Restrictive cardiomyopathy: difficulties desminopathy diagnostics by T. G. Vaikhanskaya, T. M. Kaptsiukh, T. V. Kurushko, L. N. Sivitskaya, O. D. Liaudanski, N. G. Danilenko

Subjects: “…restrictive cardiomyopathy…”
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Molecular genetic features of the development of restrictive cardiomyopathy in Russian children by K. V. Savostyanov, E. N. Basargina, E. E. Ryabova, A. A. Pushkov, I. S. Zhanin, E. Yu. Basargina, A. Yu. Alekseeva, L. V. Muraveva, L. A. Gandaeva, A. P. Fisenko

Subjects: “…restrictive cardiomyopathy…”
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The MYH7 c.2770G > A (p.Glu924Lys) mutation exhibits phenotypic heterogeneity in hypertrophic cardiomyopathy (HCM) and restrictive cardiomyopathy (RCM): a case report by Yuanyuan Han, Haiyang Wang, Hongsheng Zhang, Manman Wang, Lijun Gan, Fanhua Meng

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Cardiomyopathy with Restrictive-Hypertrophic Phenotype and Initial Morphological Diagnosis “Amyloidosis” as a Manifestation of Danon Disease in a Woman by O. V. Blagova, E. A. Kogan, V. P. Sedov, Yu. A. Lutokhina, A. V. Nedostup, A. V. Ott, L. M. Dashinemaeva, E. V. Zaklyazminskaya

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The clinical case of cardiac amyloidosis associated with multiple myeloma by E. I. Tsoi, Yu. V. Rogovskaya, S. V. Demyanov, V. V. Ryabov

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Clinical profile of restrictive cardiomyopathy in children at a South Indian tertiary care cardiac center: A retrospective three decade experience by Gousia Mukhtar Kawoos, Arun Gopalakrishnan, Kavassery Mahadevan Krishnamoorthy, Bijulal Sasidharan, Harikrishnan K. N. Kurup, P. Sankara Sarma, Narayanan Namboodiri, Harikrishnan Sivadasanpillai

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Register of adult patients with noncompact left ventricular myocardium: classification of clinical forms and a prospective assessment of progression by E. V. Pavlenko, O. V. Blagova, N. V. Varionchik, A. V. Nedostup, V. P. Sedov, M. E. Polyak, E. V. Zaklyazminskaya

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Systemic amyloidosis in a patient with acute heart failure by E. V. Shekhovtsova, E. V. Lukashik, O. A. Bogochanova, M. S. Kolonutov, M. A. Kudinova, E. V. Reznik

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The diagnostic yield of non-invasive testing features in cardiac amyloidosis by Domagoj Kustić, Josipa Vukšić, Dražen Huić

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Evolution of clinical and genetic concepts of cardiomyopathies by O.M. Kovalyova, V.V. Nikonov, S.V. Ivanchenko, A.M. Litvynova, T.I. Viun, O.M. Fedota

“…The diagnostic value of structural and functional heart anomalies for ranking classical phenotypes of dilated, hypertrophic, restrictive cardiomyopathies, and arrhythmogenic right ventricular cardiomyopathy is аnalyzed. …”
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Prognostic model for the development of cardiomyopathies based on genetic predictors by S. Yu. Nikulina, O. O. Kuznetsova, G. V. Matyushin, A. A. Chernova, V. N. Maksimov

“…To develop a prognostic model for the development of primary and secondary cardiomyopathy based on genetic predictors.Material and methods. …”
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Predictors of heart failure in patients with cardiomyopathies of various origins by O. O. Kuznetsova, S. Yu. Nikulina, G. V. Matyushin, A. A. Chernova, V. A. Sakovich, V. N. Maksimov

