List of works - Chiara Cupidi

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

scientific article

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

scientific article published on January 2014

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

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

scientific article

Brain-derived neurotrophic factor modulates cholesterol homeostasis and Apolipoprotein E synthesis in human cell models of astrocytes and neurons

scientific article published on 11 January 2018

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

scientific article published on 23 January 2017

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

scientific article published on 20 July 2012

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

scientific article published in January 2018

Frontal dementia related to thalamic stroke: a case report.

scientific article published on 5 July 2012

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

scientific article

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 28 February 2019

Haptoglobin interacts with apolipoprotein E and beta-amyloid and influences their crosstalk

scientific article published in August 2014

Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

scientific article published on August 2010

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

scientific article published on 6 May 2015

Lipofuscin hypothesis of Alzheimer's disease.

scientific article

NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's disease.

scientific article published on 13 April 2016

Neocortical variation of Abeta load in fully expressed, pure Alzheimer's disease.

scientific article published in January 2010

Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.

scientific article published in March 2004

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

scientific article published on 14 June 2014

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

scientific article published on 20 November 2017

REM sleep behavior disorder in a patient with frontotemporal dementia ⬇️

scientific article published on July 13, 2011

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

scientific article

Role of Niemann-Pick Type C Disease Mutations in Dementia

scientific article published on 24 October 2016

Sleep quality in caregivers of patients with Alzheimer's disease and Parkinson's disease and its relationship to quality of life

scientific article published in June 2012

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

scientific article published on 27 April 2017

List of works by Chiara Cupidi

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.

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

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

Brain-derived neurotrophic factor modulates cholesterol homeostasis and Apolipoprotein E synthesis in human cell models of astrocytes and neurons

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.

Frontal dementia related to thalamic stroke: a case report.

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

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Haptoglobin interacts with apolipoprotein E and beta-amyloid and influences their crosstalk

Hereditary cerebral hemorrhage with amyloidosis associated with the E693K mutation of APP.

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

Lipofuscin hypothesis of Alzheimer's disease.

NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's disease.

Neocortical variation of Abeta load in fully expressed, pure Alzheimer's disease.

Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 gene.

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

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

REM sleep behavior disorder in a patient with frontotemporal dementia ⬇️

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Role of Niemann-Pick Type C Disease Mutations in Dementia

Sleep quality in caregivers of patients with Alzheimer's disease and Parkinson's disease and its relationship to quality of life

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