A New Phenotype of TUBB4A Mutation in a Family With Adult-Onset Progressive Spastic Paraplegia and Isolated Hypomyelination Leukodystrophy: A Case Report and Literature Review.
A fixel-based analysis of white matter reductions early detects Parkinson disease with mild cognitive impairment.
Novel Compound Heterozygous Mutations in the SYNE1 Gene in a Taiwanese Family: A Case Report and Literature Review.
Phosphorylated α-synuclein in diluted human serum as a biomarker for Parkinson's disease.
UQCRC1 variants in early-onset and familial Parkinson's disease in a Taiwanese cohort.
Diagnosis and Clinical Features in Autoimmune-Mediated Movement Disorders.
Association of ITPKB, IL1R2 and COQ7 with Parkinson's disease in Taiwan.
Association of AXIN1 With Parkinson's Disease in a Taiwanese Population.
Fixel-Based Analysis Effectively Identifies White Matter Tract Degeneration in Huntington's Disease.
Fibroblast Growth Factor 20 Gene Polymorphism in Parkinson's Disease in Asian Population: A Meta-Analysis.
Role of LRP10 in Parkinson's disease in a Taiwanese cohort.
Reappraisal of the incidence, various types and risk factors of malignancies in patients with dermatomyositis and polymyositis in Taiwan.
"Hot cross bun" is a potential imaging marker for the severity of cerebellar ataxia in MSA-C.
Pathomechanism Characterization and Potential Therapeutics Identification for Parkinson's Disease Targeting Neuroinflammation.
Association of SOD2 p.V16A polymorphism with Parkinson's disease: A meta-analysis in Han Chinese.
Pathomechanism characterization and potential therapeutics identification for SCA3 targeting neuroinflammation.
Rare VPS35 A320V Variant in Taiwanese Parkinson's Disease Indicates Disrupted CI-MPR Sorting and Impaired Mitochondrial Morphology.
Serum levels of cell adhesion molecules in patients with neuromyelitis optica spectrum disorder.
Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.
Lactulose and Melibiose Attenuate MPTP-Induced Parkinson's Disease in Mice by Inhibition of Oxidative Stress, Reduction of Neuroinflammation and Up-Regulation of Autophagy.
Exploration of multi-target effects of 3-benzoyl-5-hydroxychromen-2-one in Alzheimer's disease cell and mouse models.
Lactulose and Melibiose Inhibit α-Synuclein Aggregation and Up-Regulate Autophagy to Reduce Neuronal Vulnerability.
Variants in saposin D domain of prosaposin gene linked to Parkinson's disease.
New Synthetic 3-Benzoyl-5-Hydroxy-2 H-Chromen-2-One (LM-031) Inhibits Polyglutamine Aggregation and Promotes Neurite Outgrowth through Enhancement of CREB, NRF2, and Reduction of AMPK α in SCA17 Cell Models.
Genetic Analysis of EGLN1 C127S Variant in Taiwanese Parkinson's Disease.
Association of genetic variants within HLA-DR region with Parkinson's disease in Taiwan.
Association of RIT2 and RAB7L1 with Parkinson's disease: a case-control study in a Taiwanese cohort and a meta-analysis in Asian populations.
Delivering patient-centered care in Parkinson's disease: Challenges and consensus from an international panel.
Plasma and Serum Alpha-Synuclein as a Biomarker of Diagnosis in Patients With Parkinson's Disease.
Does the M.D. Anderson Dysphagia Inventory correlate with dysphagia-limit and the Unified Parkinson Disease Rating Scale in early-stage Parkinson's disease?
Neuroprotection of Indole-Derivative Compound NC001-8 by the Regulation of the NRF2 Pathway in Parkinson's Disease Cell Models.
Acupuncture Effect and Mechanism for Treating Pain in Patients With Parkinson's Disease.
Association between CSF1 and CSF1R Polymorphisms and Parkinson's Disease in Taiwan.
CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan.
Parkinson's disease in the Western Pacific Region.
Using global team science to identify genetic parkinson's disease worldwide.
Galectin-3 is required for the microglia-mediated brain inflammation in a model of Huntington's disease.
POLG R964C and GBA L444P mutations in familial Parkinson's disease: Case report and literature review.
Anxiety and Levodopa Equivalent Daily Dose Are Potential Predictors of Sleep Quality in Patients With Parkinson Disease in Taiwan.
Shaoyao Gancao Tang (SG-Tang), a formulated Chinese medicine, reduces aggregation and exerts neuroprotection in spinocerebellar ataxia type 17 (SCA17) cell and mouse models.
