首页 文献索引 SCI期刊 AI助手
期刊目录筛选

期刊名:Arquivos de neuro-psiquiatria

缩写:ARQ NEURO-PSIQUIAT

ISSN:0004-282X

e-ISSN:1678-4227

IF/分区:1.9/Q3

文章目录 更多期刊信息

共收录本刊相关文章索引3693
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Juan Sebastián Sánchez-León,Alexandre Baldissera,Giovana Zazo Guidio et al. Juan Sebastián Sánchez-León et al.
Background: Deep brain stimulation (DBS) is an established surgical therapy for advanced Parkinson's disease (PD), but, in Latin America, access remains restricted, and local data are limited. ...
Danilo Assis Pereira,Flávia Mariana Borges Montalvão Marques,Isabella Allegretti et al. Danilo Assis Pereira et al.
Background: Caring for children with infantile neuroaxonal dystrophy (INAD), a rare and progressive degenerative disease, can compromise mental health and consequently affect the quality of care given; however, there are ...
Xiaoguang Lang,Nuan Yang,Linxi Li et al. Xiaoguang Lang et al.
Background: The use of electroacupuncture can regulate brain activity, facilitating consciousness recovery. Objective: To investigate t...
Hüseyin Yiğit,Abdulkerim Gökoğlu Hüseyin Yiğit
Background: Dystonia is a large-scale motor network disorder involving the basal ganglia, cerebellum, and thalamus. Objective: This stu...
Kübra Mehel Metin,Selda Keskin Güler,Sinan Yetkin et al. Kübra Mehel Metin et al.
Background: Exploding head syndrome (EHS) is defined by the sudden onset of a short-term loud sounds or explosion-like sensation in the head during sleep, or sleep-wake transitions. ...
Matheus de Lima Ruffini,Danilo de Assis Pereira,Rafael Saliba Helmer et al. Matheus de Lima Ruffini et al.
Background: Leukodystrophies are inherited disorders that primarily affect the central nervous system white matter and often present with nonspecific symptoms, making early diagnosis difficult. Magnetic resonance imaging ...
Vanessa Van Der Linden,Alessandra Paula de Melo Calado,Gabriela Van Der Linden et al. Vanessa Van Der Linden et al.
Background: Spinal muscular atrophy (SMA) is a progressive, autosomal recessive motor neuron disorder caused by mutations in the SMN1 gene. While clinical trials in type-I and -II SMA led to the approval of nusinersen for...