Cargando…
Phenotypic expressions of hereditary Transthyretin Ala97Ser related Amyloidosis (ATTR) in Taiwanese
BACKGROUND: The disease course and early signs specific to ATTR Ala97Ser, the most common endemic mutation in Taiwan, have not been well described. Since new medications can slow down the rate of disease progression, the early diagnosis of this heterogeneous and fatal disease becomes critical. METHO...
Autores principales: | Hsu, Hui-Ching, Liao, Ming-Feng, Hsu, Jung-Lung, Lo, Ai-Lun, Kuo, Hung-Chou, Lyu, Rong-Kuo, Wu, Victor Chien-Chia, Wang, Chih-Wei, Ro, Long-Sun |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5590125/ https://www.ncbi.nlm.nih.gov/pubmed/28882124 http://dx.doi.org/10.1186/s12883-017-0957-4 |
Ejemplares similares
-
Biophysical characterization and modulation of Transthyretin Ala97Ser
por: Liu, Yo‐Tsen, et al.
Publicado: (2019) -
Tafamidis for autonomic neuropathy in hereditary transthyretin (ATTR) amyloidosis: a review
por: Cruz, Márcia Waddington
Publicado: (2019) -
Ala97Ser transthyretin amyloidosis-associated polyneuropathy, clinical and neurophysiological profiles in a Thai cohort
por: Pasutharnchat, Nath, et al.
Publicado: (2021) -
Tafamidis decreased cardiac amyloidosis deposition in patients with Ala97Ser hereditary transthyretin cardiomyopathy: a 12-month follow-up cohort study
por: Tsai, Cheng-Hsuan, et al.
Publicado: (2023) -
Common transthyretin-derived amyloid fibril structures in patients with hereditary ATTR amyloidosis
por: Steinebrei, Maximilian, et al.
Publicado: (2023)