Showing 41 - 60 results of 69 for search '"hypertrophic cardiomyopathy"', query time: 0.05s Refine Results
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    A Case Series on Cardiac and Skeletal Involvement in Two Families with PRKAG2 Mutations by Anita Sri, Piers Daubeney, Sanjay Prasad, John Baksi, Maria Kinali, Inga Voges

    Published 2019-01-01
    “…PRKAG2 is a rare autosomal dominant syndrome that mainly presents with hypertrophic cardiomyopathy, ventricular preexcitation, and conduction abnormalities. …”
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    Article
  6. 46

    Case Report: A rare case of Noonan syndrome with multiple lentigines manifesting as cardiac enlargement by Linghua Fan, Jie Jiang, Yan Zhang, Xiaoning Han, Wenhui Ding, Xiaodi Xue, Yimeng Jiang

    Published 2025-01-01
    “…Characterized by multiple lentigines, hypertelorism, short stature, and hearing loss, its common cardiac manifestations include pulmonary stenosis, hypertrophic cardiomyopathy (HCM), atrial septal defect, and left-sided heart lesions. …”
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  7. 47

    Automated electronic health record-based screening for Fabry disease in unexplained left ventricular hypertrophy (FAPREV-HCM) by Christoph Wanner, Peter Nordbeck, Lora Lorenz, Nurcan Üçeyler, Claudia Sommer, Kolja Lau, Victoria Sokalski, Georg Fette

    Published 2025-01-01
    “…Background and aims Hypertrophic cardiomyopathy (HCM) has various aetiologies, including genetic conditions like Fabry disease (FD), a lysosomal storage disorder. …”
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    Article
  8. 48

    Triple Threat: Significant Concomitant Aortic Stenosis, Mitral Stenosis, and Systolic Anterior Motion of the Mitral Valve Causing Left Ventricular Outflow Tract Obstruction in Card... by Katelyn Glines, J. W. Awori Hayanga, Christina Gibson, Mohamad El Churafa, Lawrence Wei, Heather K. Hayanga

    Published 2023-01-01
    “…While SAM is typically observed in patients with hypertrophic cardiomyopathy or following mitral valve repair, it may be seen in any setting in which the anatomy and function of the left ventricle has been altered. …”
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    Article
  9. 49

    Early Renal Involvement in a Girl with Classic Fabry Disease by Fernando Perretta, Norberto Antongiovanni, Sebastián Jaurretche

    Published 2017-01-01
    “…Typical acroparesthesia in hands and feet, gastrointestinal symptoms, angiokeratomas, dyshidrosis, hearing loss, arrhythmias, hypertrophic cardiomyopathy, cerebrovascular accidents, and renal failure can be observed. …”
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    Article
  10. 50

    Anesthesia Management in Scoliosis Surgery of Patients with Friedreich’s Ataxia: A Report of Four Cases by Muhammed Köse, Ercan Bal, Şemsi Mustafa Aksoy, Ayşe Lafçı

    Published 2022-12-01
    “…Neuromuscular blocker was used for anesthesia induction in one case, we did not use it in the other cases. Hypertrophic cardiomyopathy may accompany patients with Friedreich's ataxia. …”
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    Article
  11. 51

    Hypertrophic Obstructive Cardiomyopathy Masked by Tako-Tsubo Syndrome: A Case Report by Y. Daralammori, M. El Garhy, M. R. Gayed, A. Farah, B. Lauer, M. A. Secknus

    Published 2012-01-01
    “…A 70-year-old female presented with Tako-tsubo cardiomyopathy and masked obstructive hypertrophic cardiomyopathy at presentation. Conclusion. Tako-tsubo cardiomyopathy typically presents like an acute MI and is characterized by severe, but transient, regional left ventricular systolic dysfunction. …”
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  12. 52

    T2-Weighted Cardiac Magnetic Resonance Imaging of Edema in Myocardial Diseases by Yasuo Amano, Masaki Tachi, Hitomi Tani, Kyoichi Mizuno, Yasuhiro Kobayashi, Shinichiro Kumita

    Published 2012-01-01
    “…In acute myocardial diseases, such as acute myocardial infarction and myocarditis, the edema is larger than myocardial scarring, whereas the edema can be smaller than the scarring in some types of nonischemic cardiomyopathy, including hypertrophic cardiomyopathy. T2-weighted MRI of edema identifies myocardial edema associated with ischemia, inflammation, vasculitis, or intervention in the myocardium and provides information complementary to delayed-enhancement MRI.…”
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  13. 53

