Full Text Journal Articles by
Author Xi Yuan Li

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[Reye syndrome and sudden death symptoms after oral administration of nimesulide due to upper respiratory tract infection in a boy].

Li-Fang Feng, Xiao-Hong Chen, Dong-Xiao Li, Xi-Yuan Li, Jin-Qing Song, Ying Jin, Yan-Ling Yang,

A boy aged 6 years and 3 months developed upper respiratory tract infection and pyrexia 2 months ago and was given oral administration of nimesulide by his parents according to directions. Half an hour later, the boy experienced convulsions and cardiopulmonary arrest, and emergency examination found hypoketotic hypoglycemia, metabolic acidosis, ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2018, 20(11):944-949]

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Alopecia Areata is Associated with Increased Expression of Heart Disease Biomarker Cardiac Troponin I.

Eddy Hsi Wang, Leopoldo Santos, Xi Yuan Li, Annie Tran, Sandra S Y Kim, Katrina Woo, Jerry Shapiro, Kevin J McElwee,

The development of androgenetic alopecia is associated with a risk of developing cardiovascular diseases, but the association of alopecia areata with cardiovascular diseases in humans is largely unexplored. We measured the plasma level of two common cardiovascular disease markers, cardiac troponin I and C-reactive protein, in alopecia areata and androgenetic ... Read more >>

Acta Derm. Venereol. (Acta dermato-venereologica)
[2018, 98(8):776-782]

Cited: 2 times

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Clinical, Biochemical, and Genetic Findings of Cystinuria in Chinese Children.

Yan-Yan Ma, Yu-Peng Liu, Dongxiao Li, Xi-Yuan Li, Jin-Qing Song, Yan-Ling Yang,

BACKGROUND:Cystinuria is a rare inherited renal stone disease caused by mutations in the SLC3A1 and SLC7A9 genes. The Chinese cystinuria phenotype and genotype have rarely been reported in the literature. METHODS:For this research, the clinical features and genetic etiology were analyzed in seven children, and the clinical characteristics were summarized. ... Read more >>

Clin. Lab. (Clinical laboratory)
[2018, 64(7):1145-1151]

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Clinical, biochemical, and genetic analysis of the mitochondrial respiratory chain complex I deficiency.

Yan-Yan Ma, Xi-Yuan Li, Zhi-Qin Li, Ji-Qing Song, Jing Hou, Jian-Hua Li, Li Sun, Jun Jiang, Yan-Ling Yang,

Mitochondrial respiratory chain complex I deficiency is one of common mitochondrial disorders. However, the information is relatively little about the features of Chinese patients. In this study, the clinical, biological, and genetic analyses were performed in the children with respiratory chain complex I deficiency, in order to further understand the ... Read more >>

Medicine (Baltimore) (Medicine)
[2018, 97(32):e11606]

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Eight novel mutations of CBS gene in nine Chinese patients with classical homocystinuria.

Dong-Xiao Li, Xi-Yuan Li, Hui Dong, Yu-Peng Liu, Yuan Ding, Jin-Qing Song, Ying Jin, Yao Zhang, Qiao Wang, Yan-Ling Yang,

BACKGROUND:Classical homocystinuria (homocysteinemia type 1, MIM# 236200) is a rare inherited disorder in Mainland China. This study aimed to identify mutations in the cystathionine β-synthase (CBS) gene which are associated with classical homocystinuria in nine Chinese patients. METHODS:Nine Chinese patients were diagnosed at the age of 5 years 4 months to 18 years ... Read more >>

World J Pediatr (World journal of pediatrics : WJP)
[2018, 14(2):197-203]

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[Rapid determination of nine components in the first extraction process of Xingnaojing injection by using ultraviolet spectroscopy].

Kai-Yi Huang, Dan-Ni Wei, Jin-Yang Fang, Xi-Yuan Li, Bin-Jun Yan,

In this study, an analytical method based on ultraviolet spectroscopy was established for the rapid determination of nine components including isophorone, 4-methylene-isophorone, curcumenone, curcumenol, curdione, curzerenone, furanodienone, curcumol and germacrone in the first extraction process of Xingnaojing injection. 166 distillate samples of Gardeniae Fructus and Radix Curcumae were collected in ... Read more >>

Zhongguo Zhong Yao Za Zhi (Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica)
[2017, 42(19):3755-3760]

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[Psychomotor retardation and intermitent convulsions for 8 months in an infant].

