I. Foffa

发表

Adenosine A2A receptor gene polymorphism (1976C>T) affects coronary flow reserve response during vasodilator stress testing in patients with non ischemic-dilated cardiomyopathy

E. Picano, A. Borghini, R. Sicari, 2011, Pharmacogenetics and genomics.

Small-caliber vascular grafts based on a piezoelectric nanocomposite elastomer: Mechanical properties and biocompatibility.

Alice Rita Salgarella, L. Vannozzi, L. Ricotti, 2019, Journal of the mechanical behavior of biomedical materials.

Fabrication and in-vitro characterization of a polymeric aortic valve for minimally invasive valve replacement.

S. Celi, E. Gasparotti, E. Vignali, 2020, Journal of the mechanical behavior of biomedical materials.

Maternal and paternal environmental risk factors, metabolizing GSTM1 and GSTT1 polymorphisms, and congenital heart disease.

E. Picano, L. Ait-Ali, M. Andreassi, 2011, The American journal of cardiology.

Smoking and congenital heart disease: the epidemiological and biological link.

L. Ait-Ali, M. Andreassi, E. Gianicolo, 2010, Current pharmaceutical design.

[Genetic screening of Gata4 and Nkx2.5 mutations in hereditary congenital heart defects: 5 familial cases].

L. Ait-Ali, M. Andreassi, I. Foffa, 2011, Recenti progressi in medicina.

Angiotensin-converting enzyme insertion/deletion polymorphism is a risk factor for thoracic aortic aneurysm in patients with bicuspid or tricuspid aortic valves.

M. Andreassi, A. Mazzone, M. Mariani, 2012, The Journal of thoracic and cardiovascular surgery.

Hypothesis-free secretome analysis of thoracic aortic aneurysm reinforces the central role of TGF-β cascade in patients with bicuspid aortic valve.

S. Rocchiccioli, N. Ucciferri, M. Andreassi, 2017, Journal of cardiology.

Novel TGFBR2 and known missense SMAD3 mutations: two case reports of thoracic aortic aneurysms.

M. Andreassi, S. Sabina, I. Foffa, 2015, The Annals of thoracic surgery.

Novel TGFBR 2 and Known Missense SMAD 3 Mutations : Two Case Reports of Thoracic Aortic Aneurysms

M. Andreassi, S. Sabina, I. Foffa, 2014 .

Maternal Environmental Exposure, Infant GSTP1 Polymorphism, and Risk of Isolated Congenital Heart Disease

L. Ait-Ali, M. Andreassi, E. Gianicolo, 2013, Pediatric Cardiology.

Targeted Next-Generation Sequencing in Patients with Non-syndromic Congenital Heart Disease

L. Ait-Ali, A. Borghini, M. Andreassi, 2018, Pediatric Cardiology.

Ascending aortic aneurysm in a patient with bicuspid aortic valve, positive history of systemic autoimmune diseases and common genetic factors: a case report

L. Ait-Ali, M. Andreassi, A. Mazzone, 2009, Cardiovascular ultrasound.

A Functional Aryl Hydrocarbon Receptor Genetic Variant, Alone and in Combination with Parental Exposure, is a Risk Factor for Congenital Heart Disease

L. Ait-Ali, A. Borghini, M. Andreassi, 2018, Cardiovascular Toxicology.

Lack of Association of the 3′-UTR Polymorphism (rs1017) in the ISL1 Gene and Risk of Congenital Heart Disease in the White Population

L. Ait-Ali, M. Andreassi, C. Vecoli, 2013, Pediatric Cardiology.

Congenital Heart Disease: The Crossroads of Genetics, Epigenetics and Environment

M. Andreassi, C. Vecoli, I. Foffa, 2014, Current Genomics.

Bilayered Fibrin-Based Electrospun-Sprayed Scaffold Loaded with Platelet Lysate Enhances Wound Healing in a Diabetic Mouse Model

P. Losi, G. Soldani, I. Foffa, 2020, Nanomaterials.

Carboxymethyl Cellulose-Based Hydrogel Film Combined with Umbilical Cord Blood Platelet gel as an Innovative Tool for Chronic Wound Management: A Pilot Clinical Study.

F. Faita, M. Romanelli, A. Janowska, 2022, The international journal of lower extremity wounds.

Plasminogen-Loaded Fibrin Scaffold as Drug Delivery System for Wound Healing Applications

P. Losi, G. Soldani, I. Foffa, 2022, Pharmaceutics.

Next generation sequencing in cardiovascular diseases.

M. Andreassi, C. Vecoli, I. Foffa, 2012, World journal of cardiology.

Leukocyte telomere shortening in grown-up patients with congenital heart disease.

