Lista de obras -

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

CSF β-amyloid as a putative biomarker of disease progression in multiple sclerosis

artículo científico publicado en 2016

CSF β-amyloid predicts prognosis in patients with multiple sclerosis

artículo científico publicado en 2018

Circulating miRNAs as potential biomarkers in Alzheimer's disease

artículo científico publicado en 2014

Effect of fingolimod treatment on circulating miR-15b, miR23a and miR-223 levels in patients with multiple sclerosis

artículo científico publicado en 2016

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

Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects

artículo científico publicado en 2014

Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes

artículo científico publicado en 2016

Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutations

artículo científico publicado en 2015

Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

artículo científico publicado en 2017

Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.

artículo científico publicado en 2016

The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementia

artículo científico publicado en 2015

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

artículo científico publicado en 2015

Lista de obras de

C9ORF72 hexanucleotide repeat expansion is a rare cause of schizophrenia

C9ORF72 repeat expansion not detected in patients with multiple sclerosis

CSF β-amyloid as a putative biomarker of disease progression in multiple sclerosis

CSF β-amyloid predicts prognosis in patients with multiple sclerosis

Circulating miRNAs as potential biomarkers in Alzheimer's disease

Effect of fingolimod treatment on circulating miR-15b, miR23a and miR-223 levels 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.

Incomplete penetrance of the C9ORF72 hexanucleotide repeat expansions: frequency in a cohort of geriatric non-demented subjects

Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.

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

Plasma Screening for Progranulin Mutations in Patients with Progressive Supranuclear Palsy and Corticobasal Syndromes

Profiling of ubiquitination pathway genes in peripheral cells from patients with frontotemporal dementia due to C9ORF72 and GRN mutations

Progranulin plasma levels predict the presence of GRN mutations in asymptomatic subjects and do not correlate with brain atrophy: results from the GENFI study

Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.

The novel GRN g.1159_1160delTG mutation is associated with behavioral variant frontotemporal dementia

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