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Survey on antimicrobial prescribing patterns in small animal veterinary practice in Emilia Romagna, Italy

Veterinary record, 2017-07, Vol.181 (3), p.69-69

2017

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RAPID EMERGENCE OF CANDIDA AURIS IN NORTH ITALY, 2019 TO JULY 2022

International journal of infectious diseases, 2023-05, Vol.130, p.S130-S131

2023

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Depletion study of PCDD/Fs and dioxin-like PCBs concentrations in contaminated home-produced eggs: Preliminary study

Analytica chimica acta, 2010-07, Vol.672 (1), p.50-54

2010

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Management of vaccine-related issues during a pandemic emergency: activation of a referral center

European journal of public health, 2022-10, Vol.32 (Supplement_3)

2022

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Decrease in Hospital Admissions for Transient Ischemic Attack, Mild, and Moderate Stroke During the COVID-19 Era

Stroke (1970), 2020-08, Vol.51 (8), p.2315-2321

2020

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Giant Retroperitoneal Myelolipoma: An Unusual Diagnostic GI Challenge—Case Report and Review of the Literature

Digestive diseases and sciences, 2019-12, Vol.64 (12), p.3431-3435

2019

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A novel AβPP mutation exclusively associated with cerebral amyloid angiopathy

Annals of neurology, 2005-10, Vol.58 (4), p.639-644

2005

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Proceedings of the 29th ISFG Congress

Forensic science international. Genetics supplement series, 2022-12, Vol.8, p.1-2

2022

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Analysis of Vλ-Jλ expression in plasma cells from primary (AL) amyloidosis and normal bone marrow identifies 3r(λIII) as a new amyloid-associated germline gene segment

Blood, 2002-08, Vol.100 (3), p.948-953

2002

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When Should Cardiologists Suspect Anderson-Fabry Disease?

The American journal of cardiology, 2010-11, Vol.106 (10), p.1492-1499

2010

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Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy

The American journal of pathology, 1998-11, Vol.153 (5), p.1501-1510

1998

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Fullerene Resist Materials for the 32 nm Node and Beyond

Advanced functional materials, 2008-07, Vol.18 (13), p.1977-1982

2008

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Incomplete penetrance of GLMN gene c.395-1G>C mutation in a family with glomuvenous malformations

International journal of dermatology, 2014-11, Vol.53 (11), p.1362-1364

2014

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Genetic counselling and high-penetrance susceptibility gene analysis reveal the novel CDKN2A p.D84V (c.251A>T) mutation in melanoma-prone families from Italy

Melanoma research, 2017-04, Vol.27 (2), p.97-103

2017

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Glomuvenous malformations with smooth muscle and eccrine glands: unusual histopathologic features in a familial setting

Journal of cutaneous pathology, 2014-03, Vol.41 (3), p.308-315

2014

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A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations

Experimental dermatology, 2011-12, Vol.20 (12), p.1032-1034

2011

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Fullerene Resist Materials for the 32nm Node and Beyond

Advanced functional materials, 2008-07, Vol.18 (13), p.1977-1982

2008

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Interaction of the Anthracycline 4'-Iodo-4'-Deoxydoxorubicin with Amyloid Fibrils: Inhibition of Amyloidogenesis

Proceedings of the National Academy of Sciences - PNAS, 1995-03, Vol.92 (7), p.2959-2963

1995

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A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations: Letter to the Editor

Experimental dermatology, 2011-12, Vol.20 (12), p.1032-1034

2011

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Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarction

British Heart Journal, 1995-12, Vol.74 (6), p.584-591

1995

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Chemically amplified molecular resists for e-beam lithography

Microelectronic engineering, 2008-05, Vol.85 (5-6), p.764-767

2008

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pH-Dependent gold nanoparticle self-organization on functionalized Si/SiO2 surfaces

Journal of experimental nanoscience, 2006-09, Vol.1 (3), p.333-353

2006

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Coexistence of mitochondrial DNA and β myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure

Heart (British Cardiac Society), 1998-12, Vol.80 (6), p.548-558

1998

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Gene symbol: SCN5A. Disease: Brugada syndrome

Human genetics, 2005-12, Vol.118 (3-4), p.536-536

2005

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Survey on antimicrobial prescribing patterns in small animal veterinary practice in Emilia Romagna, Italy

RAPID EMERGENCE OF CANDIDA AURIS IN NORTH ITALY, 2019 TO JULY 2022

Depletion study of PCDD/Fs and dioxin-like PCBs concentrations in contaminated home-produced eggs: Preliminary study

Management of vaccine-related issues during a pandemic emergency: activation of a referral center

Decrease in Hospital Admissions for Transient Ischemic Attack, Mild, and Moderate Stroke During the COVID-19 Era

Giant Retroperitoneal Myelolipoma: An Unusual Diagnostic GI Challenge—Case Report and Review of the Literature

A novel AβPP mutation exclusively associated with cerebral amyloid angiopathy

Proceedings of the 29th ISFG Congress

Analysis of Vλ-Jλ expression in plasma cells from primary (AL) amyloidosis and normal bone marrow identifies 3r(λIII) as a new amyloid-associated germline gene segment

When Should Cardiologists Suspect Anderson-Fabry Disease?

Cost-effectiveness of mechanical thrombectomy for acute ischemic stroke in Brazil: Results from the RESILIENT trial

Mitochondrial DNA Mutations and Mitochondrial Abnormalities in Dilated Cardiomyopathy

Fullerene Resist Materials for the 32 nm Node and Beyond

Incomplete penetrance of GLMN gene c.395-1G>C mutation in a family with glomuvenous malformations

Genetic counselling and high-penetrance susceptibility gene analysis reveal the novel CDKN2A p.D84V (c.251A>T) mutation in melanoma-prone families from Italy

Glomuvenous malformations with smooth muscle and eccrine glands: unusual histopathologic features in a familial setting

A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations

Fullerene Resist Materials for the 32nm Node and Beyond

Interaction of the Anthracycline 4'-Iodo-4'-Deoxydoxorubicin with Amyloid Fibrils: Inhibition of Amyloidogenesis

A novel mutation of the glomulin gene in an Italian family with autosomal dominant cutaneous glomuvenous malformations: Letter to the Editor

Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarction

Chemically amplified molecular resists for e-beam lithography

pH-Dependent gold nanoparticle self-organization on functionalized Si/SiO2 surfaces

Coexistence of mitochondrial DNA and β myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure

Gene symbol: SCN5A. Disease: Brugada syndrome

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