Xin-hua Bao

Beijing, China

Last Updated: 09/26/2026

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Found 14 publications

The relationship between genotype and phenotype in Chinese children with glucose transporter type 1 deficiency syndrome.

The relationship between genotype and phenotype in Chinese children with glucose transporter type 1 deficiency syndrome.

Journal: Frontiers in neurology

Published: May 30, 2025

Clinical and genetic characteristics of glucose transporter 1 deficiency syndrome in a large cohort of Chinese patients.

Clinical and genetic characteristics of glucose transporter 1 deficiency syndrome in a large cohort of Chinese patients.

Journal: World journal of pediatrics : WJP

Published: December 07, 2024

Diagnosis and treatment recommendations for glucose transporter 1 deficiency syndrome.

Diagnosis and treatment recommendations for glucose transporter 1 deficiency syndrome.

Journal: World journal of pediatrics : WJP

Published: June 13, 2024

Paroxysmal crying and motor regression for more than two months in an infant

Paroxysmal crying and motor regression for more than two months in an infant

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

Published: April 25, 2019

Levetiracetam administration is correlated with lower mortality in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: a retrospective study.

Levetiracetam administration is correlated with lower mortality in patients with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes: a retrospective study.

Journal: Chinese medical journal

Published: January 26, 2019

Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization.

Analyses of Genotypes and Phenotypes of Ten Chinese Patients with Wolf-Hirschhorn Syndrome by Multiplex Ligation-dependent Probe Amplification and Array Comparative Genomic Hybridization.

Journal: Chinese medical journal

Published: March 11, 2016

Myoclonus epilepsy with ragged-red fibers: a case report and literature review

Myoclonus epilepsy with ragged-red fibers: a case report and literature review

Journal: Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

Published: December 19, 2015

STXBP1 gene mutation in newborns with refractory seizures

STXBP1 gene mutation in newborns with refractory seizures

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

Published: July 11, 2014

Long-term outcome and related factors of epileptic seizures in children

Long-term outcome and related factors of epileptic seizures in children

Journal: Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences

Published: April 19, 2014

Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome

Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome

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

Published: October 15, 2013

Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children

Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children

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

Published: March 27, 2013

Valproic acid-induced idiosyncratic liver injury in 4 cases

Valproic acid-induced idiosyncratic liver injury in 4 cases

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

Published: January 18, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026