Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Yuanfeng Miao"'
Autor:
Kang Du, Fan Li, Hui Wang, Yuanfeng Miao, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Lingchao Meng
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 8, Iss 4, Pp 831-841 (2021)
Abstract Objective This study aims to report the genotypes and phenotypes of hereditary transthyretin amyloidosis (ATTR) in a large Chinese cohort, yet the clinical and genetic profiles of ATTR remain elusive in mainland China. Methods Fifty‐four p
Externí odkaz:
https://doaj.org/article/b0f2c785bb0e4ea99bcd43b2a6fec02e
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: There are few reported cases of posterior reversible encephalopathy syndrome (PRES) combined with essential thrombocythemia (ET). We report a case of PRES-like syndrome in ET.Case Report: A 60-year-old man with a history of hypertension a
Externí odkaz:
https://doaj.org/article/fb6dfc10af624639bc30a5146bf0caea
Publikováno v:
Clinical Neuropathology. 40:328-332
Objective Pleckstrin homology domain-containing family G member 5 (PLEKHG5) is a nuclear factor-κ-B-activator gene that predominantly expresses in the neurons and Schwann cells of the peripheral nervous system. Variations in the PLEKHG5 have shown a
Autor:
Wei Zhang, Lingchao Meng, He Lv, Yun Yuan, Hui Wang, Zhaoxia Wang, Yuanfeng Miao, Kang Du, Fan Li
Publikováno v:
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 8, Iss 4, Pp 831-841 (2021)
Annals of Clinical and Translational Neurology, Vol 8, Iss 4, Pp 831-841 (2021)
Objective This study aims to report the genotypes and phenotypes of hereditary transthyretin amyloidosis (ATTR) in a large Chinese cohort, yet the clinical and genetic profiles of ATTR remain elusive in mainland China. Methods Fifty‐four patients w