arrow
S

Stéphanie Philtjens

VIB
H指数:12
被引数:2,048

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease
2021-02-1225
OAAI
Clinical variability and onset age modifiers in an extended Belgian GRN founder family
2018-07-0116
OAAI
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia

SORT1中罕见的非同义变异与额颞叶痴呆风险增加相关

2018-06-0122
OAAI
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
2015-12-15142
OAAI
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
2015-11-1014
OAAI
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia

研究罕见的杂合TREM2变体在阿尔茨海默病和额颞叶痴呆中的作用

2014-03-01182
OAAI