Search Results - "Monza, D"
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1
Whole body cholesterol metabolism is impaired in Huntington's disease
Published in Neuroscience letters (02-05-2011)“…► Impaired cholesterol biosynthesis in rodent models of Huntington Disease (HD). ► Reduced brain cholesterol turnover in HD patients as plasma…”
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2
Cognitive and magnetic resonance imaging aspects of corticobasal degeneration and progressive supranuclear palsy
Published in Neurology (11-08-1999)“…To identify cognitive and MRI features important for the clinical diagnosis of corticobasal degeneration (CBD) and progressive supranuclear palsy (PSP); these…”
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3
Neuropsychological follow up in patients with Parkinson's disease, striatonigral degeneration-type multisystem atrophy, and progressive supranuclear palsy
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2000)“…OBJECTIVES Impairment of executive function is frequent in Parkinson's disease (PD), striatonigral degeneration-type multisystem atrophy (SND), and progressive…”
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4
Affective symptoms in multiple system atrophy and Parkinson’s disease: response to levodopa therapy
Published in Journal of neurology, neurosurgery and psychiatry (01-04-1999)“…The objective was to determine the extent to which psychiatric disturbances (especially mood disorders) generally considered poor prognostic factors, are…”
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5
Comparison of natural histories of progressive supranuclear palsy and multiple system atrophy
Published in Neurological sciences (01-06-2001)“…In order to identify early clinical features and survival predictors of supranuclear palsy (PSP) and multiple system atrophy (MSA), we compared the disease…”
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6
Neurophysiological features in relation to clinical signs in clinically diagnosed corticobasal degeneration
Published in Neurological sciences (01-04-2003)“…We investigated the association between clinical and neurophysiological characteristics in patients with a clinical diagnosis of probable corticobasal…”
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7
Cognitive and psychiatric characterization of patients with Huntington's disease and their at-risk relatives
Published in Neurological sciences (01-09-2002)“…We examined cognitive and psychiatric disturbances in patients with Huntington's disease (HD) in comparison to at-risk asymptomatic subjects. Cognitive and…”
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8
A study of arm movements in Huntington's disease under visually controlled and blindfolded conditions
Published in Neurological sciences (01-02-2003)“…The so-called bradykinesia of Huntington's disease (HD) seems not due to reduced movement speed alone but may also be task-dependent. We therefore investigated…”
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9
Progression of motor and cognitive impairment in Parkinson's disease
Published in Journal of neurology (01-08-1995)“…We performed a longitudinal study (mean follow-up 86.7 months) to evaluate motor and mental deterioration in patients with Parkinson's disease. Of the original…”
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10
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY
Published in Journal of neurology, neurosurgery and psychiatry (01-12-2011)Get full text
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11
Identification of symbol digit modality test score extremes in Huntington's disease
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (01-04-2019)“…Studying individuals with extreme phenotypes could facilitate the understanding of disease modification by genetic or environmental factors. Our aim was to…”
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12
Variations in axial, proximal, and distal motor response to L-dopa in multisystem atrophy and Parkinson's disease
Published in Clinical neuropharmacology (01-06-1997)“…The purpose of this study was to quantitatively compare the motor response to L-dopa in Parkinson's disease (PD) and striatonigral-type multisystem atrophy…”
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13
Cognitive dysfunction and impaired organization of complex motility in degenerative parkinsonian syndromes
Published in Archives of neurology (Chicago) (01-03-1998)“…A frontostriatal pattern of cognitive decline, consisting of a frontal lobe-like syndrome without genuine cortical defects such as amnesia, apraxia, aphasia,…”
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14
G07 Differences between Huntington's disease and spinocerebellar ataxia types 1 and 2 on cognitive and behavioural profile
Published in Journal of neurology, neurosurgery and psychiatry (01-09-2010)“…Background Huntington's disease (HD) patients show progressive, mostly frontal-striatal-type, cognitive deterioration, and heterogeneous psychiatric symptoms…”
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15
Corrigendum to “Whole body cholesterol metabolism is impaired in Huntington's disease” [Neurosci. Lett. 494 (2011) 245–249]
Published in Neuroscience letters (08-07-2011)Get full text
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16
Psychiatric symptoms do not correlate with cognitive decline, motor symptoms, or CAG repeat length in Huntington's disease
Published in Archives of neurology (Chicago) (01-06-1996)“…To investigate the hypothesis that psychiatric disturbances in Huntington's disease are related to degree of cognitive or motor compromise and to determine…”
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17
Cognitive and MRI aspects of corticobasal degeneration and progressive supranuclear palsy
Published in Neurology (09-05-2000)Get full text
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18
Hemiballism in a patient with probable multiple system atrophy
Published in Functional neurology (01-01-1997)“…We report a patient with long-standing asymmetrical parkinsonism, cerebellar ataxia and dysautonomia, suggestive of multiple system atrophy (MSA). However, the…”
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Combined poly(isobutylcyanoacrylate) and cyclodextrins nanoparticles for enhancing the encapsulation of lipophilic drugs
Published in Pharmaceutical research (01-07-1998)“…The aim of this study was to prepare and characterize nanoparticulate systems constituted of poly(isobutylcyanoacrylate) and cyclodextrins and intended for…”
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A case of dementia parkinsonism resembling progressive supranuclear palsy due to mutation in the tau protein gene
Published in Archives of neurology (Chicago) (01-10-2003)“…Few cases of frontotemporal dementia parkinsonism (FTDP-17) have been described in the literature. To our knowledge, this is the first Italian case. To report…”
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