GUERINI, FRANCA ROSA
GUERINI, FRANCA ROSA
HLA Allele Frequencies and Association with Severity of COVID-19 Infection in Northern Italian Patients
2022 F.R. Guerini, E. Bolognesi, A. Lax, L.N.C. Bianchi, A. Caronni, M. Zanzottera, C. Agliardi, M.P. Albergoni, P.I. Banfi, J. Navarro, M. Clerici
Blood Brain-Derived Neurotrophic Factor (BDNF) and Major Depression: Do We Have a Translational Perspective?
2021 B. Arosio, F.R. Guerini, R.C.O. Voshaar, I. Aprahamian
NK Cell Subpopulations and Receptor Expression in Recovering SARS-CoV-2 Infection
2021 M. Saresella, D. Trabattoni, I. Marventano, F. Piancone, F. La Rosa, A. Caronni, A. Lax, L. Bianchi, P. Banfi, J. Navarro, E. Bolognesi, M. Zanzottera, F.R. Guerini, M. Clerici
Can Serum Nitrosoproteome Predict Longevity of Aged Women?
2020 D. Capitanio, P. Barbacini, B. Arosio, F.R. Guerini, E. Torretta, F. Trecate, M. Cesari, D. Mari, M. Clerici, C. Gelfi
Vitamin D receptor polymorphisms in sex-frailty paradox
2020 B. Arosio, F.R. Guerini, A.S. Costa, A. Dicitore, E. Ferri, D. Mari, E. Torresani, M. Clerici, M. Cesari, G. Vitale
Editorial: Biomarkers to Disentangle the Physiological From Pathological Brain Aging
2020 F.R. Guerini, W.S. Lim, B. Arosio
Vitamin D Receptor Polymorphisms Associate with Autism Spectrum Disorder
2020 F. Guerini, E. Bolognesi, M. Chiappedi, M. Mensi, O. Fumagalli, M. Zanzottera, A. Ghezzo, M. Zanette, C. Agliardi, A. Costa, S. Sotgiu, A. Carta, N. Al Daghri, M. Clerici
Correction: BDNF rs6265 polymorphism methylation in Multiple Sclerosis: A possible marker of disease progression(PLoS ONE (2018) 1310 (e0206140) DOI: 10.1371/journal.pone.0206140)
2019 V. Nociti, M. Santoro, D. Quaranta, F.A. Losavio, C. De Fino, R. Giordano, N.P. Palomba, P.M. Rossini, F.R. Guerini, M. Clerici, D. Caputo, M. Mirabella
SNAP-25 in Serum Is Carried by Exosomes of Neuronal Origin and Is a Potential Biomarker of Alzheimer's Disease
2019 C. Agliardi, F.R. Guerini, M. Zanzottera, A. Bianchi, R. Nemni, M. Clerici
The Syntaxin-1A gene single nucleotide polymorphism rs4717806 associates with the risk of ischemic heart disease
2019 F.R. Guerini, E. Ripamonti, A.S. Costa, M. Zanzottera, C. Agliardi, E. Bolognesi, M. Clerici, V. Racca, O.C. Baltatu
HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication study
2019 F.R. Guerini, E. Bolognesi, S. Sotgiu, A. Carta, C. Clerici, M. Chiappedi, A. Ghezzo, M. Zanette, M.M. Mensi, M.P. Canevini, M. Zanzottera, C. Agliardi, A.S. Costa, U. Balottin, M. Clerici
SNARE Complex Polymorphisms Associate with Alterations of Visual Selective Attention in Alzheimer’s Disease
2019 A.S. Costa, F.R. Guerini, B. Arosio, D. Galimberti, M. Zanzottera, A. Bianchi, R. Nemni, M. Clerici
Association between Hippocampal Shape, Neuroinflammation, and Cognitive Decline in Alzheimer's Disease
2018 M. Cabinio, M. Saresella, F. Piancone, F. Larosa, I. Marventano, F.R. Guerini, R. Nemni, F. Baglio, M. Clerici
SNAP25 Gene Polymorphisms Protect Against Parkinson’s Disease and Modulate Disease Severity in Patients
2018 C. Agliardi, F.R. Guerini, M. Zanzottera, G. Riboldazzi, R. Zangaglia, A. Sturchio, C. Casali, C. Di Lorenzo, B. Minafra, R. Nemni, M. Clerici
HLA alleles modulate EBV viral load in multiple sclerosis
2018 S. Agostini, R. Mancuso, F.R. Guerini, S. D'Alfonso, C. Agliardi, A. Hernis, M. Zanzottera, N. Barizzone, M.A. Leone, D. Caputo, M. Rovaris, M. Clerici
TNF-α -308 G/A and -238 G/A promoter polymorphisms and sporadic Parkinson's disease in an Italian cohort
2018 C. Agliardi, F.R. Guerini, M. Zanzottera, G. Riboldazzi, R. Zangaglia, G. Bono, C. Casali, C. Di Lorenzo, C. Pacchetti, R. Nemni, M. Clerici
BDNF rs6265 polymorphism methylation in Multiple Sclerosis: A possible marker of disease progression
2018 V. Nociti, M. Santoro, D. Quaranta, F.A. Losavio, C. De Fino, R. Giordano, N. Palomba, P.M. Rossini, F.R. Guerini, M. Clerici, D. Caputo, M. Mirabella
Vitamin D-binding protein gene polymorphisms are not associated with MS risk in an Italian cohort
2017 C. Agliardi, F.R. Guerini, M. Zanzottera, E. Bolognesi, A.S. Costa, M. Clerici
Intermediate and low abundant protein analysis of vitamin D deficient obese and non-obese subjects by MALDI-profiling
2017 N.M. Al Daghri, E. Torretta, D. Capitanio, C. Fania, F.R. Guerini, S.B. Sabico, M.S. Clerici, C. Gelfi
A common genetic variant in FOXP2 is associated with language-based learning (dis)abilities : Evidence from two Italian independent samples
2017 A. Mozzi, V. Riva, D. Forni, M. Sironi, C. Marino, M. Molteni, S. Riva, F.R. Guerini, M. Clerici, R. Cagliani, S. Mascheretti