Lista de obras - Claudio Bruno Mariani - Dominio Público Uruguay

A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease

artículo científico publicado en 2006

A novel study and meta-analysis of the genetic variation of the serotonin transporter promoter in the italian population do not support a large effect on Alzheimer's disease risk

artículo científico publicado en 2011

Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration

artículo científico publicado en 2006

Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.

artículo científico publicado en 2005

Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy

artículo científico publicado en 2008

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

artículo científico publicado en 2013

BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

scientific article published on 01 January 2011

Body Mass Index Predicts Progression of Mild Cognitive Impairment to Dementia.

artículo científico publicado en 2016

CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2009

CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's disease

artículo científico publicado en 2004

Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease

article

Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease.

artículo científico publicado en 2010

Does Vascular Burden Contribute to the Progression of Mild Cognitive Impairment to Dementia?

artículo científico publicado en 2012

Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease.

artículo científico publicado en 2013

FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration

scientific article published on 01 January 2010

GRN variability contributes to sporadic frontotemporal lobar degeneration

artículo científico publicado en 2010

Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2012

Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients

artículo científico publicado en 2005

Interaction between the APOE epsilon4 allele and the APH-1b c + 651T > G SNP in Alzheimer's disease.

artículo científico publicado en 2007

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

artículo científico publicado en 2010

MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels

artículo científico publicado en 2009

MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.

artículo científico publicado en 2004

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis

artículo científico publicado en 2005

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

artículo científico publicado en 2016

Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.

artículo científico publicado en 2013

Physical activity reduces the risk of dementia in mild cognitive impairment subjects: a cohort study

artículo científico publicado en 2014

Plasma levels of beta-amyloid (1-42) in Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2006

Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer disease

artículo científico publicado en 2011

Replication study to confirm the role of CYP2D6 polymorphism rs1080985 on donepezil efficacy in Alzheimer's disease patients.

artículo científico publicado en 2012

Reversible Mild Cognitive Impairment: The Role of Comorbidities at Baseline Evaluation.

artículo científico publicado en 2016

Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis.

artículo científico publicado en 2011

Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.

artículo científico publicado en 2011

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

artículo científico publicado en 2009

Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in Italy

artículo científico publicado en 2009

Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease

artículo científico publicado en 2005

Serum folate concentrations in patients with cortical and subcortical dementias

artículo científico publicado en 2007

The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts.

artículo científico publicado en 2012

The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression.

artículo científico publicado en 2005

The serotonin transporter promoter polymorphic region is not a risk factor for Alzheimer's disease related behavioral disturbances.

artículo científico publicado en 2009

Transmembrane protein 106B gene (TMEM106B) variability and influence on progranulin plasma levels in patients with Alzheimer's disease.

artículo científico publicado en 2015

Weight Loss Predicts Progression of Mild Cognitive Impairment to Alzheimer's Disease.

artículo científico publicado en 2016

Lista de obras de Claudio Bruno Mariani

A novel polymorphism in SEL1L confers susceptibility to Alzheimer's disease

A novel study and meta-analysis of the genetic variation of the serotonin transporter promoter in the italian population do not support a large effect on Alzheimer's disease risk

Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration

Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.

Association study to evaluate the serotonin transporter and apolipoprotein E genes in frontotemporal lobar degeneration in Italy

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

BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease

Body Mass Index Predicts Progression of Mild Cognitive Impairment to Dementia.

CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration

CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's disease

Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease

Cell-dependent kinase inhibitor 2A and 2B genetic variability in patients with Alzheimer's disease.

Does Vascular Burden Contribute to the Progression of Mild Cognitive Impairment to Dementia?

Expression of the transcription factor Sp1 and its regulatory hsa-miR-29b in peripheral blood mononuclear cells from patients with Alzheimer's disease.

FUS/TLS Genetic Variability in Sporadic Frontotemporal Lobar Degeneration

GRN variability contributes to sporadic frontotemporal lobar degeneration

Genetics and expression analysis of the specificity protein 4 gene (SP4) in patients with Alzheimer's disease and frontotemporal lobar degeneration

Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients

Interaction between the APOE epsilon4 allele and the APH-1b c + 651T > G SNP in Alzheimer's disease.

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels

MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.

Physical activity reduces the risk of dementia in mild cognitive impairment subjects: a cohort study

Plasma levels of beta-amyloid (1-42) in Alzheimer's disease and mild cognitive impairment

Position paper of the Italian Society for the study of Dementias (SINDEM) on the proposal of a new lexicon on Alzheimer disease

Replication study to confirm the role of CYP2D6 polymorphism rs1080985 on donepezil efficacy in Alzheimer's disease patients.

Reversible Mild Cognitive Impairment: The Role of Comorbidities at Baseline Evaluation.

Role of OLR1 and its regulating hsa-miR369-3p in Alzheimer's disease: genetics and expression analysis.

Role of hnRNP-A1 and miR-590-3p in neuronal death: genetics and expression analysis in patients with Alzheimer disease and frontotemporal lobar degeneration.

Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease

Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in Italy

Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease

Serum folate concentrations in patients with cortical and subcortical dementias

The SIRT2 polymorphism rs10410544 and risk of Alzheimer's disease in two Caucasian case-control cohorts.

The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression.

The serotonin transporter promoter polymorphic region is not a risk factor for Alzheimer's disease related behavioral disturbances.

Transmembrane protein 106B gene (TMEM106B) variability and influence on progranulin plasma levels in patients with Alzheimer's disease.

Weight Loss Predicts Progression of Mild Cognitive Impairment to Alzheimer's Disease.