Huirong Peng
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Explore the profile of Huirong Peng including associated specialties, affiliations and a list of published articles.
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39
Citations
306
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Recent Articles
1.
Chen X, Peng H, Sun X, Yan L, Feng X, Fan S, et al.
Small
. 2025 Mar;
:e2500710.
PMID: 40042409
Cesium lead iodide (CsPbI₃) is a promising material for semitransparent perovskite solar cells (ST-PSCs) in building-integrated photovoltaics (BIPV) due to its favorable bandgap and thermal stability. However, the phase instability...
2.
Lei L, Peng L, Wan L, Chen Z, Wang C, Peng H, et al.
Mov Disord
. 2024 Dec;
40(2):324-334.
PMID: 39699045
Background: Recent studies have reported that expanded GCA repeats in the GLS gene can cause glutaminase deficiency with ataxia phenotype. However, to data, no studies have investigated the distribution and...
3.
Ouyang R, Wan L, Pellerin D, Long Z, Hu J, Jiang Q, et al.
EBioMedicine
. 2024 Mar;
102:105077.
PMID: 38513302
Background: An intronic GAA repeat expansion in FGF14 was recently identified as a cause of GAA-FGF14 ataxia. We aimed to characterise the frequency and phenotypic profile of GAA-FGF14 ataxia in...
4.
Shi Y, Zou G, Chen Z, Wan L, Peng L, Peng H, et al.
J Neurol
. 2023 Jul;
270(11):5372-5379.
PMID: 37433893
Background: Spinocerebellar ataxia type 3 (SCA3) is the most common subtype of SCA without effective treatment. This study aimed to evaluate the comparative efficacy of low-frequency repetitive transcranial magnetic stimulation...
5.
Peng L, Wan L, Liu M, Long Z, Chen D, Yuan X, et al.
J Neurol
. 2023 May;
270(9):4248-4261.
PMID: 37184660
Background: The longitudinal dynamics of neurofilament light chain (NfL) in multiple system atrophy (MSA) were incompletely illuminated. This study aimed to explore whether the plasma NfL (pNfL) could serve as...
6.
Chen Z, Liao G, Wan N, He Z, Chen D, Tang Z, et al.
Mov Disord
. 2023 Apr;
38(6):978-989.
PMID: 37023261
Background: Severe reduced synaptic density was observed in spinocerebellar ataxia (SCA) in postmortem neuropathology, but in vivo assessment of synaptic loss remains challenging. OBJECTIVE SPINOCEREBELLAR ATAXIA TYPE 3: The objective...
7.
Shi Y, Peng L, Zou G, Chen Z, Wan L, Tang Z, et al.
Parkinsonism Relat Disord
. 2022 Oct;
104:58-63.
PMID: 36244162
Introduction: Spinocerebellar ataxia type 3 (SCA3) is the most common subtype of hereditary ataxia. Few studies reported the CMCT features in SCA3, but with inconsistent findings. So far, CMCT in...
8.
Shi Y, Fu Y, Tao Z, Yong W, Peng H, Jian W, et al.
Genes Genomics
. 2022 Aug;
45(3):359-365.
PMID: 35951155
Background: Walker-Warburg syndrome (WWS) is a genetically heterogeneous disease that often presents with complex brain and eye malformations and congenital muscular dystrophy. Mutations of the ISPD gene have been identified...
9.
Peng Y, Peng L, Chen Z, Peng H, Wang P, Zhang Y, et al.
Front Aging Neurosci
. 2022 Jul;
14:917126.
PMID: 35865750
Objective: The natural history of spinocerebellar ataxia type 3 (SCA3) has been reported in several populations and shows heterogeneity in progression rate and affecting factors. However, it remains unexplored in...
10.
Peng L, Peng Y, Chen Z, Wang C, Long Z, Peng H, et al.
J Transl Med
. 2022 May;
20(1):226.
PMID: 35568848
Background: In polyglutamine (polyQ) diseases, the identification of modifiers and the construction of prediction model for progression facilitate genetic counseling, clinical management and therapeutic interventions. Methods: Data were derived from...