Zobrazeno 1 - 10
of 200
pro vyhledávání: '"Nilo Riva"'
Autor:
Davide De Federicis, Claudia Bassani, Rosaria Rita Chiarelli, Federico Montini, Antonino Giordano, Federica Esposito, Nilo Riva, Angelo Quattrini, Vittorio Martinelli, Massimo Filippi, Cinthia Farina
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Neurological disorders, including multiple sclerosis (MS) and amyotrophic lateral sclerosis (ALS), may be associated with alterations in blood cell composition and phenotype. Here, we focused our attention on circulating mucosal-associated invariant
Externí odkaz:
https://doaj.org/article/5284a7c32dda470db8b419159ba98497
Autor:
Veronica Castelnovo, Elisa Canu, Teuta Domi, Laura Pozzi, Francesca Vignaroli, Edoardo Gioele Spinelli, Alma Ghirelli, Giacomo Tondo, Cristoforo Comi, Nilo Riva, Angelo Quattrini, Paola Carrera, Massimo Filippi, Federica Agosta
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
ObjectivesWe report the clinical presentation and evolution of a case with a novel Progranulin gene (GRN) mutation and non-fluent language disturbances at onset.Materials and methodsA 60 year-old, white patient was followed due to a history of langua
Externí odkaz:
https://doaj.org/article/77c9dbf4a92346699008b24676a4b734
Autor:
Giovanni Napoli, Martina Rubin, Gianni Cutillo, Paride Schito, Tommaso Russo, Angelo Quattrini, Massimo Filippi, Nilo Riva
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 15, p 12096 (2023)
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease with variable phenotypic expressions which has been associated with autonomic dysfunction. The cardiovascular system seems to be affected especially in the context of bulbar involveme
Externí odkaz:
https://doaj.org/article/c900c1a228fa4eef9bf197213491d7f1
Autor:
Federica Cerri, Francesco Gentile, Ferdinando Clarelli, Silvia Santoro, Yuri Matteo Falzone, Giorgia Dina, Alessandro Romano, Teuta Domi, Laura Pozzi, Raffaella Fazio, Paola Podini, Melissa Sorosina, Paola Carrera, Federica Esposito, Nilo Riva, Chiara Briani, Tiziana Cavallaro, Massimo Filippi, Angelo Quattrini
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
Although inflammation appears to play a role in neurolymphomatosis (NL), the mechanisms leading to degeneration in the peripheral nervous system are poorly understood. The purpose of this exploratory study was to identify molecular pathways underlyin
Externí odkaz:
https://doaj.org/article/cc6f17e7176d4a779b5afbb6b7aa98d8
Autor:
Edoardo Gioele Spinelli, Alma Ghirelli, Nilo Riva, Elisa Canu, Veronica Castelnovo, Teuta Domi, Laura Pozzi, Paola Carrera, Vincenzo Silani, Adriano Chiò, Massimo Filippi, Federica Agosta
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
ObjectiveMutations in the TARDBP gene are a rare cause of genetic motor neuron disease (MND). Morphologic MRI characteristics of MND patients carrying this mutation have been poorly described. Our objective was to investigate distinctive clinical and
Externí odkaz:
https://doaj.org/article/6047c59f82b24d8bb3680aaeef13b7bb
Autor:
Benedetta Storti, Susanna Diamanti, Lucio Tremolizzo, Nilo Riva, Christian Lunetta, Massimo Filippi, Carlo Ferrarese, Ildebrando Appollonio
Publikováno v:
Case Reports in Neurology, Vol 13, Iss 1, Pp 145-156 (2021)
Amyotrophic lateral sclerosis (ALS) is a clinically heterogeneous disease, with chameleon presentations and several mimics. Considering the poor prognosis of ALS, their precise and timely identification is pivotal. Affection of the cervical spine rep
Externí odkaz:
https://doaj.org/article/936c56a3fe2144259846183fe59fb79b
Autor:
Nilo Riva, Laura Pozzi, Tommaso Russo, Giovanni Battista Pipitone, Paride Schito, Teuta Domi, Federica Agosta, Angelo Quattrini, Paola Carrera, Massimo Filippi
Publikováno v:
Frontiers in Neuroscience, Vol 16 (2022)
IntroductionIn the last few years, different studies highlighted a significant enrichment of NEK1 loss of function (LoF) variants in amyotrophic lateral sclerosis (ALS), and an additional role for the p.Arg261His missense variant in the disease susce
Externí odkaz:
https://doaj.org/article/01ce806b8a04474da3c9f08a316db15b
Autor:
Yuri Matteo Falzone, Tommaso Russo, Teuta Domi, Laura Pozzi, Angelo Quattrini, Massimo Filippi, Nilo Riva
Publikováno v:
Neural Regeneration Research, Vol 16, Iss 10, Pp 1985-1991 (2021)
Motor neuron disease includes a heterogeneous group of relentless progressive neurological disorders defined and characterized by the degeneration of motor neurons. Amyotrophic lateral sclerosis is the most common and aggressive form of motor neuron
Externí odkaz:
https://doaj.org/article/3e1e5c39681d4af1b887a8b4e3900f99
Serum naturally occurring anti-TDP-43 auto-antibodies are increased in amyotrophic lateral sclerosis
Autor:
Elisa Conti, Gessica Sala, Susanna Diamanti, Marco Casati, Christian Lunetta, Francesca Gerardi, Claudia Tarlarini, Lorena Mosca, Nilo Riva, Yuri Falzone, Massimo Filippi, Ildebrando Appollonio, Carlo Ferrarese, Lucio Tremolizzo
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-6 (2021)
Abstract Amyotrophic Lateral Sclerosis (ALS) patients express significant clinical heterogeneity that often hinders a correct diagnostic definition. Intracellular deposition of TDP-43, a protein involved in RNA metabolism characterizes the pathology.
Externí odkaz:
https://doaj.org/article/9ef5762f44e5483381b6ff5311429ca6
Autor:
Eleonora Giagnorio, Claudia Malacarne, Paola Cavalcante, Letizia Scandiffio, Marco Cattaneo, Viviana Pensato, Cinzia Gellera, Nilo Riva, Angelo Quattrini, Eleonora Dalla Bella, Giuseppe Lauria, Renato Mantegazza, Silvia Bonanno, Stefania Marcuzzo
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 5, p 4610 (2023)
Amyotrophic lateral sclerosis (ALS) is characterized by the progressive, irreversible loss of upper and lower motor neurons (UMNs, LMNs). MN axonal dysfunctions are emerging as relevant pathogenic events since the early ALS stages. However, the exact
Externí odkaz:
https://doaj.org/article/b8e0f57026df4579a4525a3b24ba198f