“…To identify predictors of heart failure in patients with dilated cardiomyopathy (DCM) and ischemic myocardial dilatation (IMD).Material and methods. …”
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Systemic ATTR-amyloidosis, a Rare Form of Internal Organ Damage by V. V. Rameev, R. P. Myasnikov, P. P. Vinogradov, L. V. Kozlovskaya, S. V. Moiseev, E. I. Fomicheva, S. A. Beregovskaya, E. A. Mershina, S. A. Kostina, L. A. Strizhakov, A. S. Rameeva, P. P. Tao, O. M. Drapkina

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LEFT VENTRICULAR WALL THICKNESS AND AUTONOMIC REGULATION IN PATIENTS WITH HYPERTROPHIC CARDIOMYOPATHY by O. Allaberganov, T. A. Abdullaev, G. A. Nagaeva

“…The study included 21 patients (mean age 35,86±10,01 years) with hypertrophic cardiomyopathy (HCMP) diagnosed according to the WHO criteria. …”
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Prognostic significance of FT3 levels in hypertrophic cardiomyopathy patients with HFpEF by Zhen-Yu Yang, Zhi-Yuan Zhang, Wei-Jie Zhang, Da Liu, Fu-Shi Piao, Xiangyu Yan, Fang-Tao Shi, Min Yang, Jing Chen, Sheng-song Zhu, Hong-Hou He, Pei-Hong Wu, Cheng Qian, Min Lin, Jun-Qing Feng, Chun-jin Lai

“…ObjectiveThis study sought to identify key prognostic factors in patients with hypertrophic cardiomyopathy (HCM) and heart failure with preserved ejection fraction (HFpEF), emphasizing the prognostic role of free triiodothyronine (FT3) levels.Research design and methodsThis retrospective cohort study enrolled 992 HCM-HFpEF patients from two Chinese medical centers between 2009 and 2019, excluding those with thyroid-affecting medications or disorders. …”
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Massive tuberculous exudative pericarditis under the guise of hydropericardium in a patient with non-compaction cardiomyopathy: diagnosis and treatment by O. V. Blagova, I. N. Alieva, P. V. Senchikhin, L. D. Nazarova, S. V. Chernyavsky, G. Yu. Sorokin, E. V. Pavlenko, V. P. Sedov, N. V. Gagarina, N. D. Sarkisova

“…The first presentation of the combination of non-compaction cardiomyopathy  with a restrictive-dilated phenotype  and massive chronic tuberculous pericarditis, which for a long time was under  the guise  of hydropericardium  in congestive  heart  failure in a patient of 30 years, is performed. …”
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Troponin I – a comprehensive review of its function, structure, evolution, and role in muscle diseases by Dongju Han, Younghyun Lim, Soah Lee, Seong-il Eyun

“…Specifically, several mutations in cardiac troponin I have been linked to cardiomyopathies, such as hypertrophic, dilated, and restrictive cardiomyopathies, which affect heart contractility and calcium handling. …”
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INTRACORONARY AUTOLOGOUS BONE MARROW STEM CELL THERAPY IN DIASTOLIC HEART FAILURE by V. I. Shumakov, E. N. Ostroumov, T. V. Gubenko, A. Temnov, S. V. Gureev, N. A. Onishchenko, V. S. Suskova, N. N. Abramova, E. N. Kazakov

“…Due to ineffective therapy and increased dyspnoea, radionuclide ventriculography was performed, suggesting restrictive cardiomyopathy. Intracoronary injection of autologous bone marrow stem cells was performed. …”
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Parasitic infections and the development of endomyocardial fibrosis: systematic review of case reports and case series by Abel Aizeque, Alex Mwangi Kihunyu, Olamide Daniel Odusola, Sulymon A. Saka, Abdinasir Mohamed Aray

“…Abstract Background Endomyocardial fibrosis (EMF) is a chronic restrictive cardiomyopathy prevalent in tropical regions, often underdiagnosed and associated with poor outcomes. …”
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From hypertension to heart failure: The missed clues of transthyretin cardiac amyloidosis by Ambreen Gul, Kamran Dawood

“…Repeat echocardiography revealed severe LVH with a restrictive filling pattern, raising suspicion of an infiltrative cardiomyopathy, such as cardiac amyloidosis. …”
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