Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Arnault, Galat"'
Autor:
Antoine Fraix, Emmanuel Itti, Amira Zaroui, Mounira Kharoubi, Elsa Poullot, Lionel Lerman, Soulef Guendouz, Olivier Huttin, Thibaud Damy, Arnault Galat
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Bone scintigraphy (BS) is established as an accurate, non-invasive method for the diagnosis of transthyretin amyloid cardiomyopathy (ATTR-CM). In a real-life setting, however, some patients with no cardiac uptake on BS turn out to
Externí odkaz:
https://doaj.org/article/bf1ca15f925e4624bc95c4b70eed9662
Prognostic mortality factors in advanced light chain cardiac amyloidosis: A prospective cohort study
Autor:
Amira Zaroui, Mounira Kharoubi, Romain Gounot, Silvia Oghina, Charlotte Degoutte, Melanie Bezard, Arnault Galat, Soulef Guendouz, Louise Roulin, Vincent Audard, Vincent Leroy, Emmanuel Teiger, Elsa Poullot, Valérie Molinier‐Frenkel, Fabien Le Bras, Karim Belhadj, Jean‐Philippe Bastard, Soraya Fellahi, Jason Shourick, Francois Lemonier, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 11, Iss 3, Pp 1707-1719 (2024)
Abstract Aims Predicting mortality in severe AL cardiac amyloidosis is challenging due to elevated biomarker levels and limited thresholds for stratifying severe cardiac damage. Methods and results This prospective, observational, cohort study includ
Externí odkaz:
https://doaj.org/article/4489b3e559bd42f39fe6942bd5d6b2af
Autor:
Mohamed‐Salah Annabi, Rasmus Carter‐Storch, Amira Zaroui, Arnault Galat, Silvia Oghina, Mounira Kharoubi, Mélanie Bezard, Geneviève Derumeaux, Pascale Fanen, François Lemonnier, Elsa Poullot, Emmanuel Itti, Romain Gallet, Emmanuel Teiger, Philippe Pibarot, Thibaud Damy, Marie‐Annick Clavel
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 13, Iss 13 (2024)
Background Cardiac amyloidosis (CA) is frequently found in older patients with aortic stenosis (AS). However, the prevalence of AS among patients with CA is unknown. The objective was to study the prevalence and prognostic impact of AS among patients
Externí odkaz:
https://doaj.org/article/336167ce5599455cbaa367e7c56c2ad4
Autor:
Mounira Kharoubi, Mélanie Bézard, Amaury Broussier, Arnault Galat, Romain Gounot, Elsa Poullot, Valérie Molinier-Frenkel, Pascale Fanen, Benoit Funalot, Emmanuel Itti, François Lemonnier, Gagan Deep Sing Chadha, Soulef Guendouz, Sophie Mallet, Amira Zaroui, Vincent Audard, Etienne Audureau, Philippe Le Corvoisier, Luc Hittinger, Violaine Planté Bordeneuve, Jean-Pascal Lefaucheur, Aurélien Amiot, Emilie Bequignon, Sophie Bartier, Vincent Leroy, Emmanuel Teiger, Silvia Oghina, Thibaud Damy
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
Background and aimsSelf-reported questionnaires are useful for estimating the health-related quality of life (HR-QoL), impact of interventions, and prognosis. To our knowledge, no HR-QoL questionnaire has been developed for cardiac amyloidosis (CA).
