-
Article
Open AccessUniversal Prevention of Dementia in Italy: A Document Analysis of the 21 Italian Regional Prevention Plans
Up to 40% of dementia cases are theoretically avoidable and population-level interventions (i.e., universal prevention) are a key component in facing the global public health challenge of dementia. However, in...
-
Article
Open AccessA systematic review on the risk of neurodegenerative diseases and neurocognitive disorders in professional and varsity athletes
The aim of this systematic review (SR) was to gather all available epidemiological evidence on former participation in any type of sport, at a professional and varsity level, as a potential risk factor for neu...
-
Chapter and Conference Paper
Instrumented Balance and Gait Assessment in Patients with Charcot-Marie-Tooth Peripheral Neuropathy
Gait and balance deficits are major impairments for Charcot-Marie-Tooth 1A (CMT1A) patients. However, motor rehabilitation is a challenge in CMT1A patients. There are poor evidences of clinical efficacy and lo...
-
Article
Open Access5th National Congress of the Italian Society of Physiotherapy
S1 Criteria for exercises selection in subjects with low back pain
-
Article
Erratum to: Exploring motor and visual imagery in Amyotrophic Lateral Sclerosis
-
Article
Exploring motor and visual imagery in Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis (ALS) is a motor neuron disease characterized by the progressive atrophy of both the first and the second motor neurons. Although the cognitive profile of ALS patients has already...
-
Article
Open AccessThe MEG detector for μ +→e+ γ decay search
The MEG (Mu to Electron Gamma) experiment has been running at the Paul Scherrer Institut (PSI), Switzerland since 2008 to search for the decay μ +→e+ γ by using one of the most int...
-
Article
Open AccessSearch for the Higgs boson in the all-hadronic final state using the full CDF data set
This paper reports the result of a search for the standard model Higgs boson in events containing four reconstructed jets associated with quarks. For masses below 135 GeV/c 2, the Higgs bo...
-
Article
Open AccessSearch for scalar top quark production in \( p\bar{p} \) collisions at \( \sqrt{s}=1.96\;\mathrm{TeV} \)
We report on a search for the supersymmetric partner of the top quark (scalar top) decaying into a charm quark and a neutralino in $ p\bar{p} ...
-
Article
Open AccessImproved determination of the sample composition of dimuon events produced in \(p\bar{p}\) collisions at \(\sqrt{s}=1.96\) TeV
We use a new method to estimate with 5% accuracy the contribution of pion and kaon in-flight-decays to the dimuon data set acquired with the CDF detector. Based on this improved estimate, we show that the tota...
-
Article
Stochastic modelling of apoptosis kinetics
Robust quantitative estimation of average whole cell mitochondrial dysfunction is a useful tool for assessing sensitivity to apoptotic stimuli induced either by novel agents, or following manipulation of apopt...
-
Article
Open AccessBcl-2 resistant mitochondrial toxicity mediated by the isoquinoline carboxamide PK11195 involves de novo generation of reactive oxygen species
Resistance to apoptosis is a major obstacle preventing effective therapy for malignancy. Mitochondria localized anti-death proteins of the Bcl-2 family play a central role in inhibiting apoptosis and therefore...
-
Article
Intravascular malignant lymphomatosis with neurological symptoms
-
Article
Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
-
Article
Cryoglobulinemic neuropathy: case report
We report the case of a 51-year-old man affected by mainly motor polyneuropathy with subacute onset and tendency to chronicization. Several possible etiological factors were present, but nerve biopsy, showing ...
-
Article
Recurrent familial neuropathy due to liability to pressure palsies
Two families with hereditary neuropathy with liability to pressure palsies (HNPP) were evaluated clinically, electrophysiologically and pathologically (2 index cases). Familial patterns suggest autosomal domin...
-
Article
Hereditary motor neuropathy, distal type: electrophysiological and pathological studies of a case
A case of HMN, distal type transmitted as autosomal dominant is described. Clinical findings appear to be consistent with a peroneal muscular atrophy, indistinguishable from HMSN types I and II. The electrophy...
