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Nerve ablation after bronchial thermoplasty and sustained improvement in severe asthma

BMC pulmonary medicine, 2018-02, Vol.18 (1), p.29-29, Article 29

2018

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Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Neurology, 2010-08, Vol.75 (7), p.619-625

2010

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Cell-free Protein Synthesis through Solubilisate Exchange in Water/Oil Emulsion Compartments

Chembiochem : a European journal of chemical biology, 2004-08, Vol.5 (8), p.1055-1062

2004

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Mutations in the RYR1 gene in Italian patients at risk for Malignant Hyperthermia: evidence for a cluster of novel mutations in the C-terminal region

Cell calcium (Edinburgh), 2002-09, Vol.32 (3), p.143-151

2002

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Circular dichroic properties and average dimensions of DNA-containing reverse micellar aggregates

Biochimica et biophysica acta, 2002-05, Vol.1562 (1), p.57-62

2002

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Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene

Neurology, 2003-11, Vol.61 (9), p.1288-1291

2003

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Risk of Sporadic Amyotrophic Lateral Sclerosis Associated with Seropositivity for Herpesviruses and Echovirus-7

European journal of epidemiology, 2003-01, Vol.18 (2), p.123-127

2003

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Riluzole and other prognostic factors in ALS: a population-based registry study in Italy

Journal of neurology, 2018-04, Vol.265 (4), p.817-827

2018

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Percutaneous endoscopic gastrostomy, body weight loss and survival in amyotrophic lateral sclerosis: a population-based registry study

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2017-04, Vol.18 (3-4), p.233-242

2017

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A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-08, Vol.16 (5-6), p.331-337

2015

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Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy

Neurological sciences, 2015-12, Vol.36 (12), p.2243-2252

2015

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Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study

European journal of neurology, 2016-09, Vol.23 (9), p.1426-1432

2016

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Recovery from herpes simplex encephalitis: selective impairment of specific semantic categories with neuroradiological correlation

Journal of neurology, neurosurgery and psychiatry, 1988-10, Vol.51 (10), p.1284-1293

1988

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Precocious loss of physiological sleep in a case of Creutzfeldt Jakob disease: a serial polygraphic study

Sleep (New York, N.Y.), 1995-12, Vol.18 (10), p.849-858

1995

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Environmental Exposure to Trace Elements and Risk of Amyotrophic Lateral Sclerosis: A Population-Based Case–Control Study

Environmental research, 2002-06, Vol.89 (2), p.116-123

2002

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Recovery from herpes simplex encephalitis: selective impairment of specific semantic categories with neuroradiological correlation

Neurocase, 1998-08, Vol.4 (4), p.399-427

Pietrini, V.

1998

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Panencephalopathic type of Creutzfeldt-Jakob disease with neuropathologic features similar to Pick's disease

Clinical neuropathology, 1993-01, Vol.12 (1), p.1

1993

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Neuropathy in Tangier disease: A clinicopathologic study and a review of the literature

Acta neurologica Scandinavica, 1985-11, Vol.72 (5), p.495-505

1985

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NEUROPATHOLOGICALLY CONFIRMED SPORADIC CREUTZFELDT-JAKOB DISEASE: INCIDENCE IN AUSTRIA, AND PATTERNS AND DISTRIBUTION OF PRP DEPOSITS IN BRAIN

Journal of neuropathology and experimental neurology, 1996-05, Vol.55 (5), p.661-661

1996

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Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes

Journal of neurology, 1999-05, Vol.246 (5), p.389-393

1999

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Creutzfeldt-Jakob disease presenting as Wernicke-Korsakoff syndrome

Journal of the neurological sciences, 1992-04, Vol.108 (2), p.149-153

Pietrini, Vladimiro

1992

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Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia

Italian journal of neurological sciences, 1998-12, Vol.19 (6), p.345-350

1998

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Acute Confusional Migraine Attacks Resolved by Sleep: Lack of Significant Abnormalities in Post-Ictal Polysomnograms

Cephalalgia, 1986-06, Vol.6 (2), p.95-100

1986

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Anderson-Fabry's disease: neuropathological and neurochemical investigation

Acta neuropathologica, 1982-01, Vol.56 (2), p.93-98

1982

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Tangier neuropathy in Italy

Acta neuropathologica, 1994-10, Vol.88 (4), p.394-395

Pietrini, V

1994

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Nerve ablation after bronchial thermoplasty and sustained improvement in severe asthma

Lithium carbonate in amyotrophic lateral sclerosis: lack of efficacy in a dose-finding trial

Cell-free Protein Synthesis through Solubilisate Exchange in Water/Oil Emulsion Compartments

Mutations in the RYR1 gene in Italian patients at risk for Malignant Hyperthermia: evidence for a cluster of novel mutations in the C-terminal region

Circular dichroic properties and average dimensions of DNA-containing reverse micellar aggregates

Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene

Risk of Sporadic Amyotrophic Lateral Sclerosis Associated with Seropositivity for Herpesviruses and Echovirus-7

Riluzole and other prognostic factors in ALS: a population-based registry study in Italy

Percutaneous endoscopic gastrostomy, body weight loss and survival in amyotrophic lateral sclerosis: a population-based registry study

A further Rasch study confirms that ALSFRS-R does not conform to fundamental measurement requirements

Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy

Amyotrophic lateral sclerosis: a comparison of two staging systems in a population-based study

Recovery from herpes simplex encephalitis: selective impairment of specific semantic categories with neuroradiological correlation

Precocious loss of physiological sleep in a case of Creutzfeldt Jakob disease: a serial polygraphic study

Environmental Exposure to Trace Elements and Risk of Amyotrophic Lateral Sclerosis: A Population-Based Case–Control Study

Recovery from herpes simplex encephalitis: selective impairment of specific semantic categories with neuroradiological correlation

Panencephalopathic type of Creutzfeldt-Jakob disease with neuropathologic features similar to Pick's disease

Neuropathy in Tangier disease: A clinicopathologic study and a review of the literature

NEUROPATHOLOGICALLY CONFIRMED SPORADIC CREUTZFELDT-JAKOB DISEASE: INCIDENCE IN AUSTRIA, AND PATTERNS AND DISTRIBUTION OF PRP DEPOSITS IN BRAIN

Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes

Creutzfeldt-Jakob disease presenting as Wernicke-Korsakoff syndrome

Clinical and genetic study of a family with spinocerebellar ataxia type 1 (SCA1) and beta-thalassemia

Acute Confusional Migraine Attacks Resolved by Sleep: Lack of Significant Abnormalities in Post-Ictal Polysomnograms

Anderson-Fabry's disease: neuropathological and neurochemical investigation

Tangier neuropathy in Italy

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