Tongli Han

Beijing, 100045, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 12 publications

A real-world study on the treatment of pediatric narcolepsy with pitolisant in China.

A real-world study on the treatment of pediatric narcolepsy with pitolisant in China.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: November 03, 2025

Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural history.

Phenotypic spectrum of iron-sulfur cluster assembly gene IBA57 mutations: c.286 T > C identified as a hotspot mutation in Chinese patients with a stable natural history.

Journal: Journal of human genetics

Published: March 10, 2024

Long-term effectiveness and tolerability of ketogenic diet therapy in patients with genetic developmental and epileptic encephalopathy onset within the first 6 months of life.

Long-term effectiveness and tolerability of ketogenic diet therapy in patients with genetic developmental and epileptic encephalopathy onset within the first 6 months of life.

Journal: Epilepsia open

Published: July 17, 2023

Functional connectivity differences in speech production networks in Chinese children with Rolandic epilepsy.

Functional connectivity differences in speech production networks in Chinese children with Rolandic epilepsy.

Journal: Epilepsy & behavior : E&B

Published: February 18, 2022

Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study.

Phenotypes and genotypes of mitochondrial diseases with mtDNA variations in Chinese children: A multi-center study.

Journal: Mitochondrion

Published: May 16, 2021

Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-up.

Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow-up.

Journal: Pediatric investigation

Published: March 28, 2021

Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study.

Age-dependent characteristics and prognostic factors of pediatric anti-N-methyl-d-aspartate receptor encephalitis in a Chinese single-center study.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: March 04, 2021

Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 Mutation.

Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 Mutation.

Journal: Frontiers in pharmacology

Published: January 03, 2019

Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in China.

Erratum to: The clinical and genetic characteristics in children with mitochondrial disease in China.

Journal: Science China. Life sciences

Published: July 22, 2017

The clinical and genetic characteristics in children with mitochondrial disease in China.

The clinical and genetic characteristics in children with mitochondrial disease in China.

Journal: Science China. Life sciences

Published: March 27, 2017

WITHDRAWN: Clinical and molecular analysis of six novel GALC mutations identified in 7 Chinese children with Krabbe disease.

WITHDRAWN: Clinical and molecular analysis of six novel GALC mutations identified in 7 Chinese children with Krabbe disease.

Journal: Brain & development

Published: March 22, 2017

Diagnosis of mitochondrial disorders in children with next generation sequencing

Diagnosis of mitochondrial disorders in children with next generation sequencing

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

Published: January 14, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026