Detalhe da pesquisa
1.
Identifying clinical features and blood biomarkers associated with mild cognitive impairment in Parkinson disease using machine learning.
Eur J Neurol
; 30(6): 1658-1666, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36912424
2.
NOTCH2NLC GGC Repeat Expansions Are Associated with Sporadic Essential Tremor: Variable Disease Expressivity on Long-Term Follow-up.
Ann Neurol
; 88(3): 614-618, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32495371
3.
Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort.
Clin Genet
; 98(3): 274-281, 2020 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-32602554
4.
SNCA Rep1 promoter variability influences cognition in Parkinson's disease.
Mov Disord
; 34(8): 1232-1236, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31234238
5.
NOTCH2NLC-linked neuronal intranuclear inclusion body disease and fragile X-associated tremor/ataxia syndrome.
Brain
; 143(8): e69, 2020 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32789443
6.
Plasma Neurofilament Light Relates to Divergent Default and Salience Network Connectivity in Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia.
J Alzheimers Dis
; 2024 May 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38759005
7.
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese Ancestry.
J Mov Disord
; 17(2): 213-217, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38291878
8.
Higher serum triglyceride levels are associated with Parkinson's disease mild cognitive impairment.
Mov Disord
; 33(12): 1970-1971, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30345542
9.
Plasma Soluble ST2 Levels Are Higher in Neurodegenerative Disorders and Associated with Poorer Cognition.
J Alzheimers Dis
; 92(2): 573-580, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36776067
10.
Unique Clinical, Radiological and Histopathological Characteristics of a Southeast Asian Cohort of Patients with Limb-Girdle Muscular Dystrophy 2G/LGMD-R7-Telethonin-Related.
J Neuromuscul Dis
; 10(1): 91-106, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36463458
11.
C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort.
Ann Clin Transl Neurol
; 10(4): 568-578, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36799407
12.
New insights from a multi-ethnic Asian progressive supranuclear palsy cohort.
Parkinsonism Relat Disord
; 108: 105296, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36682278
13.
APOE4 and Confluent White Matter Hyperintensities Have a Synergistic Effect on Episodic Memory Impairment in Prodromal Dementia.
J Alzheimers Dis
; 87(3): 1103-1114, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35431245
14.
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPH.
Front Neurol
; 13: 868000, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35903111
15.
Upregulated Blood miR-150-5p in Alzheimer's Disease Dementia Is Associated with Cognition, Cerebrospinal Fluid Amyloid-ß, and Cerebral Atrophy.
J Alzheimers Dis
; 88(4): 1567-1584, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35811521
16.
Biomarker characterization of clinical subtypes of Parkinson Disease.
NPJ Parkinsons Dis
; 8(1): 109, 2022 Aug 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-36038597
17.
Plasma Neurofilament Light Concentration Is Associated with Diffusion-Tensor MRI-Based Measures of Neurodegeneration in Early Parkinson's Disease.
J Parkinsons Dis
; 12(7): 2135-2146, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36057833
18.
Longitudinal Study of SNCA Rep1 Polymorphism on Executive Function in Early Parkinson's Disease.
J Parkinsons Dis
; 12(3): 865-870, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35068417
19.
Altered Cerebrospinal Fluid Exosomal microRNA Levels in Young-Onset Alzheimer's Disease and Frontotemporal Dementia.
J Alzheimers Dis Rep
; 5(1): 805-813, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34870106
20.
High Diagnostic Utility Incorporating a Targeted Neurodegeneration Gene Panel With MRI Brain Diagnostic Algorithms in Patients With Young-Onset Cognitive Impairment With Leukodystrophy.
Front Neurol
; 12: 631407, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33597917