Zobrazeno 1 - 10 of 13 pro vyhledávání: '"G.A. Giunta"'
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Radiofrequency ablation of supraventricular arrhythmias after orthotopic heart transplantation: Long-term follow-up of a single-center experience
Autor: N. Galizio, Elian F. Giordanino, Debora A Ramirez, José L. González, Roberto R. Favaloro, María F. Renedo, M. Mysuta, G.A. Giunta, Aldana Ameri, Liliana E. Favaloro, A.M. Bertolotti, D.O. Absi
Publikováno v: Clinical transplantationREFERENCES. 35(2)
Background Supraventricular arrhythmias (SVAs), commonly managed with radiofrequency ablation (RFA), may occur after orthotopic heart transplantation (OHT). Methods We retrospectively assessed 514 consecutive patients (pts.) undergoing OHT between Ja
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a05b4a14044227a5e3fe11ebc730820
https://pubmed.ncbi.nlm.nih.gov/33226674
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3
Short‐term mechanical circulatory support devices as bridge to heart transplantation: A prospective single‐center experience in Argentina
Autor: Aldana Ameri, Daniela M. Rubira, G.A. Giunta, Roberto R. Favaloro, María F. Renedo, R. Ratto, A.M. Bertolotti, D.O. Absi, Elian F. Giordanino, Liliana E. Favaloro
Publikováno v: Clinical Transplantation. 34
Background Patients with cardiogenic shock may require hemodynamic stabilization with short-term mechanical circulatory support devices (ST-MCS) such as extracorporeal membrane oxygenation (ECMO) and centrifugal pump (CP) as bridge to transplantion (
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aeac0147021922da805328cd5d7549b
https://doi.org/10.1111/ctr.13888
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7
Functional analysis of six uncharacterised mutations in LDLR gene
Autor: Ulises Toscanini, Alessandro Pontoglio, María Laura Parolin, Andrea Gomez, L. Helman, G.A. Giunta, Luis Cuniberti, Luciana Kaeser, Roberto Colombo
Publikováno v: Atherosclerosis. 291
Background and aims: Familial hypercholesterolemia (FH) is a primary hyperlipemia. It is an autosomal dominant genetic disorder of lipoproteins metabolism mainly caused by mutations in the low density lipoprotein receptor gene (LDLR). We aimed to inv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0a5224a12bd67f0279447a7e6e782c3
https://pubmed.ncbi.nlm.nih.gov/31689621
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Plný text Recenzováno Digitální knihovna AV ČR
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