Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Elio Lugaresi"'
Autor:
Margherita Fabbri, Piero Parchi, Paolo Tinuper, Pietro Cortelli, Giovanna Calandra-Buonaura, Elio Lugaresi, Sabina Capellari
Publikováno v:
Movement Disorders. 29:420-424
Background Fatal familial insomnia (FFI) is a hereditary autosomal-dominant prion disease linked to a mutation of the prion protein gene and characterized by sleep and autonomic abnormalities at onset followed by motor disturbances. We describe gait
Publikováno v:
Acta Neurologica Scandinavica. 81:113-117
We studied clinically and electrophysiologically 8 patients affected by ortho-static tremor (OT), which is an unusual movement disorder consisting of shaking movements of the legs and trunk in the standing position. We failed to find any cause in 6 o
Publikováno v:
Acta Neurologica Scandinavica. 71:498-503
– Two cases of X-linked bulbo-spinal neuronopathy (BSN) of late onset are presented. An extensive review of the literature shows that, in addition to the signs of a chronic degeneration of brainstem and spinal neurons, other clinical features may a
Publikováno v:
Revue Neurologique. 164:692-700
Fatal familial insomnia, a human prion disease, Morvan's chorea, an autoimmune limbic encephalopathy, and delirium tremens, the well-known alcohol (or benzodiazepine [BDZ]) withdrawal syndrome, share a clinical phenotype largely consisting in an inab
Publikováno v:
Movement Disorders. 23:858-865
Cataplexy, the hallmark of narcolepsy, has been well characterized in adults but not in children. This study systematically used structured clinical assessments and video-recordings (49 episodes in eight cases) to evaluate cataplexy in 23 patients di
Autor:
Federica Provini, Roberto D'Angelo, Pasquale Montagna, Roberto Vetrugno, Giuseppe Plazzi, Elio Lugaresi
Publikováno v:
European Journal of Neurology. 14:1236-1243
Catathrenia (nocturnal groaning) is a rare condition characterized by monotonous irregular groans occurring during sleep. Ten patients (five women; mean age: 27 +/- 7.4 years, range: 15-41) with sleep-related groaning persisting for years or decades
Autor:
Elio Lugaresi, Federica Provini
Publikováno v:
Sleep Medicine ISBN: 9781493920884
In 1986, we described a novel disease named fatal familial insomnia (FFI) in which selective atrophy of the anterior and medio-dorsal thalamic nuclei led to a progressive loss of the ability to sleep, associated with apathy and motor and autonomic ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4c5e3c19d7260ab398e9a968002ff5d
https://doi.org/10.1007/978-1-4939-2089-1_34
https://doi.org/10.1007/978-1-4939-2089-1_34
Publikováno v:
Brain Pathol
The key clinical aspects of FFI, i.e. hypovigilance and attention deficit, inability to generate EEG sleep patterns, sympathetic hyperactivity and attenuation of vegetative and hormonal circadian oscillations, are related to selective atrophy of the
Publikováno v:
The Lancet Neurology. 2:167-176
Familial fatal insomnia (FFI)--a hereditary prion disease caused by a mutation at codon 178 of the prion-protein (PrP) gene (PRNP) that leads to a D178N substitution in the protein--and its sporadic form, sporadic fatal insomnia (SFI), have similar d
Publikováno v:
Europe PubMed Central
We describe a polysomnographic observation of the acute phase of the alcohol withdrawal syndrome, characterized by an alteration of the sleep–wake cycle and by the absence of non-rapid eye movement sleep. An atypical transitional state between rapi