Search Results - "ZOCCOLELLA, S"
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Clinical Profiles and Patterns of Neurodegeneration in Amyotrophic Lateral Sclerosis: A Cluster-Based Approach Based on MR Imaging Metrics
Published in American journal of neuroradiology : AJNR (01-04-2023)“…The previous studies described phenotype-associated imaging findings in amyotrophic lateral sclerosis (ALS) with a prior categorization of patients based on…”
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Elevated cerebrospinal fluid neurofilament light levels in patients with amyotrophic lateral sclerosis: a possible marker of disease severity and progression
Published in European journal of neurology (01-12-2012)“…Background To date there are no biomarkers with proven reliability as a measure of disease burden in amyotrophic lateral sclerosis (ALS). The aim of our study…”
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3
A 71‐nucleotide deletion in the periaxin gene in an Italian patient with late‐onset slowly progressive demyelinating Charcot‐Marie‐Tooth disease
Published in European journal of neurology (01-10-2020)“…Background Charcot‐Marie‐Tooth disease (CMT) constitutes a group of heterogeneous hereditary motor and sensor neuropathies. Mutations in the periaxin (PRX)…”
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Cerebrospinal fluid neurofilament light chain levels: marker of progression to generalized amyotrophic lateral sclerosis
Published in European journal of neurology (01-01-2015)“…Background and purpose To evaluate whether cerebrospinal fluid (CSF) neurofilament light chain (NFL) levels could predict the time to generalization (TTG) in…”
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Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based study
Published in Journal of neurology, neurosurgery and psychiatry (01-01-2008)“…Objective:To measure survivorship and predictors of prognosis of amyotrophic lateral sclerosis (ALS).Methods:Incident cases, diagnosed in the 1998–1999 period…”
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6
Lymphocyte subsets as biomarkers of therapeutic response in Fingolimod treated Relapsing Multiple Sclerosis patients
Published in Journal of neuroimmunology (15-02-2017)“…Abstract We investigated, lymphocyte count (LC) and lymphocyte subsets (LS ) in a real life setting of Fingolimod (FTY) treated Relapsing MS (RMS) patients …”
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7
Time to generalization and prediction of survival in patients with amyotrophic lateral sclerosis: a retrospective observational study
Published in European journal of neurology (01-06-2016)“…Background and purpose A strong association between time to generalization (TTG), considered as the time of spreading of the clinical signs from spinal or…”
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8
Trauma and amyotrophic lateral sclerosis: a case-control study from a population-based registry
Published in European journal of neurology (01-12-2012)“…Background and purpose Published reports on the association between amyotrophic lateral sclerosis (ALS) and trauma are controversial suggesting the need for a…”
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Elevated homocysteine levels in Parkinson's Disease: is there anything besides L-dopa treatment?
Published in Current medicinal chemistry (2010)“…Homocysteine (Hcy) exerts multiple neurotoxic mechanisms that have been linked to the pathogenesis of neurodegenerative disorders. Several studies observed…”
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Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis
Published in Neurology (15-01-2008)“…Both in vitro and in vivo studies indicate that homocysteine (Hcy) may be directly involved in the damage of motor neurons and in several pathways implicated…”
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11
Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study
Published in Journal of neurology, neurosurgery and psychiatry (01-08-2005)“…Background: While the incidence of amyotrophic lateral sclerosis (ALS) is similar across the world (range, 1.0 to 2.5/100 000), a latitude gradient from north…”
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12
Riluzole and amyotrophic lateral sclerosis survival: a population-based study in southern Italy
Published in European journal of neurology (01-03-2007)“…Riluzole is to date the only treatment that prolongs amyotrophic lateral sclerosis (ALS) survival. However, results on the efficacy of riluzole in…”
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13
Cerebrospinal fluid neurofilament tracks fMRI correlates of attention at the first attack of multiple sclerosis
Published in Multiple sclerosis (01-04-2015)“…Background: Identifying markers of cognitive dysfunction in multiple sclerosis (MS) is extremely challenging since it means supplying potential biomarkers for…”
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Hyperhomocysteinemia in L-dopa treated patients with Parkinson's disease: potential implications in cognitive dysfunction and dementia?
Published in Current medicinal chemistry (01-09-2010)“…Hyperhomocysteinemia has been associated with cognitive dysfunction and dementia. The incidence of dementia in Parkinson's Disease (PD) patients is higher than…”
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15
Load-dependent dysfunction of the putamen during attentional processing in patients with clinically isolated syndrome suggestive of multiple sclerosis
Published in Multiple sclerosis (01-08-2013)“…Background: Load-related functional magnetic resonance imaging (fMRI) abnormalities of brain activity during performance of attention tasks have been described…”
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72. Electromiography as useful test in the differential diagnosis of neuromuscular diseases only after clinical examination
Published in Clinical neurophysiology (01-11-2013)“…Electromiography (EMG) plays a key role in the evaluation of patients with neuromuscular diseases. It can be considered an extension of the neurological…”
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The incidence of major stroke subtypes in Southern Italy: a population-based study
Published in European journal of neurology (01-09-2010)“…Background and purpose: Stroke is characterized by well‐defined clinical major subtypes, but there are few studies on incidence rates, aetiologies and…”
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18
Mitochondrial genome large rearrangements in the skeletal muscle of a patient with PMA
Published in European journal of neurology (01-07-2012)Get full text
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Concomitant myotonic dystrophy type 1, CIDP-like neuropathy and Hashimoto thyroiditis: a causal link?
Published in European journal of neurology (01-10-2012)Get full text
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Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy
Published in European journal of neurology (01-07-2006)“…Amyotrophic lateral sclerosis (ALS) diagnostic criteria are used to select patients for clinical trials based on different levels of diagnostic certainty,…”
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