Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Juri Balestrini"'
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Akademický článek
Dual Effect of PER2 C111G Polymorphism on Cognitive Functions across Progression from Subjective Cognitive Decline to Mild Cognitive Impairment
Autor: Salvatore Mazzeo, Valentina Bessi, Silvia Bagnoli, Giulia Giacomucci, Juri Balestrini, Sonia Padiglioni, Giulia Tomaiuolo, Assunta Ingannato, Camilla Ferrari, Laura Bracco, Sandro Sorbi, Benedetta Nacmias
Publikováno v: Diagnostics, Vol 11, Iss 4, p 718 (2021)
Background: Periodic circadian protein homolog 2 (PER2) has a role in the intracellular signaling pathways of long-term potentiation and has implications for synaptic plasticity. We aimed to assess the association of PER2 C111G polymorphism with cogn
Externí odkaz: https://doaj.org/article/dc1635a0dc3940f1bbd9eb4f5b857d84
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4
Alzheimer's Disease CSF Biomarker Profiles in Idiopathic Normal Pressure Hydrocephalus
Autor: Salvatore Mazzeo, Filippo Emiliani, Silvia Bagnoli, Sonia Padiglioni, Lorenzo Maria Del Re, Giulia Giacomucci, Juri Balestrini, Assunta Ingannato, Valentina Moschini, Carmen Morinelli, Giulia Galdo, Cristina Polito, Camilla Ferrari, Gastone Pansini, Alessandro Della Puppa, Sandro Sorbi, Benedetta Nacmias, Valentina Bessi
Publikováno v: Journal of Personalized Medicine; Volume 12; Issue 6; Pages: 935
Patients with idiopathic normal pressure hydrocephalus (iNPH) frequently show pathologic CSF Aβ42 levels, comparable with Alzheimer’s Disease (AD). Nevertheless, the clinical meaning of these findings has not been fully explained. We aimed to asse
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b95d926491752fac49d7fa659c815a73
https://pubmed.ncbi.nlm.nih.gov/35743720
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5
Huntingtin gene intermediate alleles influence the progression from subjective cognitive decline to mild cognitive impairment: A 14-year follow-up study
Autor: Salvatore Mazzeo, Filippo Emiliani, Silvia Bagnoli, Sonia Padiglioni, Vittoria Conti, Assunta Ingannato, Giulia Giacomucci, Juri Balestrini, Camilla Ferrari, Sandro Sorbi, Benedetta Nacmias, Valentina Bessi
Publikováno v: European journal of neurologyREFERENCES. 29(6)
Huntingtin (HTT) is a gene containing a key region of CAG repeats. HTT alleles containing from 27 to 35 CAG repeats are termed intermediate alleles (IAs). We aimed to assess the effect of IAs on progression of cognitive impairment in patients with su
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9129c22cd8c3011da70f8101881a8746
https://pubmed.ncbi.nlm.nih.gov/35181957
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6
Matching Clinical Diagnosis and Amyloid Biomarkers in Alzheimer’s Disease and Frontotemporal Dementia
Autor: Gemma Lombardi, Juri Balestrini, Benedetta Nacmias, Sonia Padiglioni, Valentina Bessi, Salvatore Mazzeo, Valentina Berti, Assunta Ingannato, Silvia Bagnoli, Camilla Ferrari, Giulia Giacomucci, Sandro Sorbi, Cristina Polito, Matteo Casini
Publikováno v: Journal of Personalized Medicine
Volume 11
Issue 1
Journal of Personalized Medicine, Vol 11, Iss 47, p 47 (2021)
Background: The aims of this study were to compare the diagnostic accuracy, sensitivity, specificity, and positive and negative predictive values (PPV, NPV) of different cerebrospinal fluid (CSF) amyloid biomarkers and amyloid-Positron Emission Tomog
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b12676516da2de054ff14f866760a91
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7
PER2 C111G polymorphism, cognitive reserve and cognition in subjective cognitive decline and mild cognitive impairment: a 10-year follow-up study
Autor: Benedetta Nacmias, Salvatore Mazzeo, Siro Bagnoli, Sonia Padiglioni, Giulia Giacomucci, Irene Piaceri, G. Tomaiuolo, Juri Balestrini, Valentina Bessi, Laura Bracco, Marco Carraro, Sandro Sorbi
Publikováno v: European journal of neurologyReferences. 28(1)
Background and purpose CLOCK and PER2 genes have been implicated in sleep-wake cycle alterations and neurodegenerative diseases. Our aim was to evaluate the effect of CLOCK T3111C and PER2 C111G on cognitive functioning in subjective cognitive declin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b4d1c5a140f3f4dc1c130772866ce4a
https://pubmed.ncbi.nlm.nih.gov/32896064
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8
Influence of
Autor: Valentina, Bessi, Juri, Balestrini, Silvia, Bagnoli, Salvatore, Mazzeo, Giulia, Giacomucci, Sonia, Padiglioni, Irene, Piaceri, Marco, Carraro, Camilla, Ferrari, Laura, Bracco, Sandro, Sorbi, Benedetta, Nacmias
Publikováno v: Journal of Personalized Medicine
Background: Some genes could interact with cardiovascular risk factors in the development of Alzheimer’s disease. We aimed to evaluate the interaction between ApoE ε4 status, Clock T3111C and Per2 C111G polymorphisms with cardiovascular profile in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dc49889b1296021842ca5d557ec88ef4
https://pubmed.ncbi.nlm.nih.gov/32485802
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9
Influence of ApoE Genotype and Clock T3111C Interaction with Cardiovascular Risk Factors on the Progression to Alzheimer’s Disease in Subjective Cognitive Decline and Mild Cognitive Impairment Patients
Autor: Laura Bracco, Juri Balestrini, Sonia Padiglioni, Irene Piaceri, Marco Carraro, Sandro Sorbi, Camilla Ferrari, Valentina Bessi, Benedetta Nacmias, Giulia Giacomucci, Silvia Bagnoli, Salvatore Mazzeo
Publikováno v: Journal of Personalized Medicine, Vol 10, Iss 45, p 45 (2020)
Journal of Personalized Medicine
Volume 10
Issue 2
Background: Some genes could interact with cardiovascular risk factors in the development of Alzheimer&rsquo
s disease. We aimed to evaluate the interaction between ApoE &epsilon
4 status, Clock T3111C and Per2 C111G polymorphisms with card
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42aaf00d27ebdc0441b1e530f86534eb
https://www.mdpi.com/2075-4426/10/2/45
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10
Dual Effect of PER2 C111G Polymorphism on Cognitive Functions across Progression from Subjective Cognitive Decline to Mild Cognitive Impairment
Autor: Giulia Tomaiuolo, Laura Bracco, Valentina Bessi, Sonia Padiglioni, Camilla Ferrari, Juri Balestrini, Sandro Sorbi, Silvia Bagnoli, Giulia Giacomucci, Assunta Ingannato, Salvatore Mazzeo, Benedetta Nacmias
Publikováno v: Diagnostics
Volume 11
Issue 4
Diagnostics, Vol 11, Iss 718, p 718 (2021)
Background: Periodic circadian protein homolog 2 (PER2) has a role in the intracellular signaling pathways of long-term potentiation and has implications for synaptic plasticity. We aimed to assess the association of PER2 C111G polymorphism with cogn
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::812b5462c83f08631a38f3e4ac670b1e
https://doi.org/10.3390/diagnostics11040718
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