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Zhanfang Sun

Central South University

16

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110

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Identification of Alzheimer’s disease–associated rare coding variants in the ECE2 gene

2020 JCI insight
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Research progress of diagnosis and treatment of dystonia

2017 Chinese Journal of Contemporary Neurology and Neurosurgery
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Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population

2017 International Journal of Neuroscience
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C9orf72 hexanucleotide expansion analysis in Chinese patients with multiple system atrophy.

2015 Parkinsonism & Related Disorders
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High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression

2015 The Cerebellum
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SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population.

2015 International Journal of Neuroscience
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Increase of the plasma α‐synuclein levels in patients with multiple system atrophy

2014 Movement Disorders
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Genetic Diagnosis of Two Dopa-Responsive Dystonia Families by Exome Sequencing

2014 PLOS ONE
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Delayed encephalopathy with movement disorder and catatonia: A rare combination after wasp stings

2013 Clinical Neurology and Neurosurgery
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A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau disease.

2013 Journal of Clinical Neuroscience
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Citations (6)