Clinical burden of obstructive hypertrophic cardiomyopathy in France by Philippe Charron, Carla Zema, François-Emery Cotté, Eléonore Herquelot, Taryn Krause, Florent Daydé, Jean-Noël Trochu

Subjects: “…hypertrophic cardiomyopathy…”
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Hypertrophic cardiomyopathy with mid-ventricular obstruction and apical aneurysm by N.D. Oryshchyn, Yu.A. Ivaniv, Yu.H. Kyjak, S.S. Pavlyk, V.S. Moroz, D.I. Besh, I.M. Bigun

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An Unusual Presentation of a Myocardial Crypt in Hypertrophic Cardiomyopathy by Danny A. J. P. van de Sande, Jan Hoogsteen, Luc J. H. J. Theunissen

“…Hypertrophic cardiomyopathy (HCM) is a common inherited cardiovascular disease with prevalence of 0.2% in the population. …”
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The results of alcoholic septal ablation in the treatment of hypertrophic cardiomyopathy by B.M. Todurov, G.I. Kovtun, A.V. Khokhlov, O.V. Pantazi, A.O. Shpachuk, A.Yu. Melnik, A.O. Maksakov, A.S. Batsiun

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Research Progress of Perioperative Anesthesia Management in Patients with Hypertrophic Cardiomyopathy by LIN Shuantong, SU Xiaojun, CAO Dequan

Subjects: “…hypertrophic cardiomyopathy…”
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Hyaluronan and Collagen in Human Hypertrophic Cardiomyopathy: A Morphological Analysis by Martin Hellström, Anna Engström-Laurent, Stellan Mörner, Bengt Johansson

“…Introduction. The hypertrophic cardiomyopathy (HCM) disease process is not only limited to cardiomyocyte abnormalities but also engages the extracellular matrix. …”
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MEASLES WITH THE COMPLICATION OF NON-OBSTRUCTIVE HYPERTROPHIC CARDIOMYOPATHY; CASE REPORT by Ramna Shafique Rafique, Saleha Haider, Maria Kanwal, Saba Safdar, Tayyaba Anwar, Zain Yousaf Ally

“…We present a case of a 6-month-old girl who came with measles-like symptoms and later developed complications of non-obstructive hypertrophic cardiomyopathy. …”
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Clinical Implications of Pan-Immune-inflammatory Values in Patients with Hypertrophic Cardiomyopathy by Levent PAY, Ahmet Cagdas YUMURTAS, Seyda DERELI, Tugba CETIN, Hikmet KADI, Tufan CINAR, Mert Ilker HAYIROGLU

Subjects: “…hypertrophic cardiomyopathy…”
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Serum biochemical profile in case of cardiorenal syndrome in cats with hypertrophic cardiomyopathy by Yu. A. Vatnikov, E. D. Sotnikova, V. I. Kuznetsov, A. A. Razumova, I. V. Shchurov, O. A. Petrukhina, A. A. Rudenko

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Role of Cardiac Magnetic Resonance in Detecting Biventricular Apical Hypertrophic Cardiomyopathy by Nathan Zaher, Hammam Shereef, Rashid Al Hussain, John Dawdy, Diane Levine, M. Chadi Alraies

“…Apical Hypertrophic Cardiomyopathy (ApHCM) is a rare variant of hypertrophic cardiomyopathy with a low prevalence in the general population. …”
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Serial Observations and Mutational Analysis of an Adoptee with Family History of Hypertrophic Cardiomyopathy by Bronwyn Harris, Jean P. Pfotenhauer, Cheri A. Silverstein, Larry W. Markham, Kim Schafer, Vernat J. Exil, Charles C. Hong

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Pediatric hypertrophic cardiomyopathy caused by a novel TNNI3 variant by Natsuko Inagaki, Tomoya Okano, Masatake Kobayashi, Masatsune Fujii, Yoshinao Yazaki, Yasuyoshi Takei, Hisanori Kosuge, Shinji Suzuki, Takeharu Hayashi, Masahiko Kuroda, Kazuhiro Satomi

