about
Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease familySomatic comorbidities and Alzheimer's disease treatment.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.Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.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.Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol.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.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 dementiaUncoupling protein 4 () gene variability in neurodegenerative disorders: further evidence of association in Frontotemporal dementiaCompound heterozygosity of 2 novel MAPT mutations in frontotemporal dementiaNovel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementiaUsefulness of movement time in the assessment of Parkinson's diseasePresenilin 2 Ser130Leu mutation in a case of late-onset "sporadic" Alzheimer's diseaseMAPT 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
P50
Q35686163-D8CBD565-D91D-4A3F-AAFE-B799106194BDQ37199794-7D8044E1-CC6C-4D58-95CE-7C46AE09FAA9Q37248850-4F606414-6619-4CC6-BD93-6EFEEF8A929BQ38436704-97AABE47-F6B3-4736-AD99-13ADCB8437DEQ38765067-C874A493-9051-4921-8E67-590D42555C13Q39962778-22A5C0E5-D8DB-4E25-AFEC-0E32FB7BD8A4Q40895731-6DB745AA-3E25-4DF4-B25B-F473AD8F232FQ45223489-09A5C03D-8279-4916-A945-A9AAE5DF43FDQ47419328-03B41A8C-3B9E-4006-BD6E-5D33493EA6C8Q50053711-521A5F66-721D-413D-BB94-F44F191F6ECDQ50987809-A9F7D391-B348-4D9E-8237-3E9D852A57EFQ51808482-0CA38EA2-3D63-4A4E-853A-C8B325237401Q52964979-21DF2CAB-C3D3-4B58-8964-C16F49692712Q53392174-FD8E11DF-5B5A-49EC-8313-A565DD0E5175Q57419060-2BF539BC-980D-4E1E-A0A4-B74FBD5864F0Q57419079-0E946EB1-FFB3-409F-AD06-8A2A71C129D0Q60054668-B217CEF5-DDBA-4DCC-A55B-32761207F9B9Q61853781-35CFCC69-F304-45BE-9FB9-B6DAA61DB7A6Q61853785-E6C477E1-14A9-4895-9BA5-3D285FC81149Q62782482-D48DE072-AB98-4FAA-A96D-ACB787F68FE4Q79898162-1ED41FCA-2F87-4C4B-889E-E3E17CF6E34EQ83462275-848468B4-B7FE-4A87-BE0D-B819BCBE43F9Q87398752-58FDF8CE-B44E-4251-9676-F7F1D5350838
P50
description
researcher
@en
wetenschapper
@nl
name
R Colao
@en
R Colao
@nl
type
label
R Colao
@en
R Colao
@nl
prefLabel
R Colao
@en
R Colao
@nl
P106
P31
P496
0000-0002-3532-0659