Externí odkaz:
https://doaj.org/article/dcf4c81b00fa4118afed6e4bc8292064
Autor:
Antoine Jobbé‐Duval, Mélanie Bézard, Stéphane Moutereau, Mounira Kharoubi, Silvia Oghina, Amira Zaroui, Arnault Galat, Coraline Chalard, Elisabeth Hugon‐Vallet, Francois Lemonnier, Damien Eyharts, Elsa Poulot, Pascale Fanen, Benoit Funalot, Valérie Molinier‐Frenkel, Vincent Audard, Luc Hittinger, Marc Antoine Delbarre, Emmanuel Teiger, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 9, Iss 2, Pp 1314-1327 (2022)
Abstract Aims Iron deficiency (ID) is common in patient with chronic heart failure (HF) and has been widely studied. In contrast, data concerning ID in cardiac amyloidosis (CA) are limited. Amyloidosis is a severe and fatal systemic disease, characte
Externí odkaz:
https://doaj.org/article/1655f7014e624439b01d1f60dddf39e8
Autor:
Mounira Kharoubi, Mélanie Bézard, Arnault Galat, Fabien Le Bras, Elsa Poullot, Valérie Molinier‐Frenkel, Pascale Fanen, Benoit Funalot, Anissa Moktefi, Jean‐Pascal Lefaucheur, Mukedaisi Abulizi, Jean‐François Deux, François Lemonnier, Soulef Guendouz, Coraline Chalard, Amira Zaroui, Vincent Audard, Emilie Bequignon, Diane Bodez, Emmanuel Itti, Luc Hittinger, Etienne Audureau, Emmanuel Teiger, Silvia Oghina, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 8, Iss 6, Pp 5501-5512 (2021)
Abstract Aims Cardiac amyloidosis (CA) has a poor prognosis which is aggravated by diagnostic delay. Amyloidosis extracardiac and cardiac events (AECE and ACE) may help improve CA diagnosis and typing. The aim of this study was to compare AECE and AC
Externí odkaz:
https://doaj.org/article/3f9995dbd45047888c9a849396bbdb31
Autor:
Mounira Kharoubi, Fréderic Roche, Mélanie Bézard, David Hupin, Sidney Silva, Silvia Oghina, Coraline Chalard, Amira Zaroui, Arnault Galat, Soulef Guendouz, Florence Canoui‐Poitrine, Luc Hittinger, Emmanuel Teiger, Jean‐Pascal Lefaucheur, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 8, Iss 2, Pp 1656-1665 (2021)
Abstract Aims The prevalence of autonomic neuropathy (AN) is high in patients with hereditary transthyretin amyloidosis but remains unknown in transthyretin wild‐type cardiac amyloidosis (ATTRwt‐CA). This study aimed to determine the prevalence o
Externí odkaz:
https://doaj.org/article/862ef009bb0841f690fee97761607e82
Autor:
Arnault Galat, Aziz Guellich, Diane Bodez, Larissa Lipskaia, Stéphane Moutereau, Eric Bergoend, Sophie Hüe, Julien Ternacle, Dania Mohty, Jean‐Luc Monin, Geneviève Derumeaux, Costin Radu, Thibaud Damy
Publikováno v:
ESC Heart Failure, Vol 6, Iss 4, Pp 649-657 (2019)
Abstract Aims Cardiac fibrosis is associated with left ventricular (LV) remodelling and contractile dysfunction in aortic stenosis (AS). The fibrotic process in this condition is still unclear. The aim of this study was to determine the role of both
Externí odkaz:
https://doaj.org/article/722f973c96654411ad512a702da31516
Autor:
Mélanie Bézard, Silvia Oghina, Damien Vitiello, Mounira Kharoubi, Ekaterini Kordeli, Arnault Galat, Amira Zaroui, Soulef Guendouz, Floriane Gilles, Jason Shourick, David Hamon, Vincent Audard, Emmanuel Teiger, Elsa Poullot, Valérie Molinier-Frenkel, François Lemonnier, Onnik Agbulut, Fabien Le Bras, Thibaud Damy
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0257189 (2021)
BackgroundCardiac light chain amyloidosis (AL-CA) patients often die within three months of starting chemotherapy. Chemotherapy for non-immunoglobulin M gammopathy with AL-CA frequently includes bortezomib (Bor), cyclophosphamide (Cy), and dexamethas
Externí odkaz:
https://doaj.org/article/bbbf2a9e4d304b4583602af0c7c9d90b
Autor:
Shirley Odouard, Mukedaisi Abulizi, Mounira Kharoubi, Silvia Oghina, Soulef Guendouz, Amira Zaroui, Emmanuel Teiger, Emmanuel Itti, Thibaud Damy, Arnault Galat
Publikováno v:
JACC: Cardiovascular Imaging. 15:2149-2151