「TDP-43 proteinopathyにおけるAtaxin-2の病理生化学的検討」の関連論文
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Multiple system atrophy variant with severe hippocampal pathology
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Assessment of amyloid deposition in patients with probable REM sleep behavior disorder as a prodromal symptom of dementia with Lewy bodies using PiB-PET
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Longitudinal Change of DAT SPECT in Parkinson's Disease and Multiple System Atrophy
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Semantic deficits in ALS related to right lingual/fusiform gyrus network involvement
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脳深部刺激療法施行下におけるパーキンソン病の病態解析研究
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Deep White Matter Lesions Are Associated with Early Recognition of Dementia in Alzheimer's Disease.
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Distinctive distribution of brain volume reductions in MELAS and mitochondrial DNA A3243G mutation carriers: A voxel-based morphometric study
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Lewy body disease primate model with α-synuclein propagation from the olfactory bulb
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The neural network basis of altered decision-making in patients with amyotrophic lateral sclerosis
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ジュベール症候群関連疾患の臨床遺伝学的解析
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脂肪酸結合タンパク質を介したシヌクレイノパチーの発症機序と治療薬に関する研究
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全エクソーム解析による成人発症遺伝性ミオパチーの新規遺伝子変異同定
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Pattern of THK 5351 retention in normal aging involves core regions of resting state networks associated with higher cognitive function
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Involvement of the Thalamus, Hippocampus, and Brainstem in Hypsarrhythmia of West Syndrome: Simultaneous Recordings of Electroencephalography and fMRI Study
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Structural abnormalities in nucleus accumbens in patients with panic disorder
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Can We Find Any Sustained Neurofunctional Alteration in Remitted Depressive Patients with a History of Modified Electroconvulsive Therapy?
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血管性認知障害におけるグリア細胞の病態生理学的役割の解明
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特発性正常圧水頭症におけるBlake’s pouch cyst様所見の検討
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Clinicopathological differences between the motor onset and psychiatric onset of Huntington’s disease, focusing on the nucleus accumbens
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PRKN遺伝子変異患者における分子遺伝学的多様性および神経病理学的特徴
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Association of orthostatic blood pressure with the symptoms of orthostatic hypotension and cognitive impairment in patients with multiple system atrophy
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Voxel-based morphometryを用いた有棘赤血球舞踏病とハンチントン病の比較検討および有棘赤血球舞踏病の画像所見と症状の経時的変化の評価
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小児MOG抗体関連疾患で見られる長期疼痛・感覚障害
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Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs
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Qualitative Deficits in Verbal Fluency in Parkinson’s Disease with Mild Cognitive Impairment: A Clinical and Neuroimaging Study
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病院総合診療医の診療対象になりうる新しい成人発症自己炎症性疾患 : VEXAS症候群
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Elevated serum creatine kinase in the early stage of sporadic amyotrophic lateral sclerosis
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Studies on the pathophysiology and current treatment status of ion channel-related muscle diseases
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Phosphorylated proteome analysis of a novel germline ABL1 mutation causing an autosomal dominant syndrome with ventricular septal defect
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Magnetic resonance-guided focused ultrasound thalamotomy restored distinctive resting-state networks in patients with essential tremor
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A heterozygous SERPINB7 mutation is a possible modifying factor for epidermolytic palmoplantar keratoderma
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アストロサイト活性化と神経変性に関連した ALS 複合バイオマーカーについての研究
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Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations
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Parkinson病における鏡像書字と発症機序
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Pseudo-sawtooth pattern on amplitude-integrated electroencephalography in neonatal hypoxic–ischemic encephalopathy
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医用画像を用いた骨粗鬆症とアルツハイマー病の連関―骨量減少に相関する脳領域の視覚化
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Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility
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The carboxyl-terminal region of SDCCAG8 comprises a functional module essential for cilia formation as well as organ development and homeostasis
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Whole-exome analysis of 177 pediatric patients with undiagnosed diseases
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Subjects at risk of Parkinson’s disease in health checkup examinees: cross-sectional analysis of baseline data of the NaT-PROBE study
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軽度認知障害患者の脳アミロイド沈着に対するフェルガード100Mの有効性
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Investigation of OLIG2 as a candidate gene for schizophrenia and autism spectrum disorder
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FLI1遺伝子マイクロサテライト多型と全身性強皮症との関連の検討
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忘れられない一枚の心電図 : カルモジュリン病
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Ependymoma-like tumors with mesenchymal differentiation harboring C11orf95-NCOA1/2 or -RELA fusion: a hitherto unclassified tumor related to ependymoma
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ADSSL1 myopathy is the most common nemaline myopathy in Japan with variable clinical features
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Neurogenic calf amyotrophy with CK elevation by entrapment radiculopathy; Clinical, radiological, and pathological analyses of 18 cases
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ADHD患者由来のiPS細胞から分化させた終脳オルガノイドでみられた大脳皮質の神経発生における変化
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悪性リンパ腫における血中循環細胞外遊離DNAを用いたゲノム解析に関する研究
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Impaired pain processing and its association with attention disturbance in patients with amyotrophic lateral sclerosis