Sung-Tsang Hsieh
Overview
Explore the profile of Sung-Tsang Hsieh including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
165
Citations
1958
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
21.
Yeh S, Yeh T, Wang Y, Chao C, Tzeng S, Tang T, et al.
Ann Clin Transl Neurol
. 2023 Oct;
11(1):30-44.
PMID: 37902278
Objective: Despite amyloid deposition as a hallmark of hereditary transthyretin amyloidosis (ATTRv) with polyneuropathy, this pathology could not completely account for nerve degeneration. ATTRv patients frequently have vasomotor symptoms, but...
22.
Tsai C, Chao C, Hsieh S, Yu A, Wu Y, Cheng M, et al.
Orphanet J Rare Dis
. 2023 Sep;
18(1):289.
PMID: 37705003
Background: Transthyretin cardiac cardiomyopathy (ATTR-CM) is a rare but life-threatening disease. Tafamidis is an effective treatment for patients with ATTR-CM, however its long-term effects on cardiac remodeling and cardiac amyloid...
23.
24.
Yeh T, Chang M, Kan Y, Chiang H, Hsieh S
Mol Neurobiol
. 2023 Sep;
61(2):707-724.
PMID: 37656312
The role of heat shock protein 27 (HSP27), a chaperone, in neuropathic pain after nerve injury has not been systematically surveyed despite its neuroprotective and regeneration-promoting effects. In this study,...
25.
Tsai C, Yu A, Wu Y, Su M, Cheng M, Chou C, et al.
Acta Cardiol Sin
. 2023 Jul;
39(4):619-627.
PMID: 37456942
Background: Hereditary transthyretin amyloid cardiomyopathy (ATTR-CM) is a progressive and fatal disease. A97S (p.Ala117Ser) is the most common transthyretin genetic mutation in Taiwan. Tafamidis is a transthyretin stabilizer, and it...
26.
Hsueh H, Kao H, Chao C, Hsueh S, Huang Y, Lin W, et al.
Neurol Genet
. 2023 Jun;
9(4):e200078.
PMID: 37346931
Background And Objectives: Charcot-Marie-Tooth disease (CMT) is a syndrome of a hereditary neurodegenerative condition affecting the peripheral nervous system and is a single gene disorder. Deep phenotyping coupled with advanced...
27.
Hsueh S, Chao C, Chen T, Chen Y, Hsueh H, Tsai L, et al.
Ann Clin Transl Neurol
. 2023 Jun;
10(8):1456-1466.
PMID: 37340732
Objective: This study aimed to explore the clinical significance of brain imaging signatures in the context of clinical neurological deficits in association with upper and lower motor neuron degeneration in...
28.
Chen S, Lien P, Lin F, Chou P, Chen C, Chen Z, et al.
Int J Biol Macromol
. 2023 Apr;
241:124636.
PMID: 37119896
Peripheral nerve injuries are commonly encountered in extremity traumas. Their motor and sensory recovery following microsurgical repair is limited by slow regeneration speed (<1 mm/d) and subsequent muscle atrophy, which...
29.
Chen P, Chao C, Tsai L, Huang H, Chien Y, Huang P, et al.
J Neuromuscul Dis
. 2023 Apr;
10(4):667-684.
PMID: 37066920
Background: Whole-exome sequencing (WES) facilitates the diagnosis of hereditary neuromuscular disorders. To achieve an accurate diagnosis, physicians should interpret the genetic report carefully along with clinical information and examinations. We...
30.
Chang H, Yeh S, Chiang M, Hsieh S
BMC Med Imaging
. 2023 Mar;
23(1):44.
PMID: 36973775
Background: Experimental ischemic stroke models play a fundamental role in interpreting the mechanism of cerebral ischemia and appraising the development of pathological extent. An accurate and automatic skull stripping tool...