Zhi-dong Cen - Publications

Genetic profile of Chinese patients with Charcot-Marie-Tooth disease.

Journal: Chinese medical journal

Published: September 17, 2020

A novel homozygous SYNJ1 mutation in two siblings with typical Parkinson's disease.

Journal: Parkinsonism & related disorders

Published: August 07, 2019

L-3-n-Butylphthalide Protects HSPB8 K141N Mutation-Induced Oxidative Stress by Modulating the Mitochondrial Apoptotic and Nrf2 Pathways.

Journal: Frontiers in neuroscience

Published: March 03, 2017

Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.

Journal: Seizure

Published: September 03, 2015

Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.

Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Published: March 11, 2015

Cervical spinal cord compression caused by X-linked hypophosphatemic rickets with a novel PHEX mutation.

Journal: Neurology India

Published: September 20, 2014

Novel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysis.

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

Published: September 15, 2014

Molecular genetics study of hereditary spastic paraplegia accompanied by distal amyotrophy-an update

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 09, 2013

Silver syndrome: report of a family with 5 cases

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: August 09, 2013