Targeting Ubiquitin Proteasome Pathway with Traditional Chinese Medicine for Treatment of Spinocerebellar Ataxia Type 3.
Polymorphisms of ACMSD-TMEM163, MCCC1, and BCKDK-STX1B Are Not Associated with Parkinson's Disease in Taiwan.
Formulated Chinese Medicine Shaoyao Gancao Tang Reduces Tau Aggregation and Exerts Neuroprotection through Anti-Oxidation and Anti-Inflammation.
Home-Based Orolingual Exercise Improves the Coordination of Swallowing and Respiration in Early Parkinson Disease: A Quasi-Experimental Before-and-After Exercise Program Study.
Alternations of Metabolic Profile and Kynurenine Metabolism in the Plasma of Parkinson's Disease.
Predictive Factors for Early Initiation of Artificial Feeding in Patients With Sporadic Creutzfeldt-Jakob Disease.
Analysis of GWAS-linked variants in multiple system atrophy.
The indole compound NC009-1 inhibits aggregation and promotes neurite outgrowth through enhancement of HSPB1 in SCA17 cells and ameliorates the behavioral deficits in SCA17 mice.
Genetic and functional characters of GRN p.T487I mutation in Taiwanese patients with atypical parkinsonian disorders.
Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease.
DLG2, but not TMEM229B, GPNMB, and ITGA8 polymorphism, is associated with Parkinson's disease in a Taiwanese population.
Atypical presentation of dopa-responsive dystonia in Taiwan.
Elevated serum levels of endothelin-1 in patients with chronic inflammatory demyelinating polyneuropathy.
Down-regulation of miR-9* in the peripheral leukocytes of Huntington's disease patients.
Altered Aconitase 2 Activity in Huntington's Disease Peripheral Blood Cells and Mouse Model Striatum.
Non-invasive assessment determine the swallowing and respiration dysfunction in early Parkinson's disease.
Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease.
Cross-Cultural Differences of the Non-Motor Symptoms Studied by the Traditional Chinese Version of the International Parkinson and Movement Disorder Society- Unified Parkinson's Disease Rating Scale.
Patterns of False Memory in Patients with Huntington's Disease.
Targeting ENT1 and adenosine tone for the treatment of Huntington's disease.
Genome-wide association study of Parkinson's disease in East Asians.
Medicinal herbs Oenanthe javanica (Blume) DC., Casuarina equisetifolia L. and Sorghum bicolor (L.) Moench protect human cells from MPP+ damage via inducing FBXO7 expression.
Positive Effects of Specific Exercise and Novel Turning-based Treadmill Training on Turning Performance in Individuals with Parkinson's disease: A Randomized Controlled Trial.
Increased serum concentrations of transforming growth factor-β1 (TGF-β1) in patients with Guillain-Barre syndrome.
The Potential of Indole/Indolylquinoline Compounds in Tau Misfolding Reduction by Enhancement of HSPB1.
Relationships among Depression, Anxiety, Sleep, and Quality of Life in Patients with Parkinson's Disease in Taiwan.
Functional properties of LRRK2 mutations in Taiwanese Parkinson disease.
Identifying GSK-3β kinase inhibitors of Alzheimer's disease: Virtual screening, enzyme, and cell assays.
Metabolic disturbances in plasma as biomarkers for Huntington's disease.
The aqueous extract of Glycyrrhiza inflata can upregulate unfolded protein response-mediated chaperones to reduce tau misfolding in cell models of Alzheimer's disease.
Associations of Matrix Metalloproteinase-9 and Tissue Inhibitory Factor-1 Polymorphisms With Parkinson Disease in Taiwan.
Association of GCH1 and MIR4697, but not SIPA1L2 and VPS13C polymorphisms, with Parkinson's disease in Taiwan.
Impairment of proteasome and anti-oxidative pathways in the induced pluripotent stem cell model for sporadic Parkinson's disease.
Memory for gist and detail information in patients with Parkinson's disease.
Eukaryotic translation initiation factor 4-γ, 1 gene mutations are rare in Parkinson's disease among Taiwanese.
STK39, But Not BST1, HLA-DQB1, and SPPL2B Polymorphism, Is Associated With Han-Chinese Parkinson's Disease in Taiwan.
Novel Lactulose and Melibiose Targeting Autophagy to Reduce PolyQ Aggregation in Cell Models of Spinocerebellar Ataxia 3.
Integrated non-invasive measurements reveal swallowing and respiration coordination recovery after unilateral stroke.
High Protein Diet and Huntington's Disease.
Protein Kinase Cη Polymorphism and the Susceptibility to Ischemic Stroke in the Taiwan Population.
