Introduction: Systemic amyloidosis is a condition where amyloid proteins accumulate in organs and tissues, causing multisystem dysfunction. Its presentation often overlaps with other conditions like lymphoproliferative disorders and multiple myeloma (MM).
Naciye Nur Tozluklu+3 more
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Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis
Daniel R. Jacobson+2 more
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Treatment options for severe cardiac amyloidosis: heart transplantation combined with chemotherapy and stem cell transplantation for patients with AL-amyloidosis and heart and liver transplantation for patients with ATTR-amyloidosis☆ [PDF]
Falk‐Udo Sack+6 more
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Tumor thrombus is a very rare complication observed in patients with hepatocellular carcinoma. We report a unique case of hepatocellular carcinoma with extension of tumor along the inferior vein cava into the right atrium, in a patient with cardiac ...
Valeria Mancusi, MD+3 more
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Intraoperative Death in Cardiac Amyloidosis with Increased QT Dispersion in the Electrocardiogram
Minna Tallgren+4 more
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Cardiac amyloidosis: MR imaging findings and T1 quantification, comparison with control subjects [PDF]
Gabriele A. Krombach+6 more
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Hypertrophic Cardiomyopathy Complicated with Cardiac Amyloidosis.
Isao Kohno+8 more
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Cardiovascular Magnetic Resonance and prognosis in cardiac amyloidosis [PDF]
Alicia M. Maceira+4 more
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Autologous PBSCT in patients with cardiac amyloidosis
JM Stevens+7 more
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223 Adverse functional significance of delayed enhancement on cardiac MRI in primary systemic amyloidosis [PDF]
Raymond Q. Migrino+5 more
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