Detalhe da pesquisa
1.
Comparison of endoscopic third ventriculostomy versus cerebrospinal fluid shunt procedures for the treatment of pediatric hydrocephalus in Taiwan.
Childs Nerv Syst
; 2024 May 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38806857
2.
EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.
Ann Neurol
; 89(3): 485-497, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33236446
3.
Pparα deficiency inhibits the proliferation of neuronal and glial precursors in the zebrafish central nervous system.
Dev Dyn
; 247(12): 1264-1275, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30358936
4.
Regulator of G protein signaling 2 (Rgs2) regulates neural crest development through Pparδ-Sox10 cascade.
Biochim Biophys Acta Mol Cell Res
; 1864(3): 463-474, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27979767
5.
Genetic diagnosis of neurofibromatosis type 1: targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis.
J Biomed Sci
; 25(1): 72, 2018 Oct 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30290804
6.
Adult PHACE Syndrome Presenting With Visual Field Loss: A Case Report and Review of the Literature.
J Neuroophthalmol
; 2023 Apr 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-37078913
7.
Neurofibromatosis-1 regulates neuroglial progenitor proliferation and glial differentiation in a brain region-specific manner.
Genes Dev
; 24(20): 2317-29, 2010 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20876733
8.
The transcription factor hairy/E(spl)-related 2 induces proliferation of neural progenitors and regulates neurogenesis and gliogenesis.
Dev Biol
; 397(1): 116-28, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25446033
9.
Paroxysmal exercise-induced dystonia within the phenotypic spectrum of ECHS1 deficiency.
Mov Disord
; 31(7): 1041-8, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27090768
10.
XLID CUL4B mutants are defective in promoting TSC2 degradation and positively regulating mTOR signaling in neocortical neurons.
Biochim Biophys Acta
; 1832(4): 585-93, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23348097
11.
(G2019S) LRRK2 causes early-phase dysfunction of SNpc dopaminergic neurons and impairment of corticostriatal long-term depression in the PD transgenic mouse.
Neurobiol Dis
; 68: 190-9, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24830390
12.
10 weeks low intensity treadmill exercise intervention ameliorates motor deficits and sustains muscle mass via decreasing oxidative damage and increasing mitochondria function in a rat model of Parkinson's disease.
Life Sci
; 350: 122733, 2024 May 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38763432
13.
Dystonic opisthotonus: a "red flag" for neurodegeneration with brain iron accumulation syndromes?
Mov Disord
; 28(10): 1325-9, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23736975
14.
Phenotypes and genotypes of patients with pantothenate kinase-associated neurodegeneration in Asian and Caucasian populations: 2 cases and literature review.
ScientificWorldJournal
; 2013: 860539, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24348190
15.
Etv5a Suppresses Neural Progenitor Cell Proliferation by Inhibiting sox2 Transcription.
Stem Cells Dev
; 32(17-18): 524-538, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37358404
16.
Deficiency of RAB39B Activates ER Stress-Induced Pro-apoptotic Pathway and Causes Mitochondrial Dysfunction and Oxidative Stress in Dopaminergic Neurons by Impairing Autophagy and Upregulating α-Synuclein.
Mol Neurobiol
; 60(5): 2706-2728, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36715921
17.
HCH6-1, an antagonist of formyl peptide receptor-1, exerts anti-neuroinflammatory and neuroprotective effects in cellular and animal models of Parkinson's disease.
Biochem Pharmacol
; 212: 115524, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37001680
18.
PARK6 PINK1 mutants are defective in maintaining mitochondrial membrane potential and inhibiting ROS formation of substantia nigra dopaminergic neurons.
Biochim Biophys Acta
; 1812(6): 674-84, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21421046
19.
Mutations in TMEM230 are not a common cause of Parkinson's disease.
Mov Disord
; 32(2): 302-304, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28090676
20.
PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.
Am J Med Genet B Neuropsychiatr Genet
; 159B(2): 183-91, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22213678