Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Alex, Incensi"'
Autor:
Alessandro Furia, Raffaello Ditaranto, Elena Biagini, Vanda Parisi, Alex Incensi, Sara Parisini, Rocco Liguori, Vincenzo Donadio
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-5 (2024)
Abstract Background Fabry disease is a multisystemic disorder characterized by deposition of globotriaosylceramide (Gb3) and its deacylated form in multiple organs, sometimes localized in specific systems such as the nervous or cardiovascular system.
Externí odkaz:
https://doaj.org/article/3d04e2c9565448a3adf228532aa4bf2c
Autor:
Irene Simonetta, Renata Riolo, Federica Todaro, Vincenzo Donadio, Alex Incensi, Salvatore Miceli, Paolo Colomba, Giovanni Duro, Antonino Tuttolomondo
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/c484d23f8b7247efa94004343fba4687
Autor:
Irene Simonetta, Renata Riolo, Federica Todaro, Vincenzo Donadio, Alex Incensi, Salvatore Miceli, Paolo Colomba, Giovanni Duro, Antonino Tuttolomondo
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Background: Anderson–Fabry disease (AFD) is an X-linked disease that results from reduced activity of the enzyme galactosidase alpha (GLA). When the GLA gene sequence is altered by mutations that alter the normal DNA sequence, variants of the alpha
Externí odkaz:
https://doaj.org/article/33ade6485def44aeb5ff52fc177b417a
Autor:
Elena Antelmi, Fabio Pizza, Vincenzo Donadio, Marco Filardi, Yuri L. Sosero, Alex Incensi, Stefano Vandi, Monica Moresco, Raffaele Ferri, Sara Marelli, Luigi Ferini‐Strambi, Rocco Liguori, Giuseppe Plazzi
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 9, Pp 1872-1876 (2019)
Abstract To search for discriminating biomarkers, 30 patients with idiopathic rapid‐eye‐movements sleep behavior disorder (iRBD) were compared with 17 patients with RBD within narcolepsy type 1. Both groups underwent extensive examinations, inclu
Externí odkaz:
https://doaj.org/article/795d386bb8824d61ac655fc5aaaf5298
Autor:
Vincenzo Donadio, Alex Incensi, Giovanni Rizzo, Gunilla T Westermark, Grazia Devigili, Rosa De Micco, Alessandro Tessitore, Dag Nyholm, Sara Parisini, Dag Nyman, Gioacchino Tedeschi, Roberto Eleopra, Martin Ingelsson, Rocco Liguori
Publikováno v:
Brain. 146:1065-1074
Multiple system atrophy (MSA) is characterized by accumulation of phosphorylated α-synuclein (p-syn) as glial cytoplasmic inclusions in the brain and a specific biomarker for this disorder is urgently needed. We aimed at investigating if p-syn can a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39d68677af175c4d149407527a2661a
https://doi.org/10.1093/brain/awac124
https://doi.org/10.1093/brain/awac124
Autor:
Matteo Foschi, Veria Vacchiano, Patrizia Avoni, Alex Incensi, Stella Battaglia, Vincenzo Donadio, Elena Panzeri, Maria Teresa Bassi, Rocco Liguori, Giovanni Rizzo
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
X-linked adrenoleukodystrophy (x-ALD) is a rare genetic disorder caused by a mutation in the ABCD1 gene, which encodes for a peroxisomal very long chain fatty acid transporter. Clinically, x-ALD can present a wide spectrum of different phenotypes: as
Externí odkaz:
https://doaj.org/article/10a18874999c45508e9c54dee3c02c60
Autor:
Tommaso Pippucci, Alessandra Maresca, Pamela Magini, Giovanna Cenacchi, Vincenzo Donadio, Flavia Palombo, Valentina Papa, Alex Incensi, Giuseppe Gasparre, Maria Lucia Valentino, Carmela Preziuso, Annalinda Pisano, Michele Ragno, Rocco Liguori, Carla Giordano, Caterina Tonon, Raffaele Lodi, Antonia Parmeggiani, Valerio Carelli, Marco Seri
Publikováno v:
EMBO Molecular Medicine, Vol 7, Iss 6, Pp 848-858 (2015)
Abstract Notch signaling is essential for vascular physiology. Neomorphic heterozygous mutations in NOTCH3, one of the four human NOTCH receptors, cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADAS
Externí odkaz:
https://doaj.org/article/420851423e1b455bab5ab25116d4ca8c
Autor:
Vincenzo Donadio, Alex Incensi, Giovanni Rizzo, Enrico Fileccia, Francesco Ventruto, Antonella Riva, Domenico Tiso, Martino Recchia, Veria Vacchiano, Rossella Infante, Giovanna Petrangolini, Pietro Allegrini, Silvia Avino, Roberta Pantieri, Barbara Mostacci, Patrizia Avoni, Rocco Liguori
There are currently no standardized therapies for Parkinson disease (PD). Curcumin shows anti-amyloidogenic properties in vitro and may be a promising treatment for PD. We evaluated the effects of curcumin supplementation on clinical scales and misfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e646409de3740fb5459e36b0f438f179
https://hdl.handle.net/11585/897697
https://hdl.handle.net/11585/897697
Autor:
Alex Incensi, Rocco Liguori, E. Fileccia, Damiano Galimberti, Vincenzo Donadio, Fabrizio Salvi, Giacomo Rao, Francesco Ventruto, Giovanni Rizzo
Publikováno v:
Journal of Neuropathology & Experimental Neurology. 80:868-874
Small fiber neuropathy (SFN) is characterized by the involvement of Aδ and C fibers leading to sensory, mainly pain, and/or autonomic symptoms. Multiple chemical sensitivity syndrome (MCS) is an incompletely defined condition characterized by the on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b144763093c76dc1b17f4982332b63ac
https://doi.org/10.1093/jnen/nlab082
https://doi.org/10.1093/jnen/nlab082
Autor:
Rocco Liguori, Alex Incensi, Silvia de Pasqua, Renzo Mignani, Enrico Fileccia, Marisa Santostefano, Elena Biagini, Claudio Rapezzi, Silvia Palmieri, Ilaria Romani, Walter Borsini, Alessandro Burlina, Roberto Bombardi, Marco Caprini, Patrizia Avoni, Vincenzo Donadio
Publikováno v:
PLoS ONE, Vol 12, Iss 7, p e0180581 (2017)
Fabry Disease (FD) is characterized by globotriaosylceramide-3 (Gb3) accumulation in several tissues and a small fibre neuropathy (SFN), however the underlying mechanisms are poorly known. This study aimed to: 1) ascertain the presence of Gb3 deposit
Externí odkaz:
https://doaj.org/article/ffa3ab7f4802476980d29491895ea22c