Search Results - "GUERINI, F"
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1
Clinical Presentation of COVID19 in Dementia Patients
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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2
Letter to the Editor Regarding: Enhancing Telemedicine to Improve Global Radiotherapy Access
Published in Clinical oncology (Royal College of Radiologists (Great Britain)) (01-09-2024)Get full text
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3
Association between SNAP-25 gene polymorphisms and cognition in autism: functional consequences and potential therapeutic strategies
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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4
Burden of rare coding variants in an Italian cohort of familial multiple sclerosis
Published in Journal of neuroimmunology (15-01-2022)“…Multiple Sclerosis (MS) is a chronic inflammatory and neurodegenerative demyelinating disease of the central nervous system. It is a complex and heterogeneous…”
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5
A prognostic model predicting recovery of walking independence of elderly patients after hip-fracture surgery. An experiment in a rehabilitation unit in Northern Italy
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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BDNF Val66Met polymorphism is associated with cognitive impairment in Italian patients with Parkinson's disease
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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7
Analysis of genes, pathways and networks involved in disease severity and age at onset in primary-progressive multiple sclerosis
Published in Multiple sclerosis (01-10-2015)“…Background: The role of genetic factors in influencing the clinical expression of multiple sclerosis (MS) is unclear. Objective: The objective of this paper is…”
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8
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency
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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9
HLA-class I markers and multiple sclerosis susceptibility in the Italian population
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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10
A trans-specific polymorphism in ZC3HAV1 is maintained by long-standing balancing selection and may confer susceptibility to multiple sclerosis
Published in Molecular biology and evolution (01-06-2012)“…The human ZC3HAV1 gene encodes an antiviral protein. The longest splicing isoform of ZC3HAV1 contains a C-terminal PARP-like domain, which has evolved under…”
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11
A pathological evaluation of peritoneal carcinomatosis
Published in European journal of surgical oncology (01-10-2012)Get full text
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12
Variations of the perforin gene in patients with multiple sclerosis
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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13
HLA-A01 is associated with late onset of Alzheimer's disease in Italian patients
Published in International journal of immunopathology and pharmacology (01-10-2009)“…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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14
Mutations in the lamin B1 gene are not present in multiple sclerosis
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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15
HLA-DRB11501 and response to copolymer-1 therapy in relapsing-remitting multiple sclerosis
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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16
A sequence variation in the MOG gene is involved in multiple sclerosis susceptibility in Italy
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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17
HLA-DRB1 polymorphisms distribution in chronic dysimmune polyneuropathy
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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18
Myelin basic protein gene is associated with MS in DR4- and DR5-positive Italians and Russians
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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CEREBROVASCULAR DISEASE AND EXECUTIVE DYSFUNCTION IN GERIATRIC DEPRESSION
Published in The journals of gerontology. Series A, Biological sciences and medical sciences (01-12-2005)Get full text
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Validation of the 4AT, a new instrument for rapid delirium screening: a study in 234 hospitalised older people
Published in Age and ageing (01-07-2014)“…to evaluate the performance of the 4 'A's Test (4AT) in screening for delirium in older patients. The 4AT is a new test for rapid screening of delirium in…”
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