Detalhe da pesquisa
1.
Transcriptomic profiling and regulatory pathways of cardiac resident macrophages in aging.
Cell Mol Life Sci
; 81(1): 220, 2024 May 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38763956
2.
Atypical and delayed spinal cord MRI features of COVID-19-associated myelopathies: a report of four cases and literature review.
Neurol Sci
; 45(5): 1835-1843, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38430399
3.
5' UTR CGG repeat expansion in GIPC1 is associated with oculopharyngodistal myopathy.
Brain
; 144(2): 601-614, 2021 03 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33374016
4.
The non-syndromic clinical spectrums of mtDNA 3243A>G mutation.
Neurosciences (Riyadh)
; 26(2): 128-133, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33814365
5.
Prevalence and Risk Factors of White Matter Lesions in Tibetan Patients Without Acute Stroke.
Stroke
; 51(1): 149-153, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31679502
6.
Characteristics of acute ischemic stroke in hospitalized patients in Tibet: a retrospective comparative study.
BMC Neurol
; 20(1): 380, 2020 Oct 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33087079
7.
Acute mitochondrial myopathy with respiratory insufficiency and motor axonal polyneuropathy.
Int J Neurosci
; 128(3): 231-236, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28969510
8.
Adenylyl cyclase 6 activation negatively regulates TLR4 signaling through lipid raft-mediated endocytosis.
J Immunol
; 191(12): 6093-100, 2013 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24218452
9.
Association between high-resolution magnetic resonance vessel wall imaging characteristics and recurrent stroke in patients with intracranial atherosclerotic steno-occlusive disease: A prospective multicenter study.
Int J Stroke
; 19(5): 569-576, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38229443
10.
Two patients with congenital myasthenic syndrome caused by COLQ gene mutations and the consequent ColQ protein defect.
Heliyon
; 9(2): e13272, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36798769
11.
Factors Associated With Alzheimer's Disease Patients' Caregiving Status and Family Caregiving Burden in China.
Front Aging Neurosci
; 14: 865933, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35370609
12.
Differences in treatment for Alzheimer's disease between urban and rural areas in China.
Front Neurol
; 13: 996093, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36247753
13.
Retinitis pigmentosa and molar tooth sign caused by novel AHI1 compound heterozygote pathogenic variants.
BMC Med Genomics
; 14(1): 242, 2021 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34627237
14.
The Association between Neprilysin gene polymorphisms and Alzheimer's disease in Tibetan population.
Brain Behav
; 11(3): e02002, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33314757
15.
Anti-inflammatory effects of α7-nicotinic ACh receptors are exerted through interactions with adenylyl cyclase-6.
Br J Pharmacol
; 178(11): 2324-2338, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33598912
16.
Heteroplasmy and phenotype spectrum of the mitochondrial tRNALeu (UUR) gene m.3243A>G mutation in seven Han Chinese families.
J Neurol Sci
; 408: 116562, 2020 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31722256
17.
Design of stroke imaging package study of intracranial atherosclerosis: a multicenter, prospective, cohort study.
Ann Transl Med
; 8(1): 13, 2020 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32055604
18.
A novel Twinkle (PEO1) gene mutation in a Chinese family with adPEO.
Mol Vis
; 14: 1995-2001, 2008.
Artigo
em Inglês
| MEDLINE | ID: mdl-18989381
19.
Deep Brain Stimulation: A Potential Treatment for Dementia in Alzheimer's Disease (AD) and Parkinson's Disease Dementia (PDD).
Front Neurosci
; 12: 360, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29896085
20.
MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load.
EBioMedicine
; 30: 86-93, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29506874