Search Results - "Gan, Shi-Rui"

"Phoenix in Flight": an unique fruit morphology ensures wind dispersal of seeds of the phoenix tree (Firmiana simplex (L.) W. Wight).

Authors: Gan, Shi-Rui Guo, Jun-Cheng Zhang, Yun-Xiao et al.

Source: BMC Plant Biology. 3/12/2022, Vol. 22 Issue 1, p1-12. 12p.

Fatigue in the Preataxic and Ataxic Stages of Spinocerebellar Ataxia Type 3.

Authors: Chen, Zhi‐li Xiao, Li‐mei Li, Chun et al.

Source: European Journal of Neurology. Apr2025, Vol. 32 Issue 4, p1-8. 8p.

Subjects: Fatigue (Physiology), Spinocerebellar ataxia, Quality of life, Neuroanatomy, Magnetic resonance imaging, Disease progression

Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado–Joseph disease Patients.

Authors: Chen, Sheng Gan, Shi‐Rui Cai, Ping‐Ping et al.

Source: CNS Neuroscience & Therapeutics. Jan2016, Vol. 22 Issue 1, p38-42. 5p. 2 Charts, 2 Graphs.

Population Genetics and New Insight into Range of CAG Repeats of Spinocerebellar Ataxia Type 3 in the Han Chinese Population.

Authors: Gan, Shi-Rui Ni, Wang Dong, Yi et al.

Source: PLoS ONE. 8/12/2015, Vol. 10 Issue 8, p1-12. 12p.

Dysarthria in Spinocerebellar Ataxia Type 3: Prevalence and Disease Progression.

Authors: Ji, Hai-Ping Cui, Mao-Lin Lin, Wei et al.

Source: Journal of Speech, Language & Hearing Research. Sep2025, Vol. 68 Issue 9, p4256-4262. 7p.

Subject Terms: *Dysarthria, *Data analysis, *Retrospective studies, Spinocerebellar ataxia, Genomics, T-test (Statistics), Research funding, Polymerase chain reaction, Interviewing, Multiple regression analysis, DNA, Chi-squared test, Mann Whitney U Test, Descriptive statistics, Statistics, Health outcome assessment, Data analysis software, Disease progression, Disease risk factors, Disease complications

Multidimensional abnormal gait analysis and biomarker identification for patients with spinocerebellar ataxia type 3 using an Azure Kinect-based motion capture system.

Authors: Cui, Mao-Lin Pan, Li-Ying Lin, Wei et al.

Source: Gait & Posture. Jan2026, Vol. 123, pN.PAG-N.PAG.

The impact of ethnicity on the clinical presentations of spinocerebellar ataxia type 3.

Authors: Gan, Shi-Rui Figueroa, Karla P. Xu, Hao-Ling et al.

Source: Parkinsonism & Related Disorders. Mar2020, Vol. 72, p37-43. 7p.

Hispanic Spinocerebellar Ataxia Type 35 (SCA35) with a Novel Frameshift Mutation.

Authors: Lin, Chih-Chun Gan, Shi-Rui Gupta, Deepak et al.

Source: Cerebellum. Apr2019, Vol. 18 Issue 2, p291-294. 4p.

Climbing fiber-Purkinje cell synaptic pathology across essential tremor subtypes.

Authors: Lee, Danielle Gan, Shi-Rui Faust, Phyllis L. et al.

Source: Parkinsonism & Related Disorders. Jun2018, Vol. 51, p24-29. 6p.

Dystonia and ataxia progression in spinocerebellar ataxias.

Authors: Kuo, Pei-Hsin Gan, Shi-Rui Wang, Jie et al.

Source: Parkinsonism & Related Disorders. Dec2017, Vol. 45, p75-80. 6p.

C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias.

Authors: Figueroa, Karla P. Gan, Shi‐Rui Perlman, Susan et al.

Source: Movement Disorders. Mar2018, Vol. 33 Issue 3, p497-498. 2p.

Intermittent Theta-Burst Stimulation (iTBS) Improves Motor Coordination and Modulates Neuroinflammation and Autophagy in SCA3/MJD Mice.

Authors: Chen, Le-Wen Lian, Yan-Hua Dong, Xiao-Lei et al.

Source: Cerebellum. Aug2026, Vol. 25 Issue 4, p1-15. 15p.

Associations between CAG repeat size, brain and spinal cord volume loss, and motor symptoms in spinocerebellar ataxia type 3: a cohort study.

Authors: Ye, Zhi-Xian Chen, Xuan-Yu Li, Meng-Cheng et al.

Source: Orphanet Journal of Rare Diseases. 1/23/2025, Vol. 20 Issue 1, p1-11. 11p.

A Novel Homozygous RRP12 Variant in a Chinese Patient with Early‐Onset Cerebellar Ataxia.

Authors: Lin, Wei Yuan, Ru‐Ying Zheng, Ze‐Hong et al.

Source: Movement Disorders. May2026, p1. 3p. 1 Illustration.

Correction to: Hispanic Spinocerebellar Ataxia Type 35 (SCA35) with a Novel Frameshift Mutation.

Authors: Lin, Chih-Chun Gan, Shi-Rui Gupta, Deepak et al.

Source: Cerebellum. 2021, Vol. 20 Issue 1, p140-140. 1p.

Peripheral inflammation in spinocerebellar ataxia type 3: associations with genetic and clinical manifestations.

Authors: Zhang, Jia-Yi Su, Qiu-Ni Lin, Han et al.

Source: Inflammation Research. 10/3/2025, Vol. 74 Issue 1, p1-10. 10p.

Altered brain white matter structural motor network in spinocerebellar ataxia type 3.

Authors: Chen, Xin‐Yuan Huang, Zi‐Qiang Lin, Wei et al.

Source: Annals of Clinical & Translational Neurology. Feb2023, Vol. 10 Issue 2, p225-236. 12p.

Static Posture Instability as a Sensitive Biomarker for Motor Abnormalities in Pre‐ataxic Spinocerebellar Ataxia Type 3 Patients.

Authors: Cui, Mao‐Lin Liu, Xia‐Hua Li, Ying et al.

Source: Movement Disorders. Apr2025, Vol. 40 Issue 4, p642-650. 9p.

Assessment of Peripheral Neuropathy Using Current Perception Threshold Measurement in Patients with Spinocerebellar Ataxia Type 3.

Authors: Liu, Xia-Hua Lin, Wei Xu, Hao-Ling et al.

Source: Cerebellum. Apr2025, Vol. 24 Issue 2, p1-8. 8p.

Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis.

Authors: Lu, Hai-Peng Gan, Shi-Rui Chen, Sheng et al.

Source: Neurobiology of Aging. Mar2015, Vol. 36 Issue 3, p1603.e11-1603.e14. 1p.