about
BSCL2 S90L mutation in a Chinese family with Silver syndrome with a review of the literature.Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.Abnormal baseline brain activity in Parkinson's disease with and without REM sleep behavior disorder: A resting-state functional MRI study.A clinical study of the coronal plane deformity in Parkinson disease.Clinical and neurophysiological features of familial cortical myoclonic tremor with epilepsy.Two cases of dural arteriovenous fistula presenting with parkinsonism and progressive cognitive dysfunction.Genetic analysis of the CHCHD2 gene in Chinese patients with familial essential tremor.Genetic analysis of the CHCHD2 gene in a cohort of Chinese patients with Parkinson disease.L-3-n-Butylphthalide Protects HSPB8 K141N Mutation-Induced Oxidative Stress by Modulating the Mitochondrial Apoptotic and Nrf2 Pathways.Huntington's Disease presenting with chorea of the ears.[Molecular genetics study of hereditary spastic paraplegia accompanied by distal amyotrophy-an update].Prevalence and clinical correlation of dysphagia in Parkinson disease: a study on Chinese patients.Altered brain network centrality in depressed Parkinson's disease patients.Fine mapping and whole-exome sequencing of a familial cortical myoclonic tremor with epilepsy family.[Familial cortical myoclonic tremor with epilepsy in a pedigree].Dramatic response to pyridoxine in a girl with absence epilepsy with ataxia caused by a de novo CACNA1A mutation.Genetic analysis of the TMEM230 gene in Chinese patients with familial Parkinson disease.Cervical spinal cord compression caused by X-linked hypophosphatemic rickets with a novel PHEX mutation.A Novel Homozygous Pathogenic Variant in a Chinese Patient with Pure Hereditary Spastic ParaplegiaLRP10 in autosomal-dominant Parkinson's diseaseEvaluation of MYORG mutations as a novel cause of primary familial brain calcificationNovel compound heterozygous ALS2 mutations in two Chinese siblings with infantile ascending hereditary spastic paralysisGenetic analysis of SPG4 and SPG3A genes in a cohort of Chinese patients with hereditary spastic paraplegiaHomozygous p.D331Y mutation in PLA2G6 in two patients with pure autosomal-recessive early-onset parkinsonism: further evidence of a fourth phenotype of PLA2G6-associated neurodegeneration[Genetic and clinical analysis in a Parkinson's disease family caused by expansion of SCA2]De novo mutation in DEPDC5 associated with unilateral pachygyria and intractable epilepsyQ10R mutation in SCN9A gene is associated with generalized epilepsy with febrile seizures plusIntronic pentanucleotide TTTCA repeat insertion in the SAMD12 gene causes familial cortical myoclonic tremor with epilepsy type 1Underestimated disease prevalence and severe phenotypes in patients with biallelic variants: A cohort study of primary familial brain calcification from China[Analysis of a patient with early-onset Parkinson's disease and PARK7 gene variation]A novel homozygous SYNJ1 mutation in two siblings with typical Parkinson's diseaseAlteration of Brain Functional Connectivity in Parkinson's Disease Patients with DysphagiaBiallelic loss-of-function mutations in JAM2 cause primary familial brain calcificationMYORG Mutation Heterozygosity Is Associated With Brain CalcificationIntronic (TTTGA)n insertion in SAMD12 also causes familial cortical myoclonic tremor with epilepsy[Silver syndrome: report of a family with 5 cases]
P50
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P50
description
researcher
@en
wetenschapper
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հետազոտող
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name
Zhidong Cen
@ast
Zhidong Cen
@en
Zhidong Cen
@es
Zhidong Cen
@nl
Zhidong Cen
@sl
type
label
Zhidong Cen
@ast
Zhidong Cen
@en
Zhidong Cen
@es
Zhidong Cen
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Zhidong Cen
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prefLabel
Zhidong Cen
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Zhidong Cen
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Zhidong Cen
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Zhidong Cen
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Zhidong Cen
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P1053
P-3410-2015
P106
P31
P3829
P496
0000-0003-3155-5781