Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Weng Tein Gi"'
Autor:
Arjan Sammani, Elham Kayvanpour, Laurens P. Bosman, Farbod Sedaghat‐Hamedani, Tanja Proctor, Weng‐Tein Gi, Alicia Broezel, Katrin Jensen, Hugo A. Katus, Anneline S.J.M. teRiele, Benjamin Meder, Folkert W. Asselbergs
Publikováno v:
ESC Heart Failure, Vol 7, Iss 4, Pp 1430-1441 (2020)
Abstract Aims Patients with non‐ischaemic dilated cardiomyopathy (DCM) are at increased risk of sudden cardiac death. Identification of patients that may benefit from implantable cardioverter‐defibrillator implantation remains challenging. In thi
Externí odkaz:
https://doaj.org/article/cc41030b9e674dd78e693b71ca92b738
Autor:
Farbod Sedaghat‐Hamedani, Elham Kayvanpour, Sonja Hamed, Lutz Frankenstein, Johannes Riffel, Weng‐Tein Gi, Ali Amr, Omid Shirvani Samani, Jan Haas, Tobias Miersch, Esther Herpel, Michael M. Kreusser, Philipp Ehlermann, Hugo A. Katus, Benjamin Meder
Publikováno v:
ESC Heart Failure, Vol 7, Iss 2, Pp 692-696 (2020)
Abstract Cardiac sarcoidosis is a chronic inflammatory disease with a large spectrum of symptoms that can mimic diseases such as dilated, hypertrophic, or arrhythmogenic cardiomyopathies. It can be asymptomatic but can also present with ventricular a
Externí odkaz:
https://doaj.org/article/afba56e4ea7548a8a0b925d681252083
Autor:
Weng-Tein Gi, MD, MSc, Farbod Sedaghat-Hamedani, MD, Omid Shirvani Samani, MD, Elham Kayvanpour, MD, Esther Herpel, MD, Rawa Arif, MD, Johannes Riffel, MD, Derliz Mereles, MD, Hugo A. Katus, MD, Benjamin Meder, MD
Publikováno v:
JACC: Case Reports, Vol 2, Iss 3, Pp 378-383 (2020)
We report a rare case of concomitant hypertrophic cardiomyopathy and cardiac myxoma without LEOPARD syndrome. Additionally, 6 similar cases were systemically reviewed, and the characteristics of this first-ever studied patient group were summarized.
Externí odkaz:
https://doaj.org/article/8f6200146a8541e5a842c9189bea39f3
Autor:
Weng-Tein Gi, MD, MSc, Ali Amr, MD, Farbod Sedaghat-Hamedani, MD, Elham Kayvanpour, MD, Isabell Mohr, BSc, Manuela Meder, MD, Omid Shirvani Samani, MD, Herbert Fluhr, MD, Hugo A. Katus, MD, Benjamin Meder, MD
Publikováno v:
JACC: Case Reports, Vol 2, Iss 1, Pp 139-144 (2020)
Hypertrophic obstructive cardiomyopathy (HOCM) increases the risk for mother and fetus during pregnancy. Alcohol septal ablation (ASA) is an established procedure in nonpregnant patients with HOCM. In this report, we present a case of a 29-year-old w
Externí odkaz:
https://doaj.org/article/3f9f1593870845f2ae91f830bb02d54f
Autor:
Philippe Charron, Benjamin Meder, Jan Haas, Grażyna Truszkowska, Mateusz Śpiewak, Hugo A. Katus, Pierre Socie, Eric Villard, Pascale Richard, Jan Koelemenoglu, Małgorzata Stępień-Wojno, Farbod Sedaghat-Hamedani, Bogna Foss-Nieradko, Weng-Tein Gi, Joanna Zakrzewska-Koperska, Elham Kayvanpour, Arjan Sammani, Ewa Michalak, Anneline S.J.M. te Riele, Folkert W. Asselbergs, Tobias Miersch, Tomasz Zieliński, Zofia T. Bilińska, Norbert Frey, Annette F. Baas, Alicia Broezel, Przemysław Chmielewski, Angelique Curjol, Rafał Płoski, David H. Lehmann
