Tong-fei F. Wu

Beijing, 100034, China

Last Updated: 09/26/2026

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Found 17 publications

Heterogeneous phenotypes, genotypes, treatment and prevention of 1 003 patients with methylmalonic acidemia in the mainland of China

Heterogeneous phenotypes, genotypes, treatment and prevention of 1 003 patients with methylmalonic acidemia in the mainland of China

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: June 11, 2018

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

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

Advances in clinical and molecular genetics studies on argininemia

Advances in clinical and molecular genetics studies on argininemia

Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: November 16, 2013

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

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

Journal: Pediatric neurology
Published: January 07, 2013

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

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

Journal: Brain & development
Published: December 17, 2012

Genetic and biochemical findings in Chinese children with Leigh syndrome.

Genetic and biochemical findings in Chinese children with Leigh syndrome.

Journal: Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia
Published: October 27, 2012

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

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

Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: August 31, 2012
Showing 1-12 of 17

Last Updated: 09/26/2026