about
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease familyAngela R.: a familial Alzheimer's disease case in the days of Auguste D.Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy.Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degeneration.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.AbetaPP A713T mutation in late onset Alzheimer's disease with cerebrovascular lesions.Prevalence of Delirium in a Population of Elderly Outpatients with Dementia: A Retrospective Study.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.Frequency of Cardiovascular Genetic Risk Factors in a Calabrian Population and Their Effects on Dementia.The novel PSEN1 M84V mutation associated to frontal dysexecutive syndrome, spastic paraparesis, and cerebellar atrophy in a dominant Alzheimer's disease family.A novel pathogenic PSEN1 mutation in a family with Alzheimer's disease: phenotypical and neuropathological features.Role of Niemann-Pick Type C Disease Mutations in Dementia.Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutationThe effects of APOE and tau gene variability on risk of frontotemporal dementiaNovel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementiaPresenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's diseasePSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotypeMAPT V363I variation in a sporadic case of frontotemporal dementia: variable penetrant mutation or rare polymorphism?Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndrome
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P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Nicoletta Smirne
@en
Nicoletta Smirne
@nl
type
label
Nicoletta Smirne
@en
Nicoletta Smirne
@nl
prefLabel
Nicoletta Smirne
@en
Nicoletta Smirne
@nl
P31
P496
0000-0003-4645-9960