Jin-qing Song

Beijing, China

Last Updated: 09/26/2026

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Found 22 publications

Case report: An asymptomatic mother with an inborn error of cobalamin metabolism (cblC) detected through high homocysteine levels during prenatal diagnosis.

Case report: An asymptomatic mother with an inborn error of cobalamin metabolism (cblC) detected through high homocysteine levels during prenatal diagnosis.

Journal: Frontiers in nutrition
Published: December 28, 2022

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

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

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: November 28, 2018

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

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

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

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: May 12, 2016

Psychomotor retardation and intermitent convulsions for 8 months in an infant

Psychomotor retardation and intermitent convulsions for 8 months in an infant

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: January 20, 2016

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

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

Journal: Neurochemical research
Published: December 20, 2015

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

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

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: October 21, 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

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

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

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: June 14, 2014

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

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

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: February 06, 2014

Methylenetetrahydrofolate reductase deficiency-induced schizophrenia in a school-age boy

Methylenetetrahydrofolate reductase deficiency-induced schizophrenia in a school-age boy

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: January 28, 2014

A boy with Fabry disease with the onset at the age of four

A boy with Fabry disease with the onset at the age of four

Journal: Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences
Published: April 18, 2013
Showing 1-12 of 22

Last Updated: 09/26/2026