Yuan Ding, Xi-Yuan Li, Yu-Peng Liu, Dong-Xiao Li, Jin-Qing Song, Meng-Qiu Li, Ya-Ping Qin, Tong-Fei Wu, Yan-Ling Yang,

This study reports a boy with psychomotor retardation and epilepsy due to maternal phenylketonuria (PKU). The boy was admitted at the age of 20 months because of psychomotor retardation and epilepsy. He had seizures from the age of 1 year. His development quotient was 43. He presented with microcephaly, normal ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2016, 18(1):67-71]

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[Acute brainstem encephalitis and myelitis in a girl with isolated methylmalonic aciduria due to MUT gene defect].

Yu-Peng Liu, Yuan Ding, Xi-Yuan Li, Hai-Jun Wang, Jin-Qing Song, Jin-Tang Ye, Tong-Fei Wu, Yan-Ling Yang,

Methylmalonyl CoA mutase deficiency due to MUT gene defect has been known as the main cause of isolated methylmalonic acidemia in Mainland China. This study reported a patient with isolated methylmalonic aciduria (MUT type) characterized as acute brainstem encephalitis and myelitis. The previously healthy girl presented with fever, lethargy and ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2015, 17(10):1103-1106]

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[A Chinese boy with methylmalonic aciduria cblB type and a novel mutation in the MMAB gene].

Yu-Peng Liu, Hai-Jun Wang, Tong-Fei Wu, Xi-Yuan Li, Jin-Qing Song, Yuan Ding, Yao Zhang, Qiao Wang, Yan-Ling Yang,

cblB defect is a rare type of methylmalonic aciduria. In this study, a Chinese boy was diagnosed with methylmalonic aciduria cblB type and a novel mutation in the MMAB gene. The clinical presentations, blood acylcarnitines profiles, urine organic acids and genetic features of the patient were reported. The boy presented ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2015, 17(2):172-175]

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[Clinical and ATP7A gene analysis of three infants with Menkes disease and prenatal diagnosis for a fetus at risk].

Qiao Wang, Yuan Ding, Jing-Min Wang, Qiong-Hui Huang, Cheng-Feng Zhao, Yu-Peng Liu, Xi-Yuan Li, Tong-Fei Wu, Jin-Qing Song, Yu-Jie Wang, Yan-Ling Yang,

Menkes disease is a rare X-linked recessive disorder characterized by multi-systemic disorder of copper deficiency caused by ATP7A gene mutation. In this study, the clinical and laboratory features of three patients with Menkes disease were analyzed. Prenatal diagnosis had been performed for a fetus of a family. Three patients were ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2014, 16(6):624-628]

Cited: 1 time

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Microvesicles mediate transfer of P-glycoprotein to paclitaxel-sensitive A2780 human ovarian cancer cells, conferring paclitaxel-resistance.

Fang-fang Zhang, Yi-fei Zhu, Qian-nan Zhao, Dan-tong Yang, Ye-ping Dong, Li Jiang, Wei-xing Xing, Xi-yuan Li, Hui Xing, Mei Shi, Yun Chen, Iain C Bruce, Jian Jin, Xin Ma,

The overexpression of P-glycoprotein (P-gp) causes resistance to chemotherapy in human ovarian cancer. However, the underlying mechanism remains unclear. In the present study, we showed that, at membrane-bound protein level, P-gp was 'shared' between human ovarian cancer cells by the intercellular transfer of microvesicles (MVs). Paclitaxel-resistant human ovarian cancer cells ... Read more >>

Eur. J. Pharmacol. (European journal of pharmacology)
[2014, 738:83-90]

Cited: 22 times

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[Methylenetetrahydrofolate reductase deficiency-induced schizophrenia in a school-age boy].

Qiao Wang, Jing Liu, Yu-Peng Liu, Xi-Yuan Li, Yan-Yan Ma, Tong-Fei Wu, Yuan Ding, Jin-Qing Song, Yu-Jie Wang, Yan-Ling Yang,

Methylenetetrahydrofolate reductase (MTHFR) deficiency is a rare autosomal recessive disorder. It is known that MTHFR deficiency may result in hyperhomocysteinemia, but MTHFR deficiency-induced schizophrenia has been rarely reported. Here we present the clinical course, biochemical and genetic characteristics of schizophrenia resulted from MTHFR deficiency in a school-age boy. He was ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2014, 16(1):62-66]

Cited: 4 times

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[A boy with Fabry disease with the onset at the age of four].

