Lista de obras - Federica Esposito - Dominio Público Uruguay

A genome-wide association study in progressive multiple sclerosis

scientific journal article

A pharmacogenetic study implicates SLC9a9 in multiple sclerosis disease activity

artículo científico publicado en 2015

An APOE haplotype associated with decreased ε4 expression increases the risk of late onset Alzheimer's disease

artículo científico publicado en 2011

Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis.

artículo científico publicado en 2015

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

artículo científico publicado en 2013

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans

artículo científico publicado en 2012

Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients

artículo científico publicado en 2013

Clinical and MRI predictors of response to interferon-beta and glatiramer acetate in relapsing-remitting multiple sclerosis patients.

artículo científico publicado en 2013

Clinical deterioration due to co-occurrence of multiple sclerosis and glioblastoma: report of two cases.

artículo científico publicado en 2016

Clinical response to Nabiximols correlates with the downregulation of immune pathways in multiple sclerosis.

artículo científico publicado en 2018

Comparative study of mitoxantrone efficacy profile in patients with relapsing—remitting and secondary progressive multiple sclerosis ⬇️

artículo científico publicado el 1 de septiembre de 2010

Efficacy and safety of nabiximols (Sativex(®)) on multiple sclerosis spasticity in a real-life Italian monocentric study.

artículo científico publicado en 2015

Familial clustering in Italian progressive-onset and bout-onset multiple sclerosis

artículo científico publicado en 2014

Functional and structural plasticity following action observation training in multiple sclerosis

scientific article published on 07 August 2018

GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.

artículo científico publicado en 2013

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

artículo científico publicado en 2011

Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis

artículo científico publicado en 2018

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

artículo científico publicado en 2011

Imaging correlates of hand motor performance in multiple sclerosis: A multiparametric structural and functional MRI study

artículo científico publicado en 2019

Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population

artículo científico publicado en 2010

Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis

scientific article published on 22 December 2014

Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort

artículo científico publicado en 2010

Low frequency and rare coding variation contributes to multiple sclerosis risk

MGAT5 alters the severity of multiple sclerosis

scientific journal article

MGAT5 and disease severity in progressive multiple sclerosis

artículo científico publicado en 2010

MRI correlates of clinical disability and hand-motor performance in multiple sclerosis phenotypes

artículo científico publicado en 2020

MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers

artículo científico publicado en 2011

Neuromyelitis optica spectrum disorders: long-term safety and efficacy of rituximab in Caucasian patients

artículo científico publicado en 2015

Pharmacogenetic study of long-term response to interferon-β treatment in multiple sclerosis.

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males

article

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

scholarly article published 13 July 2017

The burden of multiple sclerosis variants in continental Italians and Sardinians

artículo científico publicado en 2015

Uncovering the genetic architecture of multiple sclerosis.

artículo científico publicado en 2010

Lista de obras de Federica Esposito

A genome-wide association study in progressive multiple sclerosis

A pharmacogenetic study implicates SLC9a9 in multiple sclerosis disease activity

An APOE haplotype associated with decreased ε4 expression increases the risk of late onset Alzheimer's disease

Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis.

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

Association between DPP6 polymorphism and the risk of progressive multiple sclerosis in Northern and Southern Europeans

Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients

Clinical and MRI predictors of response to interferon-beta and glatiramer acetate in relapsing-remitting multiple sclerosis patients.

Clinical deterioration due to co-occurrence of multiple sclerosis and glioblastoma: report of two cases.

Clinical response to Nabiximols correlates with the downregulation of immune pathways in multiple sclerosis.

Comparative study of mitoxantrone efficacy profile in patients with relapsing—remitting and secondary progressive multiple sclerosis ⬇️

Efficacy and safety of nabiximols (Sativex(®)) on multiple sclerosis spasticity in a real-life Italian monocentric study.

Familial clustering in Italian progressive-onset and bout-onset multiple sclerosis

Functional and structural plasticity following action observation training in multiple sclerosis

GNAL deletion as a probable cause of dystonia in a patient with the 18p- syndrome.

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Genome sequencing uncovers phenocopies in primary progressive multiple sclerosis

Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci

Imaging correlates of hand motor performance in multiple sclerosis: A multiparametric structural and functional MRI study

Immunoproteasome LMP2 60HH variant alters MBP epitope generation and reduces the risk to develop multiple sclerosis in Italian female population

Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis

Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort

Low frequency and rare coding variation contributes to multiple sclerosis risk

MGAT5 alters the severity of multiple sclerosis

MGAT5 and disease severity in progressive multiple sclerosis

MRI correlates of clinical disability and hand-motor performance in multiple sclerosis phenotypes

MicroRNA and mRNA expression profile screening in multiple sclerosis patients to unravel novel pathogenic steps and identify potential biomarkers

Neuromyelitis optica spectrum disorders: long-term safety and efficacy of rituximab in Caucasian patients

Pharmacogenetic study of long-term response to interferon-β treatment in multiple sclerosis.

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

Progranulin gene variability increases the risk for primary progressive multiple sclerosis in males

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

The burden of multiple sclerosis variants in continental Italians and Sardinians

Uncovering the genetic architecture of multiple sclerosis.