Qiao Wang

发表

Pseudohypoaldosteronism Type II Caused by CUL3 Mutation Presented with Visual Impairment

C. Gong, B. Cao, Wen-jing Li, 2018, Chinese medical journal.

Succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses.

Shangzhi Huang, Yanling Yang, Yuan Ding, 2015, Gene.

Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduria

Yanling Yang, Yi Liu, Dongxiao Li, 2022, PloS one.

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

Yanling Yang, Dongxiao Li, Yuan Ding, 2018, World Journal of Pediatrics.

Five novel SUCLG1 mutations in three Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria

Yanling Yang, Yuan Ding, Jin-qing Song, 2016, Brain and Development.

First Chinese case of successful pregnancy with combined methylmalonic aciduria and homocystinuria, cblC type

Yanling Yang, Yuan Ding, Jin-qing Song, 2015, Brain and Development.

[Seven patients of argininemia with spastic tetraplegia as the first and major symptom and prenatal diagnosis of two fetuses with high risk].

Yanling Yang, Yuan Ding, Jin-qing Song, 2015, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy

Yanling Yang, Jin-qing Song, Yupeng Liu, 2012, Journal of pediatric endocrinology & metabolism : JPEM.

Analysis of the Mitochondrial Complex I-V Enzyme Activities of Peripheral Leukocytes in Oxidative Phosphorylation Disorders

Yanling Yang, Jin-qing Song, Yupeng Liu, 2011, Journal of child neurology.

[HEXB gene study and prenatal diagnosis for a family affected by infantile Sandhoff disease].

Yanling Yang, Yuan Ding, Jin-qing Song, 2013, Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences.

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

Zhi-long Wang, L. Zou, Yanling Yang, 2014, Brain and Development.

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

Yanling Yang, Yuan Ding, Jin-qing Song, 2013, Pediatric neurology.

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

L. Zou, Yanling Yang, Xiu-yu Shi, 2013, Mitochondrial DNA.

[Complex heterogeneity phenotypes and genotypes of glutaric aciduria type 1].

Yanling Yang, Qiao Wang, 2016, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Analysis of four Chinese patients with neonatal–onset isovaleric acidemia

Yuan Ding, Xi-yuan Li, Yupeng Liu, 2015 .

Five Chinese patients with 5-oxoprolinuria due to glutathione synthetase and 5-oxoprolinase deficiencies

Yanling Yang, Yuan Ding, Xi-yuan Li, 2015, Brain and Development.

Clinical and mutational spectra of 23 Chinese patients with glutaric aciduria type 1

Yanling Yang, Yuan Ding, Xi-yuan Li, 2014, Brain and Development.

Very long-chain acyl-coenzyme A dehydrogenase deficiency in Chinese patients: eight case reports, including one case of prenatal diagnosis.

Yanling Yang, Yuan Ding, Xi-yuan Li, 2015, European journal of medical genetics.

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

Yanling Yang, Xi-yuan Li, Yupeng Liu, 2014, Brain and Development.

The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1

Yanling Yang, Yuan Ding, Xi-yuan Li, 2015, Brain & development (Tokyo. 1979).

Eleven novel mutations of the BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease in the Chinese population: Report on eight cases.

Yanling Yang, Yuan Ding, Xi-yuan Li, 2015, European journal of medical genetics.

Genetic and biochemical findings in Chinese children with Leigh syndrome

L. Zou, Yanling Yang, Xi-yuan Li, 2013, Journal of Clinical Neuroscience.

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

Yu Liu, Yao Zhang, Qiao Wang, 2013, Mitochondrial DNA.

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

Yanling Yang, Yuan Ding, Xi-yuan Li, 2014, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

[Acute encephalopathy induced by vaccination in an infant with methylmalonic aciduria cblA].

Yanling Yang, Yuan Ding, Xi-yuan Li, 2015, Zhonghua er ke za zhi = Chinese journal of pediatrics.

Associations Between Sleep Duration, Wake-Up Time, Bedtime, and Abdominal Obesity: Results From 9559 Chinese Children Aged 7–18 Years

Di Wu, C. Gong, B. Cao, 2021, Frontiers in Endocrinology.

Comparing amniotic fluid mass spectrometry assays and amniocyte gene analyses for the prenatal diagnosis of methylmalonic aciduria

Yanling Yang, Yi Liu, Dongxiao Li, 2022, PloS one.