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Yufen Peng

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Articles 11
Citations 42
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Recent Articles
1.
Peng Y, Long Y, Wan C
J Neuropathol Exp Neurol . 2024 Dec; 84(3):223-235. PMID: 39707156
Ischemic strokes pose serious risks to human health. We aimed to elucidate the function of NOD-like receptor X1 (NLRX1) in a rat middle cerebral artery occlusion (MCAO)-induced cerebral ischemia/reperfusion injury...
2.
Long Y, Peng Y, Huang Z, Zhu M, Wan C
Cytojournal . 2024 Aug; 21:24. PMID: 39108465
Objective: The objective of this study was to investigate the cytological features and diagnostic significance of cerebrospinal fluid (CSF) in bacterial meningitis (BM). Material And Methods: Patients diagnosed with BM...
3.
Peng Y, Tu Q, Han Y, Gao L, Wan C
Open Life Sci . 2023 Dec; 18(1):20220762. PMID: 38152578
Neurologists have a difficult time identifying sporadic cerebellar ataxia. Multiple system atrophy of the cerebellar type (MSA-C), spontaneous late cortical cerebellar atrophy, and prolonged alcohol use are a few possible...
4.
Cai S, Huang F, Wang R, Wu M, Liu M, Peng Y, et al.
Front Cardiovasc Med . 2023 Jun; 10:1174466. PMID: 37378408
Purpose: This study evaluates the association between habitual physical activity (HPA) and the outcomes of patients with myocardial infarction (MI). Methods: Patients newly diagnosed with MI were divided into two...
5.
Peng Y, Tu Q, Han Y, Wan C, Gao L
Exp Ther Med . 2023 Jun; 26(1):358. PMID: 37324515
Spinocerebellar ataxias (SCAs) are a group of autosomal dominant neurodegenerative diseases that are characterized by cerebellar ataxia. The most common types of SCAs are caused by polyglutamine (polyQ)-encoding cytosine-adenine-guanine repeat...
6.
Gao L, Huang W, Cai L, Peng Y
J Pain Res . 2022 Mar; 15:715-722. PMID: 35300403
Purpose: To assess Parkinson's disease (PD)-related pain using the Chinese translation of King's Parkinson's disease Pain Scale (KPPS). Patients And Methods: A cohort of 200 patients with primary PD was...
7.
Peng Y, Zhu M, Zheng J, Zhu Y, Li X, Wei C, et al.
BMC Neurol . 2015 Jul; 15:114. PMID: 26205240
Background: Late-onset multiple acyl-CoA dehydrogenase deficiency (MADD) is an autosomal recessive inherited disease of metabolic dysfunction clinically characterized by fluctuating proximal muscle weakness, excise intolerance, and dramatic riboflavin responsiveness. Dropped...
8.
Yang H, Wu J, Guo R, Peng Y, Zheng W, Liu D, et al.
Neural Regen Res . 2014 Sep; 8(14):1316-26. PMID: 25206426
Studies have shown that glycolysis increases during seizures, and that the glycolytic metabolite lactic acid can be used as an energy source. However, how lactic acid provides energy for seizures...
9.
Cai Q, Wu J, Qian Z, Peng Y, Cai J, Du Z
Se Pu . 2013 Jun; 31(3):200-5. PMID: 23785990
A new method has been developed using a hybrid triple-quadrupole linear ion trap (QTrap) mass spectrometer for the fast detection and identification of nine beta-agonists, clenbuterol, salbutamol, ractopamine, ritodrine, terbutaline,...
10.
Cai Q, Feng J, Zhang Y, Peng Y, Xue L, Du Z
Se Pu . 2011 Dec; 29(8):712-7. PMID: 22128732
A method was developed for the simultaneous determination and identification of 12 steroid hormone residues in pig tissues, including stanolone, aldosterone, boldenone, danazol, metandienone, methyltestosterone, nadrolone, norethindrone, progesterone, stanozolol, testosterone...