Models.
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- Frontiers in Physiology, 2019, p. N.PAG, doi. 10.3389/fphys.2019.00750
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- Article
Predictive Factors for Catecholamine-Induced Cardiomyopathy in Patients with Pheochromocytoma and Paraganglioma.
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- Frontiers in Endocrinology, 2022, v. 13, p. 1, doi. 10.3389/fendo.2022.853878
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- Article
Dilated cardiomyopathy due to hypocalcaemia: a case report.
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- 2024
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- Case Study
Childhood Cardiomyopathies: A Study in Tertiary Care Hospital in Upper Egypt.
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- Electronic Physician, 2016, v. 8, n. 11, p. 3164, doi. 10.19082/3164
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- Article
DSP p.(Thr2104Glnfs*12) variant presents variably with early onset severe arrhythmias and left ventricular cardiomyopathy.
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- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-0955-z
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- Article