“…Abstract TNNI3 is a gene that causes hypertrophic cardiomyopathy (HCM). A 14-year-old girl who was diagnosed with nonobstructive HCM presented with cardiopulmonary arrest due to ventricular fibrillation. …”
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Contribution of hypoxia-inducible factor 1alpha to pathogenesis of sarcomeric hypertrophic cardiomyopathy by Sarala Raj Murthi, Andreas Petry, Bachuki Shashikadze, Jan B. Stöckl, Manuel Schmid, Gianluca Santamaria, Karin Klingel, Damir Kračun, Xinpei Chen, Sabine Bauer, Joachim P. Schmitt, Florian Flenkenthaler, Josh Gorham, Christopher N. Toepfer, David Potěšil, Pavel Hruška, Zbyněk Zdráhal, Zsuzsanna Mayer, Mathieu Klop, Luisa Lehmann, Yishi Qin, Laura Papanakli, Nadine Spielmann, Alessandra Moretti, Thomas Fröhlich, Peter Ewert, Stefan Holdenrieder, Jonathan G. Seidman, Christine E. Seidman, Agnes Görlach, Cordula M. Wolf

Subjects: “…Hypertrophic cardiomyopathy…”
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Refractory cardiogenic shock in hypertrophic cardiomyopathy complicated by apical ballooning: A case report by Matej Strycek, Rostislav Polasek, Pavol Tomasov, Jiri Karasek

“…Hypertrophic cardiomyopathy can be accompanied by dynamic obstruction in the left ventricular outflow tract and acute apical ballooning, which are among the very rare causes of cardiogenic shock. …”
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Hypertrophic Cardiomyopathy Mimicking Acute Anterior Myocardial Infarction Associated with Sudden Cardiac Death by Y. Daralammouri, M. El Garhy, K. Same, B. Lauer

“…Hypertrophic cardiomyopathy is the most common genetic disease of the heart. …”
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PET-CT Imaging in Hypertrophic Cardiomyopathy: A Narrative Review on Risk Stratification and Prognosis by Patrícia Marques-Alves, Lino Gonçalves, Maria João Ferreira

Subjects: “…hypertrophic cardiomyopathy…”
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Effects of genetic mutations on left ventricular myocardial mechanics and fibrosis patterns in hypertrophic cardiomyopathy by Minjeong Kim, Yoonjung Kim, Hyemoon Chung, Jiwon Seo, Chul Hwan Park, Tae Hoon Kim, Se-Joong Rim, Kyung-A Lee, Eui-Young Choi

Subjects: “…Hypertrophic cardiomyopathy…”
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Efficacy of Novel Noncontrast Cardiac Magnetic Resonance Methods in Indicating Fibrosis in Hypertrophic Cardiomyopathy by Maedeh Sharifian, Nahid Rezaeian, Sanaz Asadian, Ali Mohammadzadeh, Ali Nahardani, Kianosh Kasani, Yaser Toloueitabar, Ali Mohammad Farahmand, Leila Hosseini

“…Objective. In hypertrophic cardiomyopathy (HCM), myocardial fibrosis is routinely shown by late gadolinium enhancement (LGE) in cardiac magnetic resonance (CMR) imaging. …”
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Systemic Lupus Erythematosus Complicated with Hypertrophic Cardiomyopathy: A Case Report and Literature Review by Huihui Ma, Xin Cao, Jing Zhang, Yongmei Zhou, Rong Luo, Tao He, Jianhong Tao, Xiaoping Li

“…A 32-year-old female with systemic lupus erythematosus (SLE) for more than 7 years, and long-term treatment with cyclophosphamide, cyclosporine, methotrexate, and tacrolimus, later found to be combined with hypertrophic cardiomyopathy (HCM) for one year. The patient denied a family history of cardiomyopathy and sudden cardiac death (SCD). …”
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Mitochondrial Cardiomyopathy Presenting as Dilated Phase of Hypertrophic Cardiomyopathy Diagnosed with Histological and Genetic Analyses by Toshiki Kuno, Syohei Imaeda, Yohei Asakawa, Hiroshi Nakamura, Genzou Takemura, Daisuke Asahara, Akira Kanamori, Tomoyuki Kabutoya, Yohei Numasawa

“…We report a case with 46-year-old man diagnosed with mitochondrial cardiomyopathy in the dilated phase of hypertrophic cardiomyopathy. Since cardiac magnetic resonance imaging, beta-methyl-p-I123-iodophenyl-pentadecanoic myocardial scintigraphy, and positron emission tomography/computed tomography revealed no remarkable findings, we performed electron microscopic examination, which aided in diagnosing mitochondrial cardiomyopathy. …”
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