Lista de obras -

A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.

artículo científico publicado en 2011

AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.

artículo científico publicado en 2009

Angela R.: a familial Alzheimer's disease case in the days of Auguste D.

artículo científico publicado en 2016

Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.

artículo científico

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

scientific article published on 17 September 2020

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.

artículo científico publicado en 2012

Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.

artículo científico publicado en 2018

Frontotemporal dementia and its subtypes: a genome-wide association study

artículo científico publicado en 2014

Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation

article

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

artículo científico publicado en 2015

Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.

artículo científico publicado en 2008

MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?

artículo científico publicado en 2011

Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia

artículo científico publicado en 2009

Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome

artículo científico publicado en 2014

PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype

artículo científico publicado en 2011

Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease

artículo científico publicado en 2007

Prevalence of Delirium in a Population of Elderly Outpatients with Dementia: A Retrospective Study

artículo científico publicado en 2017

Role of Niemann-Pick Type C Disease Mutations in Dementia.

artículo científico publicado en 2016

Short-Term Response is not Predictive of Long-Term Response to Acetylcholinesterase Inhibitors in Old Age Subjects with Alzheimer's Disease: A "Real World" Study

artículo científico publicado en 2016

The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 Carriers.

artículo científico publicado en 2016

The effects of APOE and tau gene variability on risk of frontotemporal dementia

article

The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.

artículo científico publicado en 2017

Lista de obras de

A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.

AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.

Angela R.: a familial Alzheimer's disease case in the days of Auguste D.

Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.

C9orf72, AAO and ancestry help discriminating behavioural from language variants in FTLD cohorts

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.

Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.

Frontotemporal dementia and its subtypes: a genome-wide association study

Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.

MAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?

Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia

Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome

PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype

Presenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's disease

Prevalence of Delirium in a Population of Elderly Outpatients with Dementia: A Retrospective Study

Role of Niemann-Pick Type C Disease Mutations in Dementia.

Short-Term Response is not Predictive of Long-Term Response to Acetylcholinesterase Inhibitors in Old Age Subjects with Alzheimer's Disease: A "Real World" Study

The Genetic Variability of UCP4 Affects the Individual Susceptibility to Late-Onset Alzheimer's Disease and Modifies the Disease's Risk in APOE-ɛ4 Carriers.

The effects of APOE and tau gene variability on risk of frontotemporal dementia

The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.