Full Text Journal Articles by
Author Jin Qing Song

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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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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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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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Effect of a 12-Week Aerobic Exercise Training on Serum Fetuin-A and Adipocytokine Levels in Type 2 Diabetes.

Ling-Yun Zhang, Tao Liu, Ya-Qin Teng, Xiao-Yan Yao, Tian-Tian Zhao, Liang-Yan Lin, Qing-Song Jin, Yong-Jun Jin,

OBJECTIVE:We aimed to evaluate the effect of 12-week aerobic exercise training on fetuin-A levels in type 2 diabetes mellitus and examine the relationships between fetuin-A and adipocytokine levels and cardiovascular risk factors. METHODS:The study included 32 patients with type 2 diabetes mellitus who were assigned to an exercise or a ... Read more >>

Exp. Clin. Endocrinol. Diabetes (Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association)
[2018, 126(8):487-492]

Cited: 4 times

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Treatment with Isorhamnetin Protects the Brain Against Ischemic Injury in Mice.

Jin-Jing Zhao, Jin-Qing Song, Shu-Yi Pan, Kai Wang,

Ischemic stroke is a major cause of morbidity and mortality, yet lacks effective neuroprotective treatments. The aim of this work was to investigate whether treatment with isorhamnetin protected the brain against ischemic injury in mice. Experimental stroke mice underwent the filament model of middle cerebral artery occlusion with reperfusion. Treatment ... Read more >>

Neurochem. Res. (Neurochemical research)
[2016, 41(8):1939-1948]

Cited: 6 times

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[Limb torsion and developmental regression for one month after hand, foot and mouth disease in an infant].

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

A one-year-old girl visited the hospital due to limb torsion and developmental regression for one month after hand, foot and mouth disease. At the age of 11 months, she visited a local hospital due to fever for 5 days and skin rash with frequent convulsions for 2 days and was ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2016, 18(5):426-430]

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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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[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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[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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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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Association between resistin +299A/A genotype and nonalcoholic fatty liver disease in Chinese patients with type 2 diabetes mellitus.

Ling-Yun Zhang, Yong-Jun Jin, Qing-Song Jin, Liang-Yan Lin, Dong-Dong Zhang, Li-Li Kong,

OBJECTIVE: To investigate the relationship between the resistin intronic +299G/A polymorphism and nonalcoholic fatty liver disease (NAFLD) in patients with type 2 diabetes mellitus (T2DM). METHODS: We selected 738 T2DM patients, including 395 with NAFLD and 343 without fatty liver disease, as well as 279 healthy control individuals, and analyzed ... Read more >>

Gene (Gene)
[2013, 529(2):340-344]

Cited: 11 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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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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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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[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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[Skin lesions induced by malnutrition in an infant with methylmalonic aciduria and homocysteic acidemia].

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

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2012, 14(3):233-234]

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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[Mitochondrial respiratory chain complex I deficiency due to 10191T>C mutation in ND3 gene].

Yu-Peng Liu, Yan-Yan Ma, Tong-Fei Wu, Qiao Wang, Qing-Peng Kong, Xiao-Qiong Wei, Yao Zhang, Jin-Qing Song, Xing-Zhi Chang, Yue-Hua Zhang, Jiang-Xi Xiao, Yan-Ling Yang,

This study reviews a case of mitochondrial respiratory chain complex I deficiency due to the 10191T>C mutation in mitochondrial ND3 gene. The previously healthy boy progressively presented with blepharoptosis, weakness, epilepsy and motor regression at age 6 years. Elevated blood lactate and pyruvate were observed. Brain magnetic resonance imaging showed ... Read more >>

Zhongguo Dang Dai Er Ke Za Zhi (Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics)
[2012, 14(8):561-566]

Cited: 3 times

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[Enzyme analysis of isolated mitochondrial respiratory chain complex III deficiency].

Yan-yan Ma, Tong-fei Wu, Yu-peng Liu, Qiao Wang, Jin-qing Song, Jiang-xi Xiao, Yu-wu Jiang, Yan-ling Yang,

To study the clinical and enzymological characteristics of the children with mitochondrial respiratory chain complex III deficiency.The clinical manifestations of five patients (3 males, 2 females) were summarized. Spectrophotometric assay was used for the analysis of respiratory chain complex I to V enzyme activity in peripheral blood leukocytes, after obtaining ... Read more >>

Zhonghua Er Ke Za Zhi (Zhonghua er ke za zhi = Chinese journal of pediatrics)
[2011, 49(11):848-852]

Cited: 0 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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