Franca Vasso

发表

Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutation.

A. Bruni, M. Anfossi, L. Bernardi, 2013, Journal of Alzheimer's Disease.

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

F. Tagliavini, A. Bruni, O. Bugiani, 2011, Journal of Alzheimer's disease : JAD.

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

C. Cupidi, A. Bruni, M. Anfossi, 2014, Neurobiology of Aging.

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

S. Sorbi, B. Nacmias, C. Cupidi, 2017, Neurobiology of Aging.

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

C. Cupidi, A. Bruni, M. Anfossi, 2016, Journal of Alzheimer's disease : JAD.

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

A. Bruni, M. Anfossi, L. Bernardi, 2010, Neurological Sciences.

Phenotypic expressions of Alzheimer’s disease: a gender perspective

C. Cupidi, A. Bruni, M. Anfossi, 2018 .

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

C. Cupidi, A. Bruni, M. Anfossi, 2015, Neurology.

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

C. Cupidi, A. Bruni, M. Anfossi, 2018, Journal of Alzheimer's disease : JAD.

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

A. Bruni, M. Anfossi, L. Bernardi, 2009, Journal of Alzheimer's disease : JAD.