The potential of lactulose and melibiose, two novel trehalase-indigestible and autophagy-inducing disaccharides, for polyQ-mediated neurodegenerative disease treatment.
Wegener's granulomatosis with nervous system involvement: a hospital-based study.
Clinical and radiological findings suggesting disorders other than tolosa-hunt syndrome among ophthalmoplegic patients: a retrospective analysis.
Virtual Reality-Based Training to Improve Obstacle-Crossing Performance and Dynamic Balance in Patients With Parkinson's Disease.
Comparison between the cranial magnetic resonance imaging features of neuromyelitis optica spectrum disorder versus multiple sclerosis in Taiwanese patients.
Clinical correlations of motor and somatosensory evoked potentials in neuromyelitis optica.
High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia.
Plasma inflammatory biomarkers for Huntington's disease patients and mouse model.
The potential of indole and a synthetic derivative for polyQ aggregation reduction by enhancement of the chaperone and autophagy systems.
Taiwan Severe Cutaneous Adverse Reaction Consortium; Japan Pharmacogenomics Data Science Consortium. Genetic variants associated with phenytoin-related severe cutaneous adverse reactions.
FBXO7 Y52C Polymorphism as a Potential Protective Factor in Parkinson's Disease.
Structural study of the microtubule-associated protein tau locus of Alzheimer's disease in Taiwan.
Tract-based spatial statistics: application to mild cognitive impairment.
Factors influencing turning and its relationship with falls in individuals with Parkinson's disease.
Inhibition of soluble tumor necrosis factor is therapeutic in Huntington's disease.
Aqueous extract of Glycyrrhiza inflata inhibits aggregation by upregulating PPARGC1A and NFE2L2-ARE pathways in cell models of spinocerebellar ataxia 3.
Variant R244H in Na+/Mg2+ exchanger SLC41A1 in Taiwanese Parkinson's disease is associated with loss of Mg2+ efflux function. Parkinsonism Relat Disord.
Factors influencing obstacle crossing performance in patients with Parkinson's disease.
Aqueous extract of Gardenia jasminoides targeting oxidative stress to reduce polyQ aggregation in cell models of spinocerebellar ataxia 3.
Downregulation of proteins involved in the endoplasmic reticulum stress response and Nrf2-ARE signaling in lymphoblastoid cells of spinocerebellar ataxia type 17.
Genetic Variants ofLRRK2 in Taiwanese Parkinson's Disease.
HTRA2 variations in Taiwanese Parkinson's disease.
Sex dimorphism of cortical water diffusion in normal aging measured by magnetic resonance imaging.
The experiences of taiwanese older individuals at different stages of Parkinson disease.
Internal Ribosome Entry Segment Activity of ATXN8 Opposite Strand RNA.
SLC1A2 Variant Is Associated with Essential Tremor in Taiwanese Population.
Genetic variations of GAK in two Chinese Parkinson's disease populations: a case-control study.
Identification of a novel risk variant in the FUS gene in essential tremor.
Long-term follow-up of spinal and bulbar muscular atrophy in Taiwan.
Association between PARK16 and Parkinson's disease in the Han Chinese population: a meta-analysis.
Olfactory impairment and pathology in neurodegenerative disorders with brain iron accumulation.
Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population.
Aqueous Extract of Paeonia lactiflora and Paeoniflorin as Aggregation Reducers Targeting Chaperones in Cell Models of Spinocerebellar Ataxia 3.
Analyses of haptoglobin level in the cerebrospinal fluid and serum of patients with neuromyelitis optica and multiple sclerosis.
A comparison of benign and inflammatory manifestations of Tolosa-Hunt syndrome.
Genetic analysis of NFE2L2 promoter variation in Taiwanese Parkinson's disease.
Downregulation of genes involved in metabolism and oxidative stress in the peripheral leukocytes of Huntington's disease patients.
Protein kinase Cη polymorphism and the susceptibilities to intracerebral hemorrhage in the Taiwan population.
Distinct features between longitudinally extensive transverse myelitis presenting with and without anti-Aquaporin 4 antibodies.
LRRK2 A419V Is Not Associated with Parkinson's Disease in Different Chinese Populations.
Effect of statin treatment on adrenomyeloneuropathy with cerebral inflammation: A revisit.
ATXN8 -62 G/A promoter polymorphism and risk of Taiwanese Parkinson's disease.
Genetic analysis of HLA-DRA region variation in Taiwanese Parkinson's disease.
Identification of gene networks and pathways associated with guillain-barre syndrome.
LINGO-2 polymorphism and risk of Parkinson's disease in Taiwan.
Are there ethnic differences in Impulsive/Compulsive behaviors in Parkinson's disease?
