Zhongbin Zhang
Tianjin, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Pleomorphic xanthoastrocytoma and treatment of epilepsy: a case report.
Journal: Translational pediatrics
Published: August 08, 2024
Analysis of the genotype-phenotype correlation in isovaleric acidaemia: A case report of long-term follow-up of a chinese patient and literature review.
Journal: Frontiers in neurology
Published: April 25, 2022
Brain Somatic Variant in Ras-Like Small GTPase RALA Causes Focal Cortical Dysplasia Type II.
Journal: Frontiers in behavioral neuroscience
Published: April 13, 2022
DNM1L-Related Mitochondrial Fission Defects Presenting as Encephalopathy: A Case Report and Literature Review.
Journal: Frontiers in pediatrics
Published: November 06, 2020
Genetic literacy series: clinical application of pharmacogenetics for adverse reactions to antiepileptic drugs.
Journal: Epileptic disorders : international epilepsy journal with videotape
Published: August 13, 2019
Somatic variants in new candidate genes identified in focal cortical dysplasia type II.
Journal: Epilepsia
Published: August 09, 2019
Genotypic Spectrum and Natural History of Cavitating Leukoencephalopathies in Childhood.
Journal: Pediatric neurology
Published: November 04, 2018
Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II.
Journal: Journal of neuroinflammation
Published: November 14, 2017
Similarities and differences between infantile and early childhood onset vanishing white matter disease.
Journal: Journal of neurology
Published: October 02, 2017
Distinct magnetic resonance imaging features in a patient with novel RARS2 mutations: A case report and review of the literature.
Journal: Experimental and therapeutic medicine
Published: December 16, 2016
Showing 1-10 of 10
Last Updated: 09/26/2026