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Rosanna Colao

University of Florence
H指数:21
被引数:1,415

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Genetic variability in ADAM17/TACE is associated with sporadic Alzheimer's disease risk, neuropsychiatric symptoms and cognitive performance on the Rey Auditory Verbal Learning and Clock Drawing Tests

ADAM17/TACE的遗传变异与散发性阿尔茨海默病风险、神经精神症状以及Rey听觉言语学习测试和钟表绘制测试的认知表现相关。

2025-05-060
OA
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

全基因组分析揭示了MAPT,MOBP和APOE基因座在散发性额颞叶痴呆中的潜在作用

2024-07-010
OAAI
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
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
Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia

多个基因位点对额颞叶痴呆发病年龄的影响

2017-01-234
OAAI
Role of Niemann-Pick Type C Disease Mutations in Dementia
2016-12-0625
PREAI
Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol

阿尔茨海默氏病和额颞叶变性的遗传咨询和测试: 意大利共识协议

2016-02-2722
OAAI
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family
2015-06-0230
OAAI
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients
2015-02-26125
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