Hereditary and wild type transthyretin amyloid cardiomyopathy in Bulgaria in patients suspected for cardiac amyloidosis

Introduction: Transthyretin amyloid cardiomyopathy (ATTR-CM) is a severe progressive disease, more common than previously expected. The main objectives were to evaluate hereditary and wild type ATTR-CM frequency and clinical manifestations. Material and methods: One hundred seventy-eight patients at...

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Váldodahkkit:	S. Stefanov, N. Stoyanov, N. Koleva, D. Mikova, A. Yordanov, Z. Pavlova, E. Kinova, I. Petrova, L. Demirevska, T. Todorov, T. Chamova, M. Garcheva, A. Kundurdjiev, A. Todorova, I. Tournev, Y. Palashev, I. Daskalov, M. Dimova, I. Gruev, Y. Yotov, A. Goudev, V. Velchev, Mariana Gospodinova
Materiálatiipa:	Artigo
Giella:	Búlgaro
Almmustuhtton:	Pensoft Publishers 2024-09-01
Ráidu:	Българска кардиология
Fáttát:	amyloidosis transthyretin cardiomyopathy red fla
Liŋkkat:	https://journal.bgcardio.org/article/127340/download/pdf/
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