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Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based study

Journal of neurology, neurosurgery and psychiatry, 2008-01, Vol.79 (1), p.33-37

2008

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Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis

Neuropathology and applied neurobiology, 2013-12, Vol.39 (7), p.736-749

2013

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FRI0397 Peculiar expression of autophagy biomarkers in necrotizing autoimmune myopathy muscle

Annals of the rheumatic diseases, 2018-06, Vol.77 (Suppl 2), p.731

2018

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Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis

Neurology, 2008-01, Vol.70 (3), p.222-225

2008

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Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study

Journal of neurology, neurosurgery and psychiatry, 2005-08, Vol.76 (8), p.1094-1098

2005

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Riluzole and amyotrophic lateral sclerosis survival: a population-based study in southern Italy

European journal of neurology, 2007-03, Vol.14 (3), p.262-268

2007

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Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy

European journal of neurology, 2006-07, Vol.13 (7), p.789-792

2006

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Gravity models of intra-EU trade: application of the CCEP-HT estimation in heterogeneous panels with unobserved common time-specific factors

Journal of applied econometrics (Chichester, England), 2007-03, Vol.22 (2), p.361-381

2007

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THU0344 CLINICAL AND HISTOLOGICAL SPECTRUM OF ANTI-MI2 DERMATOMYOSITIS: A MULTICENTRE RETROSPECTIVE COHORT

Annals of the rheumatic diseases, 2020-06, Vol.79 (Suppl 1), p.403-403

2020

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Classification of amyotrophic lateral sclerosis cases at presentation in epidemiological studies

Neurological sciences, 2005-12, Vol.26 (5), p.330-333

2005

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Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation

Clinical genetics, 2004-01, Vol.65 (1), p.64-65

2004

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Spinocerebellar ataxia type 2 in southern Italy : a clinical and molecular study of 30 families

Journal of neurology, 1999-06, Vol.246 (6), p.467-471

1999

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A randomized controlled trial of recombinant interferon beta-1a in ALS

Neurology, 2000-01, Vol.54 (2), p.469-469

2000

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ALS-plus: 5 cases of concomitant amyotrophic lateral sclerosis and parkinsonism

Neurological sciences, 2002-09, Vol.23 Suppl 2, p.S123-s124

2002

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A case of concomitant amyotrophic lateral sclerosis and HIV infection

European journal of neurology, 2002-03, Vol.9 (2), p.180-182

2002

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Mitochondrial disease mimicking polymyositis: a case report

Clinical rheumatology, 2002-09, Vol.21 (5), p.411-414

2002

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SHORT COMMUNICATION: Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy

European journal of neurology, 2006-07, Vol.13 (7), p.789-792

2006

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Freezing gait in Parkinson's disease

European neurology, 1997-01, Vol.38 (4), p.297-301

1997

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G.P.1 08 Phenotype–genotype correlation in two families with muscle phosphofructokinase deficiency

Neuromuscular disorders : NMD, 2006-10, Vol.16 (9), p.656-656

2006

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Heterogeneity and cross section dependence in panel data models: theory and applications

Journal of applied econometrics (Chichester, England), 2007-03, Vol.22 (2), p.229-475

2007

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Short-latency median nerve somatosensory evoked potentials in three cases of parkinsonism and dopa responsive dystonia

Functional neurology, 1995-03, Vol.10 (2), p.99

1995

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Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes

Journal of the neurological sciences, 1996-10, Vol.142 (1-2), p.140-147

1996

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Schwartz-Jampel syndrome with autosomal-dominant inheritance

European neurology, 1982-01, Vol.21 (3), p.137-146

1982

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The epidemiology and treatment of ALS: Focus on the heterogeneity of the disease and critical appraisal of therapeutic trials

Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders, 2011-01, Vol.12 (1), p.1-10

2011

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A randomized controlled trial of recombinant interferon beta-1a in ALS. Italian Amyotrophic Lateral Sclerosis Study Group

Neurology, 2000-01, Vol.54 (2), p.469

2000

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Analysis of survival and prognostic factors in amyotrophic lateral sclerosis: a population based study

Overexpression of autophagic proteins in the skeletal muscle of sporadic inclusion body myositis

FRI0397 Peculiar expression of autophagy biomarkers in necrotizing autoimmune myopathy muscle

Elevated plasma homocysteine levels in patients with amyotrophic lateral sclerosis

Incidence of amyotrophic lateral sclerosis in southern Italy: a population based study

Riluzole and amyotrophic lateral sclerosis survival: a population-based study in southern Italy

Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy

Gravity models of intra-EU trade: application of the CCEP-HT estimation in heterogeneous panels with unobserved common time-specific factors

THU0344 CLINICAL AND HISTOLOGICAL SPECTRUM OF ANTI-MI2 DERMATOMYOSITIS: A MULTICENTRE RETROSPECTIVE COHORT

Classification of amyotrophic lateral sclerosis cases at presentation in epidemiological studies

Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation

Spinocerebellar ataxia type 2 in southern Italy : a clinical and molecular study of 30 families

A randomized controlled trial of recombinant interferon beta-1a in ALS

ALS-plus: 5 cases of concomitant amyotrophic lateral sclerosis and parkinsonism

A case of concomitant amyotrophic lateral sclerosis and HIV infection

Mitochondrial disease mimicking polymyositis: a case report

SHORT COMMUNICATION: Signs and symptoms at diagnosis of amyotrophic lateral sclerosis: a population-based study in southern Italy

Freezing gait in Parkinson's disease

G.P.1 08 Phenotype–genotype correlation in two families with muscle phosphofructokinase deficiency

Heterogeneity and cross section dependence in panel data models: theory and applications

Short-latency median nerve somatosensory evoked potentials in three cases of parkinsonism and dopa responsive dystonia

Autosomal dominant cerebellar ataxia type I. Clinical and molecular study in 36 Italian families including a comparison between SCA1 and SCA2 phenotypes

Schwartz-Jampel syndrome with autosomal-dominant inheritance

The epidemiology and treatment of ALS: Focus on the heterogeneity of the disease and critical appraisal of therapeutic trials

A randomized controlled trial of recombinant interferon beta-1a in ALS. Italian Amyotrophic Lateral Sclerosis Study Group

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