Yu-peng Liu, Yu Huang, Qiao Wang, Tong-fei Wu, Yan-yan Ma, Xi-yuan Li, Jin-qing Song, Yan-ling Yang,

Fabry disease is an X-linked recessive lysosomal storage disorder caused by a deficiency of α-galactosidase A (GLA). Intracellular accumulation of globotriaosylceramide, the glycolipid substrate of this enzyme, leads to severe painful neuropathy with progressive renal, cardiovascular, and cerebrovascular dysfunction. Patients of severe cases die young. It has been proved that ... Read more >>

Beijing Da Xue Xue Bao (Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences)
[2013, 45(2):307-311]

Cited: 1 time

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[Clinical, biochemical and genetic analysis of the mitochondrial disorders presenting with cardiac damage].

Yan-yan Ma, Tong-fei Wu, Yu-peng Liu, Qiao Wang, Xi-yuan Li, Yuan Ding, Jin-qing Song, Yan-ling Yang,

Mitochondrial disease is a group of energy metabolic disorders, characterized by involvement of multisystem with high energy requirements. Encephalomyopathies are common clinical findings of the mitochondrial diseases. However, mitochondrial cardiac damage is not rare. In this study, the clinical, biological, and genetic analyses were performed in three patients with mitochondrial ... Read more >>

Zhonghua Er Ke Za Zhi (Zhonghua er ke za zhi = Chinese journal of pediatrics)
[2013, 51(12):909-914]

Cited: 0 times

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Prenatal diagnosis of citrullinemia type 1: a Chinese family with a novel mutation of the ASS1 gene.

Tong-Fei Wu, Yu-Peng Liu, Xi-Yuan Li, Qiao Wang, Jin-Qing Song, Yan-Ling Yang,

BACKGROUND: Argininosuccinate synthetase deficiency (citrullinemia type 1) is a rare autosomal recessive disorder of the urea cycle characterized by elevated concentrations of citrulline, ammonia, and orotic acid, manifesting with acute hyperammonemic crises, usually early in life, with concurrent neurologic deterioration. Only a few cases of citrullinemia type 1 have been ... Read more >>

Brain Dev. (Brain & development)
[2014, 36(3):264-267]

Cited: 4 times

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Heterogeneity of six children and their mothers with mitochondrial DNA 3243 A>G mutation.

Yan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, Qiao Wang, Xi-Yuan Li, Jin-Qing Song, Xiu-Yu Shi, Wei-Na Zhang, Meng Zhao, Ling-Yan Hu, Yan-Ling Yang, Li-Ping Zou,

To study the clinical, biochemical, and genetic heterogeneity of six Chinese patients and their mothers with the 3243 A>G mutation, six patients (ranging from 5 to 11 years) were hospitalized. All the mothers were healthy. Mitochondrial respiratory chain enzyme activities were determined by spectrophotometry. Mitochondrial gene was analyzed in all ... Read more >>

Mitochondrial DNA (Mitochondrial DNA)
[2013, 24(3):297-302]

Cited: 3 times

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Genetic and biochemical findings in Chinese children with Leigh syndrome.

Yan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, Qiao Wang, Jin-Qing Song, Xi-Yuan Li, Xiu-Yu Shi, Wei-Na Zhang, Meng Zhao, Lin-Yan Hu, Yan-Ling Yang, Li-Ping Zou,

This study investigated the genetic and enzymological features of Leigh syndrome due to respiratory chain complex deficiency in Chinese patients. The clinical features of 75 patients were recorded. Mitochondrial respiratory chain enzyme activities were determined via spectrophotometry. Mitochondrial gene sequence analysis was performed in 23 patients. Five core pedigrees were ... Read more >>

J Clin Neurosci (Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia)
[2013, 20(11):1591-1594]

Cited: 7 times

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Five novel mutations in ARG1 gene in Chinese patients of argininemia.

Tong-Fei Wu, Yu-Peng Liu, Xi-Yuan Li, Qiao Wang, Yuan Ding, Yan-Yan Ma, Jin-Qing Song, Yan-Ling Yang,

BACKGROUND: Argininemia is an autosomal recessive genetic disorder caused by hepatocyte arginase deficiency. It could be detected by blood amino acids analysis (high arginine) and confirmed by molecular diagnosis. The clinical manifestations in patients are similar to cerebral palsy so the diagnosis is usually much delayed. Reports of argininemia from ... Read more >>

Pediatr. Neurol. (Pediatric neurology)
[2013, 49(2):119-123]

Cited: 5 times

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Two compound frame-shift mutations in succinate dehydrogenase gene of a Chinese boy with encephalopathy.

