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

Association of fluvoxamine with mortality and symptom resolution among inpatients with COVID-19 in Uganda: a prospective interventional open-label cohort study

氟伏沙明与乌干达COVID-19住院患者死亡率和症状缓解的关系:一项前瞻性干预性开放标签队列研究

Kirenga, Bruce J; Mugenyi, Levicatus; Sánchez-Rico, Marina; Kyobe, Henry; Muttamba, Winters; Mugume, Raymond; Mwesigwa, Eliya; Kalimo, Ezra; Nyombi, Vicky; Segawa, Ivan; Namakula, Loryndah Olive; Sekibira, Rogers; Kabweru, Wilberforce; Byanyima, Rosemary; Aanyu, Hellen; Byakika-Kibwika, Pauline; Mwebesa, Henry G; Hoertel, Nicolas; Bazeyo, William

Severe elastolysis in hereditary gelsolin (AGel) amyloidosis

遗传性凝溶胶蛋白 (AGel) 淀粉样变性中的严重弹性蛋白溶解

Susanna Koskelainen, Fang Zhao, Hannu Kalimo, Marc Baumann, Sari Kiuru-Enari

Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL

血脑屏障渗漏并不是 CADASIL 白质病变的一致特征

Rikesh M Rajani, Julien Ratelade, Valérie Domenga-Denier, Yoshiki Hase, Hannu Kalimo, Raj N Kalaria, Anne Joutel

Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1

瑞典型多发性梗塞性痴呆是由COL4A1基因3'UTR突变引起的。

Siitonen, Maija; Börjesson-Hanson, Anne; Pöyhönen, Minna; Ora, Ari; Pasanen, Petra; Bras, Jose; Kern, Silke; Kern, Jürgen; Andersen, Oluf; Stanescu, Horia; Kleta, Robert; Baumann, Marc; Kalaria, Rajesh; Kalimo, Hannu; Singleton, Andy; Hardy, John; Viitanen, Matti; Myllykangas, Liisa; Guerreiro, Rita

Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases

丛集素/载脂蛋白 J 免疫反应与脑小血管病中的白质损伤有关

Lucinda Craggs, Julie Taylor, Janet Y Slade, Aiqing Chen, Christian Hagel, Gregor Kuhlenbaeumer, Anne Borjesson-Hanson, Matti Viitanen, Hannu Kalimo, Vincent Deramecourt, Arthur E Oakley, Raj N Kalaria

CADASIL and CARASIL

CADASI 和 CARASIL

Tikka, Saara; Baumann, Marc; Siitonen, Maija; Pasanen, Petra; Pöyhönen, Minna; Myllykangas, Liisa; Viitanen, Matti; Fukutake, Toshio; Cognat, Emmanuel; Joutel, Anne; Kalimo, Hannu

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

Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases.

定量血管病理学和家族性及散发性脑小血管疾病的表型分析

Craggs Lucinda J L, Hagel Christian, Kuhlenbaeumer Gregor, Borjesson-Hanson Anne, Andersen Oluf, Viitanen Matti, Kalimo Hannu, McLean Catriona A, Slade Janet Y, Hall Roslyn A, Oakley Arthur E, Yamamoto Yumi, Deramecourt Vincent, Kalaria Rajesh N

CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cells

CADASIL 突变和 NOTCH3 的 shRNA 沉默会影响培养的血管平滑肌细胞中的肌动蛋白组织。

Tikka, Saara; Ng, Yan Peng; Di Maio, Giuseppe; Mykkänen, Kati; Siitonen, Maija; Lepikhova, Tatiana; Pöyhönen, Minna; Viitanen, Matti; Virtanen, Ismo; Kalimo, Hannu; Baumann, Marc

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

新的突变巩固了 KCTD7 作为进行性肌阵挛性癫痫基因的地位

Maria Kousi, Verneri Anttila, Angela Schulz, Stella Calafato, Eveliina Jakkula, Erik Riesch, Liisa Myllykangas, Hannu Kalimo, Meral Topçu, Sarenur Gökben, Fusun Alehan, Johannes R Lemke, Michael Alber, Aarno Palotie, Outi Kopra, Anna-Elina Lehesjoki