Lista de obras - Chiara Villa - Dominio Público Uruguay

A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

artículo científico publicado en 2011

Analysis of Human Papillomavirus (HPV) 16 Variants Associated with Cervical Infection in Italian Women

scientific article published on 01 January 2020

Arylsulfatase A (ASA) in Parkinson's Disease: From Pathogenesis to Biomarker Potential

artículo científico publicado en 2020

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

artículo científico publicado en 2013

Biomarkers for Alzheimer's Disease: Where Do We Stand and Where Are We Going?

artículo científico publicado en 2020

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

artículo científico publicado en 2013

C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

artículo científico publicado en 2013

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

artículo científico publicado en 2013

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

artículo científico publicado en 2009

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis

artículo científico publicado en 2007

Candidate gene analysis of selectin cluster in patients with multiple sclerosis

artículo científico publicado en 2009

Candidate gene analysis of semaphorins in patients with Alzheimer's disease

artículo científico publicado en 2009

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

artículo científico publicado en 2010

Circulating miRNAs as potential biomarkers in Alzheimer's disease

artículo científico publicado en 2014

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

artículo científico publicado en 2009

Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis

artículo científico publicado en 2013

Ehlers-Danlos syndromes and epilepsy: An updated review

artículo científico publicado en 2018

Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease

artículo científico publicado en 2019

Epileptic seizures in autosomal dominant forms of Alzheimer's disease

scientific article published on 19 July 2018

Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

artículo científico publicado en 2013

Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis

artículo científico publicado en 2011

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

From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

artículo científico publicado en 2011

GRN variability contributes to sporadic frontotemporal lobar degeneration

artículo científico publicado en 2010

GSK3β genetic variability in patients with Multiple Sclerosis

artículo científico publicado en 2011

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

Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2008

Investigating Cardiac Morphological Alterations in a Pentylenetetrazol-Kindling Model of Epilepsy

scientific article published on 09 June 2020

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

artículo científico publicado en 2010

Lymphocyte-Activation Gene 3 (LAG3) Protein as a Possible Therapeutic Target for Parkinson's Disease: Molecular Mechanisms Connecting Neuroinflammation to α-Synuclein Spreading Pathology

artículo científico publicado en 2020

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

artículo científico publicado en 2009

Molecular and Imaging Biomarkers in Alzheimer's Disease: A Focus on Recent Insights

artículo científico publicado en 2020

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration

artículo científico publicado en 2007

Novel exon 1 progranulin gene variant in Alzheimer's disease.

artículo científico

Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia

artículo científico publicado en 2013

Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia

artículo científico publicado en 2012

Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder

artículo científico publicado en 2014

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

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration

artículo científico publicado en 2009

The Progranulin (GRN) Cys157LysfsX97 Mutation is Associated with Nonfluent Variant of Primary Progressive Aphasia Clinical Phenotype

The Synergistic Relationship between Alzheimer's Disease and Sleep Disorders: An Update

artículo científico

Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing

scientific article published on 02 March 2019

and Nocturnal Frontal Lobe Epilepsy: Identification and Characterization of a Novel Loss of Function Mutation

artículo científico publicado en 2019

Lista de obras de Chiara Villa

A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia

Analysis of Human Papillomavirus (HPV) 16 Variants Associated with Cervical Infection in Italian Women

Arylsulfatase A (ASA) in Parkinson's Disease: From Pathogenesis to Biomarker Potential

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

Biomarkers for Alzheimer's Disease: Where Do We Stand and Where Are We Going?

C9ORF72 hexanucleotide repeat expansion as a rare cause of bipolar disorder

C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

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

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis

Candidate gene analysis of selectin cluster in patients with multiple sclerosis

Candidate gene analysis of semaphorins in patients with Alzheimer's disease

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

Circulating miRNAs as potential biomarkers in Alzheimer's disease

DCUN1D1 is a risk factor for frontotemporal lobar degeneration.

Decreased circulating miRNA levels in patients with primary progressive multiple sclerosis

Ehlers-Danlos syndromes and epilepsy: An updated review

Emerging roles of long non-coding RNAs in the pathogenesis of Alzheimer's disease

Epileptic seizures in autosomal dominant forms of Alzheimer's disease

Expression and Genetic Analysis of MicroRNAs Involved in Multiple Sclerosis

Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis

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

From genotype to phenotype: two cases of genetic frontotemporal lobar degeneration with premorbid bipolar disorder.

GRN variability contributes to sporadic frontotemporal lobar degeneration

GSK3β genetic variability in patients with Multiple Sclerosis

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

Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration

Investigating Cardiac Morphological Alterations in a Pentylenetetrazol-Kindling Model of Epilepsy

Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?

Lymphocyte-Activation Gene 3 (LAG3) Protein as a Possible Therapeutic Target for Parkinson's Disease: Molecular Mechanisms Connecting Neuroinflammation to α-Synuclein Spreading Pathology

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

Molecular and Imaging Biomarkers in Alzheimer's Disease: A Focus on Recent Insights

Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration

Novel exon 1 progranulin gene variant in Alzheimer's disease.

Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia

Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia

Progranulin gene variability influences the risk for bipolar I disorder, but not bipolar II disorder

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

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration

The Progranulin (GRN) Cys157LysfsX97 Mutation is Associated with Nonfluent Variant of Primary Progressive Aphasia Clinical Phenotype

The Synergistic Relationship between Alzheimer's Disease and Sleep Disorders: An Update

Understanding the basis of Ehlers-Danlos syndrome in the era of the next-generation sequencing

and Nocturnal Frontal Lobe Epilepsy: Identification and Characterization of a Novel Loss of Function Mutation