Yan-Yan Ma, Tong-Fei Wu, Yu-Peng Liu, Qiao Wang, Xi-Yuan Li, Yuan Ding, Jin-Qing Song, Xiu-Yu Shi, Wei-Na Zhang, Meng Zhao, Ling-Yan Hu, Jun Ju, Zhi-Long Wang, Yan-Ling Yang, Li-Ping Zou,

OBJECTIVE: To investigate respiratory chain complex II deficiency resulted from mutation in succinate dehydrogenase gene (SDH) encoding complex II subunits in China. METHODS: An 11-year-old boy was admitted to our hospital. He had a history of progressive psychomotor regression and weakness since the age of 4years. His cranial magnetic resonance ... Read more >>

Brain Dev. (Brain & development)
[2014, 36(5):394-398]

Cited: 7 times

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[Mitochondrial disorders associated with mitochondrial respiratory chain complex V deficiency].

Xi-Yuan Li, Yan-Ling Yang,

The mammalian mitochondrial ATP synthase, also as known as mitochondrial respiratory chain complex V, is a large protein complex located in the mitochondrial inner membrane, where it catalyzes ATP synthesis from ADP, Pi, and Mg2+ at the expense of an electrochemical gradient of protons generated by the electron transport chain. ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2013, 15(7):596-600]

Cited: 3 times

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[Abnormal findings during newborn period of 160 patients with early-onset methylmalonic aciduria].

Yu-peng Liu, Yan-yan Ma, Tong-fei Wu, Qiao Wang, Xi-yuan Li, Yuan Ding, Jin-qing Song, Yu Huang, Yan-ling Yang,

Methylmalonic aciduria is the most common disorder of organic acidurias in the mainland of China. It is also the one of treatable metabolic disorders. The clinical spectrum of the patients varies from severe neonatal-onset forms with neonatal brain injury and high mortality to milder forms with adult-onset. The clinical manifestations ... Read more >>

Zhonghua Er Ke Za Zhi (Zhonghua er ke za zhi = Chinese journal of pediatrics)
[2012, 50(6):410-414]

Cited: 2 times

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[Intrahepatic cholestasis due to mitochondrial respiratory chain complex I deficiency in a Chinese boy].

Tong-Fei Wu, Yu-Peng Liu, Qiao Wang, Xi-Yuan Li, Yan-Yan Ma, Jin-Qing Song, Yan-Ling Yang,

Mitochondrial respiratory chain deficiency is a common cause of mitochondrial disease in children. This study aimed to review the clinical, enzymatic and genetic characteristics of a Chinese boy with progressive intrahepatic cholestasis due to mitochondrial respiratory chain complex I deficiency. The boy developed diarrhea from the age of 13 months, ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2012, 14(4):241-246]

Cited: 0 times

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Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency.

Yan Yan Ma, Tong Fei Wu, Yu Peng Liu, Qiao Wang, Xi Yuan Li, Yao Zhang, Jin Qing Song, Yu Jie Wang, Yan Ling Yang,

Mitochondrial respiratory chain complex I enzyme deficiency is the most commonly seen mitochondrial respiratory chain disorder. Although screening and diagnostic methods are available overseas, clinically feasible diagnostic methods have not yet been established in China. In this study, four Chinese boys with Leigh syndrome due to complex I deficiency were ... Read more >>

Mitochondrial DNA (Mitochondrial DNA)
[2013, 24(1):67-73]

Cited: 4 times

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[Corpus of biochemical changes after death by potassium intoxication in rabbits].

Xin-ju Zhu, Xi-yuan Li, Kai Li, Li-ping Chen, Yong Ke, Zhen-yuan Wang,

OBJECTIVE: To explore the objective evidence of the corpus biochemical changes in rabbits for postmortem diagnosis of potassium intoxication. METHODS: Rabbits were sacrificed by Infusion of 0.3% KCl at full speed push or 1% KCl at 100 drip/min, respectively, with normal rabbits used as control. Cardiac blood and urine samples ... Read more >>

Fa Yi Xue Za Zhi (Fa yi xue za zhi)
[2007, 23(4):244-6, 249]

Cited: 0 times

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[Retrospective analysis of drug treatment on inpatients with chronic heart failure].

Jin-ping Ma, Lin Wang, Qun Dang, Yong-jian Li, Xi-yuan Li, Cheng-zong Zhang, Guang-ping Li,

OBJECTIVE: To investigate drug treatment of inpatients with chronic heart failure(CHF) during the past 30 years in some areas and to provide more information on the treatment strategy of CHF. METHODS: In two centers a retrospective study was conducted. All data were taken from the hospitalized cases with chronic heart ... Read more >>

Zhonghua Liu Xing Bing Xue Za Zhi (Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi)
[2007, 28(1):78-82]

Cited: 1 time

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