Kon-Ping Lin
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Explore the profile of Kon-Ping Lin including associated specialties, affiliations and a list of published articles.
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78
Citations
1833
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Recent Articles
1.
Hung Y, Yu A, Chen Y, Tsai C, Su M, Shun C, et al.
J Formos Med Assoc
. 2024 Oct;
PMID: 39389803
Background: RNA interference therapeutics reduce transthyretin production; however, their effect on hereditary transthyretin amyloid cardiomyopathy (ATTR-CA) remains unclear. We aimed to investigate alterations in technetium-99 m (Tc)-pyrophosphate (PYP) single-photon emission...
2.
Lin K, Yang C, Lee Y, Lee M, Vest J, Sweetser M, et al.
J Formos Med Assoc
. 2024 Mar;
123(9):975-984.
PMID: 38548524
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...
3.
Obici L, Ajroud-Driss S, Lin K, Berk J, Gillmore J, Kale P, et al.
Neurol Ther
. 2023 Jul;
12(5):1759-1775.
PMID: 37523143
Introduction: Hereditary transthyretin (ATTRv; v for variant) amyloidosis, also known as hATTR amyloidosis, is a progressive and fatal disease associated with rapid deterioration of physical function and patients' quality of...
4.
Jih K, Lai K, Lin K, Liao Y, Lee Y
J Chin Med Assoc
. 2023 Jan;
86(1):47-51.
PMID: 36599142
Background: Expanded HTT alleles with 40 or more CAG repeats were recently found to be a rare cause of frontotemporal dementia and amyotrophic lateral sclerosis (ALS) spectrum diseases. The aim...
5.
Hsu S, Liao Y, Lin K, Lin P, Yu K, Tsai Y, et al.
Parkinsonism Relat Disord
. 2022 Sep;
103:144-149.
PMID: 36155026
Background: Hereditary spastic paraplegia (HSP) is a heterogeneous group of inherited neurodegenerative disorders characterized by slowly progressive lower limbs spasticity and weakness. HSP type 30 (SPG30) is a HSP subtype...
6.
Chao H, Hsiao C, Lai K, Tsai Y, Lin K, Liao Y, et al.
J Formos Med Assoc
. 2022 Aug;
122(2):132-138.
PMID: 36031490
Background: Mutations in the neurofilament light polypeptide gene (NEFL) are an uncommon cause of Charcot-Marie-Tooth disease (CMT). The aim of this study is to elucidate the clinical characteristics and genetic...
7.
Hsu S, Jih K, Lin K, Liao Y, Lee Y
Parkinsonism Relat Disord
. 2022 Feb;
96:43-44.
PMID: 35180462
We investigated 98 Taiwanese patients with molecularly unassigned hereditary spastic paraplegia (HSP) and found none of them had the NOTCH2NLC GGC repeat expansion, which is the cause of neuronal intranuclear...
8.
Liu Y, Guo Y, Lin L, Tsai C, Fuh J, Wang Y, et al.
J Formos Med Assoc
. 2021 Nov;
121(9):1647-1656.
PMID: 34802834
Background/purpose: The long-term disease course and efficacy of maintenance therapies have rarely been investigated in Asian patients with neuromyelitis optica spectrum disorder (NMOSD). Methods: Medical records of patients fulfilling the...
9.
Tsai P, Jih K, Shen T, Liu Y, Lin K, Liao Y, et al.
Neurol Genet
. 2021 Nov;
7(6):e627.
PMID: 34746377
Background And Objectives: To investigate the frequency, spectrum, and molecular functional effect of glycosyltransferase 8 domain-containing protein 1 (GLT8D1) variations in Taiwanese patients with amyotrophic lateral sclerosis (ALS). Methods: We...
10.
Liao Y, Chang F, Huang H, Chen T, Chou Y, Hsu S, et al.
Neurology
. 2021 Oct;
98(2):e199-e206.
PMID: 34675106
Background And Objectives: The GGC repeat expansion in the 5' untranslated region of was recently identified as the cause of neuronal intranuclear inclusion disease (NIID), which may manifest with peripheral...