Qiao Wang

No. 1 Xi'anmen Street, West District
Beijing, 100034, China

Last Updated: 09/26/2026

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Found 25 publications

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

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

Journal: World journal of pediatrics : WJP

Published: February 02, 2017

Complex heterogeneity phenotypes and genotypes of glutaric aciduria type 1

Complex heterogeneity phenotypes and genotypes of glutaric aciduria type 1

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: May 12, 2016

Clinical and laboratory studies on four Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria

Clinical and laboratory studies on four Chinese patients with succinate-CoA ligase deficiency noticed by mild methylmalonic aciduria

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: May 05, 2016

Corrigendum to succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses [Gene 574(2015) 41-47].

Corrigendum to succinic semialdehyde dehydrogenase deficiency of four Chinese patients and prenatal diagnosis for three fetuses [Gene 574(2015) 41-47].

Journal: Gene

Published: April 15, 2016

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

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

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: August 28, 2015

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

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

Journal: European journal of medical genetics

Published: March 17, 2015

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

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

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics

Published: March 12, 2015

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

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

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics

Published: March 10, 2015

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

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

Journal: Gene

Published: February 17, 2015

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

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

Journal: Brain & development

Published: January 09, 2015

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

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

Journal: European journal of medical genetics

Published: December 01, 2014

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

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

Journal: Brain & development

Published: November 23, 2014

Showing 1-12 of 25

Last Updated: 09/26/2026