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Livia Bernardi

University of Florence
H指数:24
被引数:2,357

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Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor

卡拉布里亚阿尔茨海默病患者的淀粉样前体蛋白A713T突变: 一种估计共同祖先遗传的群体基因组学方法

2021-12-2314
OAAI
Genetic variation in APOE, GRN, and TP53 are phenotype modifiers in frontotemporal dementia

APOE,GRN和TP53的遗传变异是额颞叶痴呆的表型修饰因子

2021-03-017
OAAI
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

C9orf72,发病年龄和祖先有助于区分FTLD队列中的行为和语言变体

2020-12-158
OAAI
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease

ATXN1,ATXN2和HTT中间重复序列在额颞叶痴呆和阿尔茨海默病中的作用

2020-03-0132
OAAI
Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
2019-07-269
OAAI
Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia

介导神经退行性痴呆的进化保守基因网络的鉴定

2018-12-0398
OAAI
Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia

卡拉布里亚人群中心血管遗传危险因素的频率及其对痴呆的影响

2018-01-095
PREAI
The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family
2017-08-0117
PREAI
Role of Niemann-Pick Type C Disease Mutations in Dementia
2016-12-0625
PREAI
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia
2015-10-0151
OAAI
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
2015-06-0230
OAAI
Identification of Three Novel LRRK2 Mutations associated with Parkinson's Disease in a Calabrian Population

在卡拉布里亚人群中鉴定与帕金森病相关的三种新型LRRK2突变

2013-11-136
PREAI
Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in Southern Italy
2012-12-0135
OAAI