Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Luca eGuglielmi"'
Autor:
Maria Cristina D'Adamo, Sonia eHasan, Luca eGuglielmi, Ilenio eServettini, Marta eCenciarini, Luigi eCatacuzzeno, Fabio eFranciolini
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
Episodic ataxia type 1 (EA1) is a K+ channelopathy characterized by a broad spectrum of symptoms. Generally, patients may experience constant myokymia and dramatic episodes of spastic contractions of the skeletal muscles of the head, arms, and legs w
Externí odkaz:
https://doaj.org/article/29c10edcbd1449f68fcc65e14f91aeba
Autor:
Luigi eCatacuzzeno, Martino eCaramia, Luigi eSforna, Silvia eBelia, Luca eGuglielmi, Maria Cristina D'Adamo, Mauro ePessia, Fabio eFranciolini
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
Glioblastoma is the most common and aggressive primary brain tumor, and is notable for spreading so effectively through the brain parenchyma to make complete surgical resection virtually impossible, and prospect of life dismal. Several ion channels h
Externí odkaz:
https://doaj.org/article/98159cc16ce14817b3bdd0bd614fa72e
Autor:
Luca eGuglielmi, Ilenio eServettini, Martino eCaramia, Luigi eCatacuzzeno, Fabio eFranciolini, Maria Cristina D'Adamo, Mauro ePessia
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 9 (2015)
Autism spectrum disorders (ASDs) are characterized by impaired ability to properly implement environmental stimuli that are essential to achieve a state of social and cultural exchange. Indeed, the main features of ASD are impairments of interpersona
Externí odkaz:
https://doaj.org/article/9be386f54bc04786a6fe9cd66ed306cb
Autor:
Maria Cristina D'Adamo, Constanze eGallenmueller, Ilenio eServettini, Elisabeth eHartl, Stephen eTucker, Larissa eArning, Saskia eBiskup, Alessandro eGrottesi, Luca eGuglielmi, Paola eImbrici, Pia eBernasconi, Giuseppe eDi Giovanni, Fabio eFranciolini, Luigi eCatacuzzeno, Mauro ePessia, Thomas eKlopstock
Publikováno v:
Frontiers in Physiology, Vol 5 (2015)
Episodic ataxia type 1 (EA1) is an autosomal dominant K+ channelopathy which manifests with short attacks of cerebellar ataxia and dysarthria, and may also show interictal myokymia. Episodes can be triggered by emotional or physical stress, startle r
Externí odkaz:
https://doaj.org/article/3eb82c1e96d74d0d8f838a1bf0916eb4