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期刊名:Brain and nerve

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ISSN:1881-6096

e-ISSN:1344-8129

IF/分区:0.0/

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共收录本刊相关文章索引2832
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
Nanami Yamanaka,Masaya Honda,So Kanda et al. Nanami Yamanaka et al.
A 50year-old female was diagnosed with myasthenia gravis (MG) following aspiration pneumonia. Despite treatment with prednisolone (5mg/day) and intravenous immunoglobulin (IVIg), the bulbar palsy persisted. Additionally, chest CT revealed f...
Shoichiro Sato,Atsushi Iwata,Kenji Ishii et al. Shoichiro Sato et al.
Alzheimer's disease is an age-related neurodegenerative disorder, and is considered to contribute to dementia in 60%-70% of individuals with dementia. In recent years, a series of amyloid β protein (Aβ)-targeting antibodies that act direc...
Mayu Takahashi Mayu Takahashi
This article deals with the neural circuits involved in the generation and suppression of saccadic eye movements. Voluntary eye movements are known to be organized in two-dimensional horizontal and vertical coordinate system, whereas the ve...
Shun Kudo Shun Kudo
"Aphantasia" refers to the inability to create voluntary mental images. Most studies have assessed aphantasia using questionnaires; however, recently, there have been attempts to quantify aphantasia using objective measures such as pupillar...
Takashi Kurashige Takashi Kurashige
Sporadic late-onset nemaline myopathy (SLONM) is distinct from congenital nemaline myopathies, which are associated with genetic abnormalities. There are many cases of SLONM with M-proteinemia, but treatment response and life expectancy are...
Michiaki Koga Michiaki Koga
M-protein and neuropathy are highly prevalent and often coincide without causal relationships. However, some M-proteins induce neuropathies, which are diverse and require a multifaceted approach to investigate M protein characteristics, neu...
Ryota Sato,Takashi Kanda Ryota Sato
Anti-myelin-associated glycoprotein neuropathy is now recognized as a distinct clinicopathological entity. Since its initial description over 40 years ago, substantial advances have been made in elucidating its pathogenic mechanisms, standa...
Tomoki Suichi,Sonoko Misawa Tomoki Suichi
POEMS syndrome is a systemic disease characterized by monoclonal plasma cell proliferation and the overproduction of the vascular endothelial growth factor. Japanese researchers have made significant contributions to the establishment of di...
Toshihiro Ide,Haruki Koike Toshihiro Ide
AL amyloidosis is a systemic disease caused by misfolded immunoglobulin light chains deposited as amyloid fibrils in multiple organs. Peripheral neuropathy, which often presents with sensory dissociation and autonomic dysfunction, is a key ...
Takamitsu Watanabe Takamitsu Watanabe
Autism spectrum disorder is characterized by socio-communicative traits and cognitive inflexibility. Here, we present a series of findings indicating that autistic neural rigidity is a key neural mechanism underpinning for both social and n...