Search Results - "GUERINI, F"

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    Clinical Presentation of COVID19 in Dementia Patients by Bianchetti, Angelo, Rozzini, R., Guerini, F., Boffelli, S., Ranieri, P., Minelli, G., Bianchetti, L., Trabucchi, M.

    Published in The Journal of nutrition, health & aging (01-06-2020)
    “…Objective No studies analyzing the role of dementia as a risk factor for mortality in patients affected by COVID-19. We assessed the prevalence, clinical…”
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    Journal Article
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    Association between SNAP-25 gene polymorphisms and cognition in autism: functional consequences and potential therapeutic strategies by Braida, D, Guerini, F R, Ponzoni, L, Corradini, I, De Astis, S, Pattini, L, Bolognesi, E, Benfante, R, Fornasari, D, Chiappedi, M, Ghezzo, A, Clerici, M, Matteoli, M, Sala, M

    Published in Translational psychiatry (27-01-2015)
    “…Synaptosomal-associated protein of 25 kDa (SNAP-25) is involved in different neuropsychiatric disorders, including schizophrenia and…”
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    Journal Article
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    A prognostic model predicting recovery of walking independence of elderly patients after hip-fracture surgery. An experiment in a rehabilitation unit in Northern Italy by Bellelli, G., Noale, M., Guerini, F., Turco, R., Maggi, S., Crepaldi, G., Trabucchi, M.

    Published in Osteoporosis international (01-08-2012)
    “…Summary A score for identifying post-hip-fracture surgery patients at various levels (high, medium, and low) of risk for unsuccessful recovery of pre-fracture…”
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    Journal Article
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    BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease by Guerini, F. R., Beghi, E., Riboldazzi, G., Zangaglia, R., Pianezzola, C., Bono, G., Casali, C., Di Lorenzo, C., Agliardi, C., Nappi, G., Clerici, M., Martignoni, E.

    Published in European journal of neurology (01-11-2009)
    “…Background and purpose:  A possible association between Parkinson’s disease (PD) and the polymorphism of Brain Derived Neurotrophic Factor (BDNF) G196A…”
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    Journal Article
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    Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency by GIRONI, M, LAMPERTI, C, DIMAURO, S, NEMNI, R, MOGGIO, M, COMI, G, GUERINI, F. R, FERRANTE, P, CANAL, N, NAINI, A, BRESOLIN, N

    Published in Neurology (09-03-2004)
    “…Two brothers had late-onset progressive ataxia, cerebellar atrophy, and hypergonadotropic hypogonadism associated with coenzyme Q10 (CoQ10) deficiency in…”
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    Journal Article
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    HLA-class I markers and multiple sclerosis susceptibility in the Italian population by Bergamaschi, L, Leone, M A, Fasano, M E, Guerini, F R, Ferrante, D, Bolognesi, E, Barizzone, N, Corrado, L, Naldi, P, Agliardi, C, Dametto, E, Salvetti, M, Visconti, A, Galimberti, D, Scarpini, E, Vercellino, M, Bergamaschi, R, Monaco, F, Caputo, D, Momigliano-Richiardi, P, D'Alfonso, S

    Published in Genes and immunity (01-03-2010)
    “…Previous studies reported an association with multiple sclerosis (MS) of distinct HLA-class I markers, namely HLA-A*02 , HLA-Cw*05 and MOG-142L . In this work,…”
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    Journal Article
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    Variations of the perforin gene in patients with multiple sclerosis by Cappellano, G, Orilieri, E, Comi, C, Chiocchetti, A, Bocca, S, Boggio, E, Bernardone, I S, Cometa, A, Clementi, R, Barizzone, N, D'Alfonso, S, Corrado, L, Galimberti, D, Scarpini, E, Guerini, F R, Caputo, D, Paolicelli, D, Trojano, M, Figà-Talamanca, L, Salvetti, M, Perla, F, Leone, M, Monaco, F, Dianzani, U

    Published in Genes and immunity (01-07-2008)
    “…Perforin is involved in cell-mediated cytotoxicity and mutations of its gene ( PRF1 ) cause familial hemophagocytic lymphohistiocytosis (FLH2). PRF1 sequencing…”
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    Journal Article
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    HLA-A01 is associated with late onset of Alzheimer's disease in Italian patients by Guerini, F R, Tinelli, C, Calabrese, E, Agliardi, C, Zanzottera, M, De Silvestri, A, Franceschi, M, Grimaldi, L M E, Nemni, R, Clerici, M

    “…In this study, the distribution of HLA-A alleles was analyzed in Italian Alzheimer's Disease (AD)patients. Interaction between HLA alleles, APOE genotypes, age…”
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    Mutations in the lamin B1 gene are not present in multiple sclerosis by Brussino, A., D'Alfonso, S., Cagnoli, C., Di Gregorio, E., Barberis, M., Padovan, S., Vaula, G., Pinessi, L., Squadrone, S., Abete, M. C., Collimedaglia, L., Guerini, F. R., Migone, N., Brusco, A.

    Published in European journal of neurology (01-04-2009)
    “…Background:  Whole gene duplication of the lamin B1 gene (LMNB1), encoding for a protein of the nuclear lamina, causes an adult‐onset autosomal dominant…”
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    Journal Article
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    HLA-DRB11501 and response to copolymer-1 therapy in relapsing-remitting multiple sclerosis by FUSCO, C, ANDREONE, V, VIVO, P, MINI, M, MACRI, M, OREFICE, G, LOMBARDI, M. L, COPPOLA, G, LUONGO, V, GUERINI, F, PACE, E, FLORIO, C, PIROZZI, G, LANZILLO, R, FERRANTE, P

    Published in Neurology (11-12-2001)
    “…Copolymer 1 (Cop-1) is a random synthetic amino acid copolymer, effective in the treatment of the relapsing-remitting form of MS (RRMS). In vitro and in vivo…”
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    Journal Article
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    A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy by D'Alfonso, S, Bolognesi, E, Guerini, F R, Barizzone, N, Bocca, S, Ferrante, D, Castelli, L, Bergamaschi, L, Agliardi, C, Ferrante, P, Naldi, P, Leone, M, Caputo, D, Ballerini, C, Salvetti, M, Galimberti, D, Massacesi, L, Trojano, M, Momigliano-Richiardi, P

    Published in Genes and immunity (01-01-2008)
    “…Several studies suggest that the histocompatibility complex (HLA) class I region harbours genes modulating multiple sclerosis (MS) susceptibility independently…”
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    Journal Article
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    HLA-DRB1 polymorphisms distribution in chronic dysimmune polyneuropathy by Gironi, M, Guerini, F.R, Beghi, E, Antonini, G, Martinelli-Boneschi, F, Ceresa, L, Morino, S, Agliardi, C, Ferrante, P, Nemni, R

    Published in Neuromuscular disorders : NMD (01-12-2008)
    “…Abstract The frequency of HLA-DRB1∗ 15 polymorphism, which is strongly associated to multiple sclerosis, was investigated in 84 adult patients with chronic…”
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    Journal Article
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    Myelin basic protein gene is associated with MS in DR4- and DR5-positive Italians and Russians by Guerini, F R, Ferrante, P, Losciale, L, Caputo, D, Lombardi, M L, Pirozzi, G, Luongo, V, Sudomoina, M A, Andreewski, T V, Alekseenkov, A D, Boiko, A N, Gusev, E I, Favorova, O O

    Published in Neurology (26-08-2003)
    “…The myelin basic protein (MBP) gene may confer genetic susceptibility to multiple sclerosis (MS). The association of MS with alleles of the (TGGA)n variable…”
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    Journal Article
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