致敬
发表于 2025-3-26 20:57:26
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Atmosphere
发表于 2025-3-27 02:22:39
Kyle James Downey,Margaret Rush Drekerhere have not yet been any prospective randomized therapeutic studies with precisely characterized patient populations. Ultimately decisive for the development of adequate therapeutic strategies, however, is a precise clinical evaluation of the patients to be treated. Besides documenting the clinica
concubine
发表于 2025-3-27 05:55:06
https://doi.org/10.1007/978-88-470-2155-6Dilated cardiomyopathy; circulation; familial cardiomyopathies; genetics; heart; heart transplantation; hy
Macronutrients
发表于 2025-3-27 11:25:59
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MERIT
发表于 2025-3-27 14:21:54
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混合
发表于 2025-3-27 20:07:51
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冷漠
发表于 2025-3-28 00:00:09
Scripting, AI, and Depth (and Death),The morphological, functional, and genetic abnormalities are heterogeneous in different patient populations with hypertrophie cardiomyopathy (HCM) ; as a consequence, the natural history and the clinical course are extremely variable and prognostic evaluation is a challenging task in the individual patient.
丛林
发表于 2025-3-28 05:49:50
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molest
发表于 2025-3-28 08:28:45
Overview: 978-88-470-2181-5978-88-470-2155-6
柱廊
发表于 2025-3-28 12:37:30
https://doi.org/10.1007/978-1-4302-0980-5asymptomatic course to severe heart failure and cardiac arrest. Ventricular arrhythmias, palpitations and syncope are frequent signs and symptoms. Sudden, unexpected cardiac arrest is a pending catastrophe in the natural history of HCM.