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

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

artículo científico

Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia

scientific article published on 03 February 2011

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

artículo científico publicado en 2017

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

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.

artículo científico publicado en 2016

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

Investigation of c9orf72 in 4 neurodegenerative disorders

artículo científico publicado en 2012

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

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

Somatic comorbidities and Alzheimer's disease treatment.

scientific article published on February 2013

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients

artículo científico publicado en 2015

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

Uncoupling protein 4 () gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia

article

Usefulness of movement time in the assessment of Parkinson's disease

artículo científico publicado en 1994

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.

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

Compound heterozygosity of 2 novel MAPT mutations in frontotemporal dementia

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.

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.

Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.

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

Investigation of c9orf72 in 4 neurodegenerative disorders

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

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

Somatic comorbidities and Alzheimer's disease treatment.

The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients

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.

Uncoupling protein 4 () gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementia

Usefulness of movement time in the assessment of Parkinson's disease