Zobrazeno 1 - 10
of 577
pro vyhledávání: '"Attr amyloidosis"'
Autor:
Gabriela Neculae, Robert Adam, Andreea Jercan, Sorina Bădeliță, Catherina Tjahjadi, Mirela Draghici, Claudiu Stan, Jeroen J. Bax, Bogdan A. Popescu, Nina Ajmone Marsan, Daniel Coriu, Ruxandra Jurcuț
Publikováno v:
ESC Heart Failure, Vol 11, Iss 5, Pp 2825-2834 (2024)
Abstract Aims Systemic amyloidosis represents a heterogeneous group of diseases resulting from amyloid fibre deposition. The purpose of this study is to establish a differential diagnosis algorithm targeted towards the two most frequent subtypes of C
Externí odkaz:
https://doaj.org/article/70340846daa34f3497295c6b85d66e68
Autor:
Kon-Ping Lin, Chih-Chao Yang, Yi-Chung Lee, Ming-Jen Lee, John Vest, Marianne T. Sweetser, Matthew T. White, Prajakta Badri, Sung-Tsang Hsieh, Chi-Chao Chao
Publikováno v:
Journal of the Formosan Medical Association, Vol 123, Iss 9, Pp 975-984 (2024)
Background: To examine the efficacy and safety of patisiran, an RNA interference therapeutic, in patients from Taiwan with hereditary transthyretin-mediated (hATTR) amyloidosis with polyneuropathy. Methods: The APOLLO phase 3 trial included patients
Externí odkaz:
https://doaj.org/article/dab5699cac1045209b1a2938728fe680
Publikováno v:
Архивъ внутренней медицины, Vol 14, Iss 4, Pp 312-320 (2024)
The diversity of clinical forms of amyloidosis is related to differences in amyloidogenic precursor proteins. Cardiac involvement is characteristic of AL- and ATTR-amyloidosis, with cardiac involvement developing in the vast majority of patients with
Externí odkaz:
https://doaj.org/article/7a368abea9c741728acb85c84516c51b
Autor:
Xia Wu, Denis Toskic, Ping Zhou, Stephanie Scalia, Xun Ma, Parva Bhatt, Teresa Fogaren, Monika Pilichowska, Knarik Arkun, Jainith Patel, Ron I. Riesenburger, Daniel P. Larson, Raymond L. Comenzo
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 11 (2024)
BackgroundA 63-year-old Black woman presented with progressive exertional dyspnea and chronic lower back pain. The course and findings in her case are instructive.Case reportFamily history was notable for cardiac deaths. An echocardiogram demonstrate
Externí odkaz:
https://doaj.org/article/f5de11a034e6443b91ab3f3ff8f10bdf
Autor:
Nicholas Streicher, Leslie Amass, Rong Wang, Jennifer M. Stephens, Traci LeMasters, Rutika Raina, Emma Merrill, Farooq H. Sheikh
Publikováno v:
Cardiology and Therapy, Vol 13, Iss 2, Pp 359-368 (2024)
Abstract Introduction Transthyretin amyloidosis (ATTR) is a progressive, heterogeneous rare disease manifesting as ATTR polyneuropathy (ATTR-PN), ATTR cardiomyopathy (ATTR-CM), or a mixed phenotype. Tafamidis meglumine (20 mg po qd) is approved in so
Externí odkaz:
https://doaj.org/article/c978271c36ae4ea18deac4030ba008bf
Autor:
Qiuyan Sha, Yanli Zhang, Mengdie Wang, Jialu Sun, Yunlong Zhang, Xinxin Zhang, Ning Wang, Yu Liu, Ying Liu
Publikováno v:
ESC Heart Failure, Vol 11, Iss 1, Pp 112-125 (2024)
Abstract Aims We conducted a presentation on an 84‐year‐old male patient who has been diagnosed with TTRA81V (p. TTRA101V) hereditary transthyretin cardiac amyloidosis (hATTR‐CM). In order to establish its pathogenicity, we extensively investig
Externí odkaz:
https://doaj.org/article/e6ed4631d952469c8912ad10713aba82
Autor:
Steven Lewis, Jingwen Huang, Nidhi Patel, Russell Folks, James Galt, C. David Cooke, Ziduo Zheng, Rebecca Zhang, Ernest Garcia, Jonathon Nye, Marina Piccinelli, Valeria Moncayo, Kunal Bhatt, Adam Mitchell
Publikováno v:
American Heart Journal Plus, Vol 40, Iss , Pp 100377- (2024)
Background: Transthyretin (ATTR) cardiac amyloidosis is associated with an apical-sparing strain pattern on TTE. We hypothesize that strain indices derived from myocardial perfusion imaging (MPI) can identify this abnormality. Methods: A group with A
Externí odkaz:
https://doaj.org/article/f60e6881e5384311be2b143a752b659f
Autor:
Yukio Ando, Marcia Waddington-Cruz, Yoshiki Sekijima, Haruki Koike, Mitsuharu Ueda, Hiroaki Konishi, Tomonori Ishii, Teresa Coelho
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-17 (2023)
Abstract Hereditary transthyretin (ATTRv) amyloidosis is a rare and autosomal dominant disorder associated with mutations in the transthyretin gene. Patients present with diverse symptoms related to sensory, motor, and autonomic neuropathy, as well a
Externí odkaz:
https://doaj.org/article/b4211bad5c5b4a2f92847c0a1e464bdc
Autor:
Gnana Deepthi Medarametla, Ripudaman Singh Kahlon, Lampimukhi Mahitha, Sanobar Shariff, Naga Praneeth Vakkalagadda, Hitesh Chopra, Mohammad Amjad Kamal, Neil Patel, Yashendra Sethi, Nirja Kaka
Publikováno v:
EXCLI Journal : Experimental and Clinical Sciences, Vol 22, Pp 781-808 (2023)
Amyloidosis is a protein deposition disorder in which insoluble fibril structures accumulate in the bodily tissues damaging the organ function. Cardiac amyloidosis is a severe but under-reported medical condition characterized by the accumulation of
Externí odkaz:
https://doaj.org/article/1bdec78d7f2f4ffd8a9c01fe3a5865ff
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.