Publikováno v:
International journal of cardiology, 339, 75-82. Elsevier Ireland Ltd
Background Non-ischemic dilated cardiomyopathy (DCM) can be complicated by sustained ventricular arrhythmias (SVA) and sudden cardiac death (SCD). By now, left-ventricular ejection fraction (LV-EF) is the main guideline criterion for primary prophyla
Autor:
Tanja Proctor, Arjan Sammani, Hugo A. Katus, Weng-Tein Gi, Laurens P Bosman, Farbod Sedaghat-Hamedani, Benjamin Meder, Alicia Broezel, Folkert W. Asselbergs, Anneline S.J.M. te Riele, Katrin Jensen, Elham Kayvanpour
Publikováno v:
ESC Heart Failure, Vol 7, Iss 4, Pp 1430-1441 (2020)
Aims Patients with non‐ischaemic dilated cardiomyopathy (DCM) are at increased risk of sudden cardiac death. Identification of patients that may benefit from implantable cardioverter‐defibrillator implantation remains challenging. In this study,
Autor:
Sih-Shiang Huang, Chien-Chang Lee, Gin Hoong Lee, Evangelos Giannitsis, Weng-Tein Gi, Cho-Hung Chiang, Yuan-Kun Wu, Cho-Han Chiang, Yee Hui Yeo
Publikováno v:
Heart. 106:985-991
ObjectiveThe European Society of Cardiology (ESC) 0/1 hour algorithm has been primarily validated in Europe, America and Australasia with less knowledge of its performance outside of these settings. We aim to evaluate the performance of the ESC 0/1 h
Autor:
Omid Shirvani Samani, Hugo A. Katus, Benjamin Meder, Esther Herpel, Johannes Riffel, Farbod Sedaghat-Hamedani, Weng-Tein Gi, Rawa Arif, Derliz Mereles, Elham Kayvanpour
Publikováno v:
JACC: Case Reports, Vol 2, Iss 3, Pp 378-383 (2020)
JACC Case Reports
JACC Case Reports
We report a rare case of concomitant hypertrophic cardiomyopathy and cardiac myxoma without LEOPARD syndrome. Additionally, 6 similar cases were systemically reviewed, and the characteristics of this first-ever studied patient group were summarized.
Autor:
Benjamin Meder, Herbert Fluhr, Isabell Mohr, Omid Shirvani Samani, Ali Amr, Elham Kayvanpour, Farbod Sedaghat-Hamedani, Hugo A. Katus, Manuela Meder, Weng-Tein Gi
Publikováno v:
JACC Case Reports
JACC: Case Reports, Vol 2, Iss 1, Pp 139-144 (2020)
JACC: Case Reports, Vol 2, Iss 1, Pp 139-144 (2020)
Hypertrophic obstructive cardiomyopathy (HOCM) increases the risk for mother and fetus during pregnancy. Alcohol septal ablation (ASA) is an established procedure in nonpregnant patients with HOCM. In this report, we present a case of a 29-year-old w
Autor:
Ali Amr, Weng-Tein Gi, Sonja Hamed, Elham Kayvanpour, Omid Shirvani Samani, Jan Haas, Philipp Ehlermann, Benjamin Meder, Farbod Sedaghat-Hamedani, Esther Herpel, Johannes Riffel, Tobias Miersch, Hugo A. Katus, Lutz Frankenstein, Michael M. Kreusser
Publikováno v:
ESC Heart Failure
ESC Heart Failure, Vol 7, Iss 2, Pp 692-696 (2020)
ESC Heart Failure, Vol 7, Iss 2, Pp 692-696 (2020)
Cardiac sarcoidosis is a chronic inflammatory disease with a large spectrum of symptoms that can mimic diseases such as dilated, hypertrophic, or arrhythmogenic cardiomyopathies. It can be asymptomatic but can also present with ventricular arrhythmia