    Features and Outcomes In Utero and after Birth of Fetuses with Myocardial Disease by Vlasta Fesslova, Maurizio Mongiovì, Salvatore Pipitone, Jelena Brankovic, Laura Villa

    Published 2010-01-01
    “…Ninety-one fetuses with dilated or hypertrophic cardiomyopathy (DCM, HCM) and myocarditis were studied. …”
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  14. 54

    Prevalence of Isolated Atrial Amyloidosis in Young Patients Affected by Congestive Heart Failure by Lia Millucci, Lorenzo Ghezzi, Giulia Bernardini, Daniela Braconi, Piero Tanganelli, Annalisa Santucci

    Published 2012-01-01
    “…We provide here the microscopic examination of atrial biopsies from 36 young (mean 40 years) CHF patients distinguished in idiopathic dilated cardiomyopathy (DC) affected and hypertrophic Cardiomyopathy (HC) affected, endorsing the presumptive association of early CHF with IAA. …”
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  15. 55

    Identification of novel genetic variants associated with feline cardiomyopathy using targeted next-generation sequencing by Jade Raffle, Jose Novo Matos, Marsha Wallace, Lois Wilkie, Richard J. Piercy, Perry Elliott, David J. Connolly, Virginia Luis Fuentes, Androniki Psifidi

    Published 2025-01-01
    “…This study aimed to identify novel genetic variants in cats with hypertrophic cardiomyopathy (HCM) and restrictive cardiomyopathy (RCM) using a targeted panel of genes associated with human cardiomyopathy. …”
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  16. 56

    Global Longitudinal Strain May Be the One that Appropriately Identifies Candidates of ICD Implantation by Mohammad Hossein Nikoo, Mohammad Zarrabi, Alireza Moaref, Iman Razeghian-Jahromi

    Published 2024-01-01
    “…Hypertrophic cardiomyopathy (HCM) significantly contributes to an elevated risk of sudden cardiac death. …”
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  17. 57

    Transient Ischemic Attack and Ischemic Stroke in Danon Disease with Formation of Left Ventricular Apical Thrombus despite Normal Systolic Function by Takeshi Tsuda, Amanda J. Shillingford, Jane Vetter, Vinay Kandula, Badal Jain, Joel Temple

    Published 2017-01-01
    “…Danon disease is a rare X-linked dominant skeletal and cardiac muscle disorder presenting with hypertrophic cardiomyopathy, Wolf-Parkinson-White syndrome, skeletal myopathy, and mild intellectual disability. …”
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    Article
  18. 58

    Identification of Signal Pathways and Hub Genes of Pulmonary Arterial Hypertension by Bioinformatic Analysis by Rui-Qi Wei, Wen-Mei Zhang, Zhe Liang, Chunmei Piao, Guangfa Zhu

    Published 2022-01-01
    “…Significant KEGG pathway enrichment included ribosome biogenesis in eukaryotes, RNA transport, proteoglycans in cancer, dilated cardiomyopathy, rheumatoid arthritis, vascular smooth muscle contraction, focal adhesion, regulation of the actin cytoskeleton, and hypertrophic cardiomyopathy. The PPI network identified 10 hub genes including HSP90AA1, CDC5L, MDM2, LRRK2, CFTR, IQGAP1, CAND1, TOP2A, DDX21, and HIF1A. …”
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  19. 59

    Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combi... by Xiang-hong Luo, Rui Zhu, Qian Chen, Pei-hong Shi, Li-sha Na

    Published 2022-01-01
    “…This study aimed to explore the early diagnosis of abnormal left ventricular systolic function of rare pathogenic titin (TTN) mutation gene carriers in familial hypertrophic cardiomyopathy (FHCM) by three-dimensional speckle tracking echocardiography (3D-STE) combined with gene detection. …”
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    Adrenal Insufficiency under Standard Dosage of Glucocorticoid Replacement after Unilateral Adrenalectomy for Cushing’s Syndrome by Kentaro Fujii, Kazutoshi Miyashita, Isao Kurihara, Ken Hiratsuka, Seiji Sato, Kenichi Yokota, Sakiko Kobayashi, Hirotaka Shibata, Hiroshi Itoh

    Published 2016-01-01
    “…The patient was a 62-year-old woman who has had hypertension for 5 years and presented with heart failure due to hypertrophic cardiomyopathy. She consulted with us because of general fatigue, facial edema, and muscle weakness and was diagnosed with Cushing’s syndrome. …”
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