A. Clodomiro

发表

Genetic variation in the myeloperoxidase gene and cognitive impairment in Multiple Sclerosis

A. Quattrone, F. Condino, M. Liguori, 2006, Journal of Negative Results in BioMedicine.

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.

PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype.

A. Bruni, M. Anfossi, L. Bernardi, 2011, Journal of Alzheimer's disease : JAD.

Impact of individual cognitive profile on visuo-motor reorganization in relapsing–remitting multiple sclerosis

L. Passamonti, F. Fera, A. Cerasa, 2007, Brain Research.

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.

An adenovirus carrying the rat protein tyrosine phosphatase eta suppresses the growth of human thyroid carcinoma cell lines in vitro and in vivo.

G. Viglietto, M. Santoro, A. Fusco, 2003, Cancer research.

Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P)

A. Quattrone, M. Muglia, M. Zappia, 2005, Neurology.

Investigating the role of brain‐derived neurotrophic factor in relapsing–remitting multiple sclerosis

F. Fera, A. Cerasa, M. C. Gioia, 2007, Genes, brain, and behavior.

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

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

Adaptive cortical changes and the functional correlates of visuo-motor integration in relapsing-remitting multiple sclerosis

Francesco Fera, Antonio Cerasa, Aldo Quattrone, 2006, Brain Research Bulletin.

Worldwide distribution of PSEN1 Met146Leu mutation

S. Pappatà, S. Sorbi, G. Forloni, 2010, Neurology.

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

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

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

G. Comi, S. Cappa, M. Filippi, 2013, Biological Psychiatry.

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

E. Rogaeva, P. George-Hyslop, C. Cupidi, 2012, Neurobiology of Aging.

Somatic comorbidities and Alzheimer’s disease treatment

A. Bruni, F. Frangipane, P. Gareri, 2013, Neurological Sciences.

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.

P. Mecocci, A. Bruni, N. Smirne, 2017, Journal of Alzheimer's disease : JAD.

Preliminary evidences of a NOS2A protective effect from Relapsing–Remitting Multiple Sclerosis

A. Quattrone, F. Condino, M. Liguori, 2008, Journal of the Neurological Sciences.

The role of VLA4 polymorphisms in multiple sclerosis: An association study

A. Quattrone, P. Spadafora, F. Condino, 2007, Journal of Neuroimmunology.

Autosomal Dominant Frontotemporal Lobar Degeneration Due to the C9ORF72 Hexanucleotide Repeat Expansion: Late-Onset Psychotic Clinical Presentation

M. Filippi, M. Franceschi, F. Agosta, 2013, Biological Psychiatry.

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

P. Mecocci, A. Bruni, N. Smirne, 2017, Alzheimer's & Dementia.