Feixia Zhan

600 Yishan Road
Shanghai, 200233, China

Last Updated: 09/26/2026

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Found 14 publications

Novel proteomics and neuropathology of NOTCH2NLC-related neuronal intranuclear inclusion disease.

Novel proteomics and neuropathology of NOTCH2NLC-related neuronal intranuclear inclusion disease.

Journal: Frontiers in aging neuroscience

Published: March 10, 2026

A Charcot-Marie-Tooth Disease Type 1J Case With Diffuse Thickening of Peripheral Nerves.

A Charcot-Marie-Tooth Disease Type 1J Case With Diffuse Thickening of Peripheral Nerves.

Journal: Neurology

Published: January 21, 2025

The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China.

The Phenotypic and Genotypic Spectrum of CSF1R-Related Disorder in China.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 18, 2023

Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum.

Episodic Neurological Dysfunction in X-Linked Charcot-Marie-Tooth Disease: Expansion of the Phenotypic and Genetic Spectrum.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: March 17, 2023

Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series.

Heterogeneous Clinical Phenotypes of dHMN Caused by Mutation in HSPB1 Gene: A Case Series.

Journal: Biomolecules

Published: August 12, 2022

Clinical heterogeneity in a family with flail arm syndrome and review of hnRNPA1-related spectrum.

Clinical heterogeneity in a family with flail arm syndrome and review of hnRNPA1-related spectrum.

Journal: Annals of clinical and translational neurology

Published: July 27, 2022

Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia.

Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia.

Journal: Journal of neurology

Published: November 23, 2021

Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene.

Generation of an human induced pluripotent stem cell JTUi007-A from a patient with CSF1R-related leukoencephalopathy carrying heterozygous p.Ile794Thr mutation in CSF1R gene.

Journal: Stem cell research

Published: September 03, 2021

Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome.

Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome.

Journal: Metabolic brain disease

Published: July 31, 2021

A report of two cases of bulbospinal form Alexander disease and preliminary exploration of the disease.

A report of two cases of bulbospinal form Alexander disease and preliminary exploration of the disease.

Journal: Molecular medicine reports

Published: December 15, 2020

Late-onset autoimmune polyendocrine syndrome type 1: a case report and literature review.

Late-onset autoimmune polyendocrine syndrome type 1: a case report and literature review.

Journal: Immunologic research

Published: November 14, 2020

Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1-Related Hyperekplexia.

Excessive Startle with Novel GLRA1 Mutations in 4 Chinese Patients and a Literature Review of GLRA1-Related Hyperekplexia.

Journal: Journal of clinical neurology (Seoul, Korea)

Published: July 19, 2019

Showing 1-12 of 14

Last Updated: 09/26/2026