E. Picano, L. Ait-Ali, A. Borghini, 2016, International journal of cardiology.

Genetic polymorphisms in XRCC1, OGG1, APE1 and XRCC3 DNA repair genes, ionizing radiation exposure and chromosomal DNA damage in interventional cardiologists.

E. Picano, M. Andreassi, I. Foffa, 2009, Mutation research.

Functional characterization and circulating expression profile of dysregulated microRNAs in BAV-associated aortopathy

L. Ait-Ali, A. Borghini, M. Andreassi, 2019, Heart and Vessels.

Genetic score based on high-risk genetic polymorphisms and early onset of ischemic heart disease in an Italian cohort of ischemic patients.

A. L'Abbate, T. Sampietro, C. Carpeggiani, 2014, Thrombosis research.

Circulating soluble receptor for advanced glycation end-product levels are decreased in patients with calcific aortic valve stenosis.

A. Vianello, S. Del Turco, G. Basta, 2010, Atherosclerosis.

Cumulative patient effective dose and acute radiation-induced chromosomal DNA damage in children with congenital heart disease

Eugenio Picano, Eliseo Vano, Maria Grazia Andreassi, 2009, Heart.

Germline hereditary, somatic mutations and microRNAs targeting-SNPs in congenital heart defects.

L. Ait-Ali, M. Andreassi, S. Sabina, 2013, Journal of molecular and cellular cardiology.

Sequencing of NOTCH1, GATA5, TGFBR1 and TGFBR2 genes in familial cases of bicuspid aortic valve

M. Andreassi, M. Mariani, P. Festa, 2013, BMC Medical Genetics.

N-acetyl cysteine reduces chromosomal DNA damage in circulating lymphocytes during cardiac catheterization procedures: a pilot study.

E. Picano, M. Andreassi, I. Foffa, 2012, International journal of cardiology.

Health Risk and Biological Effects of Cardiac Ionising Imaging: From Epidemiology to Genes

M. Andreassi, I. Foffa, Monica Cresci, 2009, International journal of environmental research and public health.

The Positive Impact of Early Frailty Levels on Mortality in Elderly Patients with Severe Aortic Stenosis Undergoing Transcatheter/Surgical Aortic Valve Replacement

S. Del Turco, G. Basta, A. Mazzone, 2023, Journal of cardiovascular development and disease.

miRNome Profiling in Bicuspid Aortic Valve-Associated Aortopathy by Next-Generation Sequencing

L. Ait-Ali, A. Borghini, M. Andreassi, 2017, International journal of molecular sciences.

[Bicuspid aortic valve: epidemiology, genetics and clinics].

L. Ait-Ali, P. Festa, I. Foffa, 2012, Recenti progressi in medicina.

A Copper nanoparticles-based polymeric spray coating: Nanoshield against Sars-Cov-2

M. Pistello, M. D’Acunto, P. Losi, 2022, Journal of Applied Biomaterials & Functional Materials.

A Functional Aryl Hydrocarbon Receptor Genetic Variant, Alone and in Combination with Parental Exposure, is a Risk Factor for Congenital Heart Disease

L. Ait-Ali, A. Borghini, M. Andreassi, 2018, Cardiovascular Toxicology.

Diagnostic and therapeutic radiation exposure in children: new evidence and perspectives from a biomarker approach

L. Ait-Ali, M. Andreassi, I. Foffa, 2006, Pediatric Radiology.

Marine Collagen-Based Bioink for 3D Bioprinting of a Bilayered Skin Model

P. Losi, G. Soldani, A. Mezzetta, 2023, Pharmaceutics.

3'UTR SNPs and Haplotypes in the GATA4 Gene Contribute to the Genetic Risk of Congenital Heart Disease.

L. Ait-Ali, M. Andreassi, S. Sabina, 2016, Revista espanola de cardiologia.

Ascending aortic aneurysm in a patient with bicuspid aortic valve, positive history of systemic autoimmune diseases and common genetic factors: a case report

L. Ait-Ali, M. Andreassi, A. Mazzone, 2009, Cardiovascular ultrasound.

Preliminary Outcomes of Zone 2 Thoracic Endovascular Aortic Repair Using Castor Single-Branched Stent Grafts: A Single-Center Experience

C. Palmieri, M. Murzi, I. Foffa, 2023, Journal of clinical medicine.

Whole Exome Sequencing Uncovers the Genetic Complexity of Bicuspid Aortic Valve in Families with Early Onset Complications

D. Milewicz, M. Bissell, M. Andreassi, 2024, medRxiv.