Lista de obras - Valentina Bessi - Dominio Público Uruguay

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

artículo científico publicado en 2013

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity

artículo científico publicado en 2006

Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer's disease: an 11-year follow-up study

scientific article published on 11 February 2020

Association analysis of the paraoxonase-1 gene with Alzheimer's disease

artículo científico publicado en 2006

Association of IL10 promoter polymorphism in Italian Alzheimer's disease

artículo científico publicado en 2007

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline

artículo científico publicado en 2017

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

artículo científico publicado en 2013

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

artículo científico publicado en 2021

Crossed aphasia confirmed by fMRI in a case with nonfluent variant of primary progressive aphasia carrying a GRN mutation

artículo científico publicado en 2019

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease

artículo científico publicado en 2010

Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

artículo científico publicado en 2011

Influence of ApoE Genotype and Clock T3111C Interaction with Cardiovascular Risk Factors on the Progression to Alzheimer's Disease in Subjective Cognitive Decline and Mild Cognitive Impairment Patients

scientific article published on 29 May 2020

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints

article

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease

artículo científico publicado en 2010

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

artículo científico publicado en 2014

PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment. A 10-year follow-up study

artículo científico publicado en 2020

Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and ApoE genotype

artículo científico publicado en 2007

Semantic dementia associated with mutation V363I in the tau gene

artículo científico publicado en 2010

Suitability of neuropsychological tests in patients with vascular dementia (VaD).

artículo científico publicado en 2012

TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients

artículo científico publicado en 2013

The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study

artículo científico publicado en 2019

Lista de obras de Valentina Bessi

A pan-European study of the C9orf72 repeat associated with FTLD: geographic prevalence, genomic instability, and intermediate repeats

Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity

Assessing the effectiveness of subjective cognitive decline plus criteria in predicting the progression to Alzheimer's disease: an 11-year follow-up study

Association analysis of the paraoxonase-1 gene with Alzheimer's disease

Association of IL10 promoter polymorphism in Italian Alzheimer's disease

Association of the New Variant Tyr424Asp at TBK1 Gene with Amyotrophic Lateral Sclerosis and Cognitive Decline

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

Crossed aphasia confirmed by fMRI in a case with nonfluent variant of primary progressive aphasia carrying a GRN mutation

Different implication of NEDD9 genetic variant in early and late-onset Alzheimer's disease

Implication of serotonin-transporter (5-HTT) gene polymorphism in subjective memory complaints and mild cognitive impairment (MCI).

Influence of ApoE Genotype and Clock T3111C Interaction with Cardiovascular Risk Factors on the Progression to Alzheimer's Disease in Subjective Cognitive Decline and Mild Cognitive Impairment Patients

KIBRA gene variants are associated with episodic memory performance in subjective memory complaints

Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment. A 10-year follow-up study

Pattern and progression of cognitive decline in Alzheimer's disease: role of premorbid intelligence and ApoE genotype

Semantic dementia associated with mutation V363I in the tau gene

Suitability of neuropsychological tests in patients with vascular dementia (VaD).

TOMM40 polymorphisms in Italian Alzheimer's disease and frontotemporal dementia patients

The implication of BDNF Val66Met polymorphism in progression from subjective cognitive decline to mild cognitive impairment and Alzheimer's disease: a 9-year follow-up study