Zobrazeno 1 - 2
of 2
pro vyhledávání: '"J.P. Le Faucheur"'
Autor:
J.P. Le Faucheur, Frédéric Roche, Silvia Oghina, A. Zaroui, V. Plante-Bordeneuve, F. Canoui Poitrine, T. Damy, Arnault Galat, Emmanuel Teiger, S. Guendouz, Mélanie Bézard, S. Silva, Mounira Kharoubi, L. Hittinger, D. Hupin, C. Chalard
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 13:29
Background The prevalence of small-fiber neuropathy (SFN) is high in patients with hereditary transthyretin amyloidosis (ATTRv) but remains unknown in transthyretin wild-type cardiac amyloidosis (ATTRwt-CA). Objective To determine the prevalence of S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5174e464e41974c2d79bf4f6a8d8735e
https://doi.org/10.1016/j.acvdsp.2020.10.096
https://doi.org/10.1016/j.acvdsp.2020.10.096
Autor:
V. Plante, T. Damy, Benoît Funalot, Jean Francois Deux, V. Moulinier Frenkel, Mélanie Bézard, Elsa Poullot, Etienne Audureau, S. Oghina, F. Le Bras, Anissa Moktefi, Arnault Galat, T. Gendre, M. Kharoubi, Emilie Bequignon, J.P. Le Faucheur, L. Hittinger, Vincent Audard, A. Mukedaisi, Pascale Fanen
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 13:30
Aims Cardiac amyloidosis (CA) have a bad prognosis aggravated by diagnostic delay. Cardiologists should be aware that Amyloidosis Extracardiac Disorders (AECD) and cardiac symptoms and history (ACD) may help to improve CA diagnosis and typing. The ai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47340c60d513d65a69e48e701cb9f3d2
https://doi.org/10.1016/j.acvdsp.2020.10.097
https://doi.org/10.1016/j.acvdsp.2020.10.097