Jianguang G. Tang

87 Xiangya Rd
Changsha, China

Last Updated: 09/26/2026

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Found 19 publications

Severe hyperhomocysteinemia due to MTHFR deficiency caused by a new mutation: A case report and literature review.

Severe hyperhomocysteinemia due to MTHFR deficiency caused by a new mutation: A case report and literature review.

Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
Published: January 09, 2025

Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature.

Clinical and radiological characteristics of adult-onset X-linked adrenoleukodystrophy: a Chinese cohort study and review of the literature.

Journal: BMC neurology
Published: October 24, 2024

Case report: Episodic psychosis caused by a novel SCP2 splicing mutation.

Case report: Episodic psychosis caused by a novel SCP2 splicing mutation.

Journal: Frontiers in neurology
Published: August 03, 2023

Case report: Desquamating dermatitis, bilateral cerebellar lesions in a late-onset methylmalonic acidemia patient.

Case report: Desquamating dermatitis, bilateral cerebellar lesions in a late-onset methylmalonic acidemia patient.

Journal: Frontiers in neurology
Published: July 08, 2023

Case Report: Diagnosis of Acute Q Fever With Aseptic Meningitis in a Patient by Using Metagenomic Next-Generation Sequencing.

Case Report: Diagnosis of Acute Q Fever With Aseptic Meningitis in a Patient by Using Metagenomic Next-Generation Sequencing.

Journal: Frontiers in medicine
Published: January 14, 2022

Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report.

Myasthenia gravis coexisting with HINT1-related motor axonal neuropathy without neuromyotonia: a case report.

Journal: BMC neurology
Published: August 20, 2021

Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series.

Clinical Presentations and Genetic Characteristics of Late-Onset MADD Due to ETFDH Mutations in Five Patients: A Case Series.

Journal: Frontiers in neurology
Published: July 26, 2021

Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China.

Mitochondrial genome variations are associated with amyotrophic lateral sclerosis in patients from mainland China.

Journal: Journal of neurology
Published: April 22, 2021

Mutation spectrum of amyotrophic lateral sclerosis in Central South China.

Mutation spectrum of amyotrophic lateral sclerosis in Central South China.

Journal: Neurobiology of aging
Published: March 10, 2021

Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified.

Molecular analysis of 53 Chinese families with Wilson's disease: Six novel mutations identified.

Journal: Molecular genetics & genomic medicine
Published: February 22, 2021

Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis.

Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis.

Journal: Frontiers in neurology
Published: February 02, 2021

The PARK2 Mutation Associated with Parkinson's Disease Enhances the Vulnerability of Peripheral Blood Lymphocytes to Paraquat.

The PARK2 Mutation Associated with Parkinson's Disease Enhances the Vulnerability of Peripheral Blood Lymphocytes to Paraquat.

Journal: BioMed research international
Published: June 17, 2020
Showing 1-12 of 19

Last Updated: 09/26/2026