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Akiyoshi Kakita

Niigata University
H指数:71
被引数:2.1万

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FTLD-TDP-43 With Motor Neuron Disease Pathology in an Autopsied Patient With Spastic Paraplegia-30B Harbouring a Homozygous KIF1A Variant

FTLD-TDP-43伴运动神经元病病理学表现:一例携带同源KIF1A变异的痉挛性截瘫-30B患者的尸检研究

2026-05-130
OAAI
Automated curation and museum archiving of large-scale tomography data for scientific research

自动化整理和博物馆归档大规模断层扫描数据以用于科学研究

2026-01-010
OA
Primary Brain Calcification: An International Consensus on Nomenclature, Diagnosis, Evaluation, and Management

原发性脑钙化:关于命名、诊断、评估和管理的国际共识

2025-12-010
PRE
Quantification of monoamine oxidase B expression with 11C-SL25.1188 for imaging reactive astrocytes in patients with Alzheimer’s disease

使用11C-SL25.1188对阿尔茨海默病患者中反应性星形胶质细胞中单胺氧化酶B的表达进行定量

2025-09-060
OAAI
Mosaic variants of neurodevelopmental and mitochondrial genes in postmortem paraventricular thalamus in bipolar disorder detected by deep exome sequencing

通过深度外显子测序检测到的双相障碍死后室旁丘脑中神经发育和线粒体基因的嵌合变异

2025-07-220
OAAI
Association of rare APOE missense variants with Alzheimer's disease in the Japanese population

日本人群中罕见APOE错义变异与阿尔茨海默病的相关性

2025-05-210
OA
Rapidly progressive scalp and lung metastases with fatal pneumothorax in glioblastoma, IDH-wildtype, with MET and CDK6 amplifications: a case report of clinical course and postmortem autopsy, including genetic analysis

快速进展的头皮和肺部转移伴致命性气胸的IDH-wildtype胶质母细胞瘤(伴有MET和CDK6扩增):一例临床病程及死后尸检的病例报告,包括遗传学分析

2025-05-200
PRE
Girdin deficiency causes developmental and epileptic encephalopathy with hippocampal sclerosis and interneuronopathy

Girdin缺乏会导致发育性和癫痫性脑病,并伴有海马硬化和中间神经病变

2024-12-150
OAAI