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Definition of fibromyalgia severity: findings from a cross-sectional survey of 2339 Italian patients

Rheumatology (Oxford, England), 2021-02, Vol.60 (2), p.728-736

2021

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Measuring multimorbidity inequality across Italy through the multisource comorbidity score: a nationwide study

European journal of public health, 2020-10, Vol.30 (5), p.916-921

2020

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Cost-effectiveness of the adherence with recommendations for clinical monitoring of patients with diabetes

Nutrition, metabolism, and cardiovascular diseases, 2021-10, Vol.31 (11), p.3111-3121

2021

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Mangostanin, a Xanthone Derived from Garcinia mangostana Fruit, Exerts Protective and Reparative Effects on Oxidative Damage in Human Keratinocytes

Pharmaceuticals (Basel, Switzerland), 2022-01, Vol.15 (1), p.84

2022

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Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene

International journal of molecular sciences, 2022-09, Vol.23 (18), p.10210

2022

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Dibutyryl cAMP- or Interleukin-6-induced astrocytic differentiation enhances mannose binding lectin (MBL)-associated serine protease (MASP)-1/3 expression in C6 glioma cells

Archives of biochemistry and biophysics, 2018-09, Vol.653, p.39-49

2018

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Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt‐Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma

Neuropathology, 2017-04, Vol.37 (2), p.110-115

2017

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A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease

Annals of neurology, 1993-12, Vol.34 (6), p.802-807

1993

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Methylenetetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms in two genetically and diagnostically distinct cohort of Alzheimer patients

Neurobiology of aging, 2003-11, Vol.24 (7), p.933-939

2003

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Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation

Nature (London), 1992-04, Vol.356 (6370), p.598-601

1992

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N-Terminal Domain of 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase Harbors a GTP/ATP Binding Site

Chemical biology & drug design, 2007-12, Vol.70 (6), p.502-510

2007

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Performance Evaluation for a HTS Transformer

IEEE transactions on applied superconductivity, 2006-06, Vol.16 (2), p.1501-1504

2006

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Polymorphisms of the Prion Protein gene in Italian patients with Creutzfeldt-Jakob disease

Human genetics, 1994-10, Vol.94 (4), p.375-379

1994

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Survival in Alzheimer's disease is shorter in women carrying heterozygosity at codon 129 of the PRNP gene and no APOE epsilon 4 allele

Dementia and geriatric cognitive disorders, 2008, Vol.25 (4), p.354

2008

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Sulphate polyanions prolong the incubation period of scrapie-infected hamsters

Journal of general virology, 1992-03, Vol.73 (3), p.661-665

1992

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Research Article: The N-Terminal Domain of 2′,3′-Cyclic Nucleotide 3′-Phosphodiesterase Harbors a GTP/ATP Binding Site

Chemical biology & drug design, 2007-12, Vol.70 (6), p.502-510

2007

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Amphotericin B Delays the Incubation Period of Scrapie in Intracerebrally Inoculated Hamsters

Journal of general virology, 1987-01, Vol.68 (1), p.219-223

1987

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Failure to ameliorate Creutzfeldt-Jakob disease with amphotericin B therapy

The Journal of infectious diseases, 1992-04, Vol.165 (4), p.784

1992

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Creutzfeldt-Jakob disease after non-commercial dura mater graft

The Lancet (British edition), 1992-09, Vol.340 (8819), p.614-615

1992

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Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Gene a: DELETION OF PrP GENE IN DEMENTIA

Annals of the New York Academy of Sciences, 1994-05, Vol.724 (1), p.358-360

1994

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Data acquisition electronics for NESTOR experiment: project and tests

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 1999-02, Vol.423 (1), p.146-156

1999

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Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Genea

Annals of the New York Academy of Sciences, 1994-05, Vol.724 (1), p.358-360

1994

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Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Gene

Annals of the New York Academy of Sciences, 1994-06, Vol.724 (1), p.358-360

1994

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Polymorphisms of the Prion Protein gene in italian patients with Creutzfeldt-Jakob disease

Human genetics, 1995-05, Vol.95 (5)

1995

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Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma

Neuropathology : official journal of the Japanese Society of Neuropathology, 2017, Vol.37 (2), p.110-115

2017

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Definition of fibromyalgia severity: findings from a cross-sectional survey of 2339 Italian patients

Measuring multimorbidity inequality across Italy through the multisource comorbidity score: a nationwide study

Cost-effectiveness of the adherence with recommendations for clinical monitoring of patients with diabetes

Mangostanin, a Xanthone Derived from Garcinia mangostana Fruit, Exerts Protective and Reparative Effects on Oxidative Damage in Human Keratinocytes

Biochemical and Neuropathological Findings in a Creutzfeldt–Jakob Disease Patient with the Rare Val180Ile-129Val Haplotype in the Prion Protein Gene

Dibutyryl cAMP- or Interleukin-6-induced astrocytic differentiation enhances mannose binding lectin (MBL)-associated serine protease (MASP)-1/3 expression in C6 glioma cells

Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt‐Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease

Methylenetetrahydrofolate reductase and angiotensin converting enzyme gene polymorphisms in two genetically and diagnostically distinct cohort of Alzheimer patients

Amphotericin B treatment dissociates in vivo replication of the scrapie agent from PrP accumulation

N-Terminal Domain of 2',3'-Cyclic Nucleotide 3'-Phosphodiesterase Harbors a GTP/ATP Binding Site

Performance Evaluation for a HTS Transformer

Polymorphisms of the Prion Protein gene in Italian patients with Creutzfeldt-Jakob disease

Survival in Alzheimer's disease is shorter in women carrying heterozygosity at codon 129 of the PRNP gene and no APOE epsilon 4 allele

Sulphate polyanions prolong the incubation period of scrapie-infected hamsters

Research Article: The N-Terminal Domain of 2′,3′-Cyclic Nucleotide 3′-Phosphodiesterase Harbors a GTP/ATP Binding Site

Amphotericin B Delays the Incubation Period of Scrapie in Intracerebrally Inoculated Hamsters

Failure to ameliorate Creutzfeldt-Jakob disease with amphotericin B therapy

Creutzfeldt-Jakob disease after non-commercial dura mater graft

Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Gene a: DELETION OF PrP GENE IN DEMENTIA

Data acquisition electronics for NESTOR experiment: project and tests

Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Genea

Progressive Dementia in a Young Patient with a Homozygous Deletion of the PrP Gene

Polymorphisms of the Prion Protein gene in italian patients with Creutzfeldt-Jakob disease

Patient with rapidly evolving neurological disease with neuropathological lesions of Creutzfeldt-Jakob disease, Lewy body dementia, chronic subcortical vascular encephalopathy and meningothelial meningioma

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