Search Results - "Serlenga, L."
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1
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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2
Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis
Published in Neuropathology and applied neurobiology (01-12-2013)“…Aims Sporadic inclusion body myositis (s‐IBM) is characterized by rimmed vacuole formation and misfolded protein accumulation. Intracellular protein aggregates…”
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3
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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4
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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5
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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6
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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7
Classification of amyotrophic lateral sclerosis cases at presentation in epidemiological studies
Published in Neurological sciences (01-12-2005)“…Amyotrophic lateral sclerosis (ALS) diagnosis is based exclusively on clinical grounds because of the absence of biological markers and of specific…”
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8
Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation
Published in Clinical genetics (01-01-2004)Get full text
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Spinocerebellar ataxia type 2 in southern Italy : a clinical and molecular study of 30 families
Published in Journal of neurology (01-06-1999)“…Autosomal dominant cerebellar ataxia type I is the most common form of dominant ataxia. A genetic heterogeneity has been identified with five different loci…”
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10
A randomized controlled trial of recombinant interferon beta-1a in ALS
Published in Neurology (25-01-2000)Get full text
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11
ALS-plus: 5 cases of concomitant amyotrophic lateral sclerosis and parkinsonism
Published in Neurological sciences (01-09-2002)“…According to El Escorial criteria, amyotrophic lateral sclerosis (ALS), combined with other neurologic disorders, such as dementia and parkinsonism, is defined…”
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12
A case of concomitant amyotrophic lateral sclerosis and HIV infection
Published in European journal of neurology (01-03-2002)Get full text
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13
Gravity models of intra-EU trade: application of the CCEP-HT estimation in heterogeneous panels with unobserved common time-specific factors
Published in Journal of applied econometrics (Chichester, England) (01-03-2007)“…We follow recent developments of panel data studies and allow for the existence of both observed and unobserved common factors where their individual responses…”
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14
Mitochondrial disease mimicking polymyositis: a case report
Published in Clinical rheumatology (01-09-2002)“…The authors report on a 34-year-old woman who had developed severe weakness and reduction in grip strength in both upper and lower limbs. Laboratory blood…”
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15
Short-latency median nerve somatosensory evoked potentials in three cases of parkinsonism and dopa responsive dystonia
Published in Functional neurology (01-03-1995)“…We studied somatosensory evoked potentials after median nerve stimulation in a sporadic case of dopa responsive dystonia and in two brothers with different…”
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16
Schwartz-Jampel syndrome with autosomal-dominant inheritance
Published in European neurology (01-01-1982)“…A 4-year follow-up study of 2 brothers affected by Schwartz-Jampel syndrome is reported. The children, aged 16 and 7 years, respectively, showed the clinical…”
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SHORT COMMUNICATION: 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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18
G.P.1 08 Phenotype–genotype correlation in two families with muscle phosphofructokinase deficiency
Published in Neuromuscular disorders : NMD (01-10-2006)Get full text
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Heterogeneity and cross section dependence in panel data models: theory and applications
Published in Journal of applied econometrics (Chichester, England) (01-03-2007)Get full text
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20
Freezing gait in Parkinson's disease
Published in European neurology (01-01-1997)“…Freezing is a well-known problem in Parkinson's disease (PD) and is characterized by an abrupt difficulty in starting or continuing rhythmic and repetitive…”
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