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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|September 22, 2009
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementiaMaura Gallo, Carmine Tomaino, Gianfranco Puccio, et al.
Plos One|May 16, 2015
Pectate lyase pollen allergens: sensitization profiles and cross-reactivity patternUlrike Pichler, Michael Hauser, Martin Wolf, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 23, 2019
The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italySilvia Grimaldi, Chiara Cupidi, Nicoletta Smirne, et al.
Journal of Alzheimer'S Disease : JAD|February 8, 2014
Association of the variant Cys139Arg at GRN gene to the clinical spectrum of frontotemporal lobar degenerationIrene Piaceri, Silvia Pradella, Chiara Cupidi, et al.
Plos One|November 25, 2011
Allergenic lipid transfer proteins from plant-derived foods do not immunologically and clinically behave homogeneously: the kiwifruit LTP as a modelMaria Livia Bernardi, Ivana Giangrieco, Laura Camardella, et al.
Journal of Alzheimer'S Disease : JAD|February 8, 2011
PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotypeLivia Bernardi, Maria Anfossi, Maura Gallo, et al.
Neurobiology of Aging|March 4, 2008
Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementiaLivia Bernardi, Carmine Tomaino, Maria Anfossi, et al.
Journal of Alzheimer'S Disease : JAD|June 25, 2013
Role of TOMM40 rs10524523 polymorphism in onset of alzheimer's disease caused by the PSEN1 M146L mutationLivia Bernardi, Maura Gallo, Maria Anfossi, et al.
Neurobiology of Aging|July 16, 2014
Novel N-terminal domain mutation in prion protein detected in 2 patients diagnosed with frontotemporal lobar degeneration syndromeLivia Bernardi, Chiara Cupidi, Francesca Frangipane, et al.
The Journal of Clinical Endocrinology and Metabolism|July 29, 2011
Clinical manifestations of highly prevalent corticosteroid-binding globulin mutations in a village in southern ItalyGiovanni Cizza, Livia Bernardi, Nicoletta Smirne, et al.
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