Jianmin M. Zhong

Nanchang, China

Last Updated: 09/26/2026

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Found 26 publications

HMGB1-TLR4 signaling-mediated neuroinflammation contributes to the pathogenesis of infantile epileptic spasms syndrome in rats.

HMGB1-TLR4 signaling-mediated neuroinflammation contributes to the pathogenesis of infantile epileptic spasms syndrome in rats.

Journal: Frontiers in neurology

Published: April 07, 2026

Clinical application of HMGB1-TLR4 signaling pathway-mediated neuroinflammatory markers in infantile epileptic spasms syndrome.

Clinical application of HMGB1-TLR4 signaling pathway-mediated neuroinflammatory markers in infantile epileptic spasms syndrome.

Journal: Frontiers in immunology

Published: February 01, 2026

LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study.

LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study.

Journal: Frontiers in neurology

Published: October 20, 2025

Nusinersen effectiveness and safety in children with type II/III 5q-spinal muscular atrophy: Second interim analysis from a Chinese disease registry.

Nusinersen effectiveness and safety in children with type II/III 5q-spinal muscular atrophy: Second interim analysis from a Chinese disease registry.

Journal: Chinese medical journal

Published: August 30, 2025

Identification of a de Novo MARK2 gene variant in a patient with autism spectrum disorder, epilepsy, and neurodevelopmental delay.

Identification of a de Novo MARK2 gene variant in a patient with autism spectrum disorder, epilepsy, and neurodevelopmental delay.

Journal: Neurogenetics

Published: March 26, 2025

Identification of Compound Heterozygous Variants in OBSCN Gene Associated With Rhabdomyolysis: A Case Report.

Identification of Compound Heterozygous Variants in OBSCN Gene Associated With Rhabdomyolysis: A Case Report.

Journal: Molecular genetics & genomic medicine

Published: December 17, 2024

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Mutations in the spliceosomal gene SNW1 cause neurodevelopment disorders with microcephaly.

Journal: The Journal of clinical investigation

Published: August 20, 2024

Identification of novel BCL11A variant in a patient with developmental delay and behavioural differences.

Identification of novel BCL11A variant in a patient with developmental delay and behavioural differences.

Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Published: July 10, 2024

Administration practices of and adherence to nusinersen in children with spinal muscular atrophy: a multicenter disease registry study in China.

Administration practices of and adherence to nusinersen in children with spinal muscular atrophy: a multicenter disease registry study in China.

Journal: BMC pediatrics

Published: March 29, 2024

Nusinersen effectiveness and safety in pediatric patients with 5q-spinal muscular atrophy: a multi-center disease registry in China.

Nusinersen effectiveness and safety in pediatric patients with 5q-spinal muscular atrophy: a multi-center disease registry in China.

Journal: Journal of neurology

Published: February 21, 2024

A newborn with convulsions 12 days after birth was misdiagnosed as neonatal intracranial hemorrhage: Case report.

A newborn with convulsions 12 days after birth was misdiagnosed as neonatal intracranial hemorrhage: Case report.

Journal: Medicine

Published: January 11, 2024

Identification of a novel METTL23 gene variant in a patient with an intellectual development disorder: a literature review and case report.

Identification of a novel METTL23 gene variant in a patient with an intellectual development disorder: a literature review and case report.

Journal: Frontiers in pediatrics

Published: October 26, 2023

Showing 1-12 of 26

Last Updated: 09/26/2026