日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ

北极 AβPP 突变导致阿尔茨海默病病理,表现为差异截短 Aβ 的高度可变拓扑沉积

Hannu Kalimo, Maciej Lalowski, Nenad Bogdanovic, Ola Philipson, Thomas D Bird, David Nochlin, Gerard D Schellenberg, Rosemarie Brundin, Tommie Olofsson, Rabah Soliymani, Marc Baumann, Oliver Wirths, Thomas A Bayer, Lars N G Nilsson, Hans Basun, Lars Lannfelt, Martin Ingelsson

Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotype

具有类似阿尔茨海默病tau蛋白病理和临床表型的家族性朊病毒病

Jayadev, Suman; Nochlin, David; Poorkaj, Parvoneh; Steinbart, Ellen J; Mastrianni, James A; Montine, Thomas J; Ghetti, Bernardino; Schellenberg, Gerard D; Bird, Thomas D; Leverenz, James B

Kikuchi-fujimoto disease associated with myasthenia gravis: a case report

菊池-藤本病合并重症肌无力:病例报告

Onasanya, Olukayode; Nochlin, David; Casas, Victor; Peddareddygari, Leema Reddy; Grewal, Raji P

Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease

北极APP基因突变导致早发性阿尔茨海默病的临床和神经病理学特征

Basun, Hans; Bogdanovic, Nenad; Ingelsson, Martin; Almkvist, Ove; Näslund, Jan; Axelman, Karin; Bird, Thomas D; Nochlin, David; Schellenberg, Gerard D; Wahlund, Lars-Olof; Lannfelt, Lars

Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease

三对患有家族性阿尔茨海默病的同卵双胞胎的临床病理一致性和不一致性

Brickell, Kiri L; Leverenz, James B; Steinbart, Ellen J; Rumbaugh, Malia; Schellenberg, Gerard D; Nochlin, David; Lampe, Thomas H; Holm, Ida E; Van Deerlin, Vivianna; Yuan, Wuxing; Bird, Thomas D

Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype

家族性阿尔茨海默病中的路易体病理:疾病和突变特异性病理表型的证据

Leverenz, James B; Fishel, Mark A; Peskind, Elaine R; Montine, Thomas J; Nochlin, David; Steinbart, Ellen; Raskind, Murray A; Schellenberg, Gerard D; Bird, Thomas D; Tsuang, Debby

Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2

19p13.2 染色体上存在一个新的晚发性阿尔茨海默病基因位点的证据

Wijsman, Ellen M; Daw, E Warwick; Yu, Change-En; Payami, Haydeh; Steinbart, Ellen J; Nochlin, David; Conlon, Erin M; Bird, Thomas D; Schellenberg, Gerard D

Effect of vascular lesions on cognition in Alzheimer's disease: a community-based study

血管病变对阿尔茨海默病患者认知功能的影响:一项基于社区的研究

Riekse, Robert G; Leverenz, James B; McCormick, Wayne; Bowen, James D; Teri, Linda; Nochlin, David; Simpson, Kate; Eugenio, Charisma; Larson, Eric B; Tsuang, Debby

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations

由A117V和F198S突变引起的格斯特曼-施特劳斯勒-沙因克氏病中,不同构象的朊病毒蛋白会积累。

Piccardo, P; Liepnieks, J J; William, A; Dlouhy, S R; Farlow, M R; Young, K; Nochlin, D; Bird, T D; Nixon, R R; Ball, M J; DeCarli, C; Bugiani, O; Tagliavini, F; Benson, M D; Ghetti, B

Transgenic mice over-expressing the C-99 fragment of betaPP with an alpha-secretase site mutation develop a myopathy similar to human inclusion body myositis

转基因小鼠过表达β-磷酸戊糖蛋白C-99片段,且该片段存在α-分泌酶位点突变,由此会产生类似于人类包涵体肌炎的肌病。

Jin, L W; Hearn, M G; Ogburn, C E; Dang, N; Nochlin, D; Ladiges, W C; Martin, G M