关注
Cristina Mazzaccara
Cristina Mazzaccara
Ricercatore universitario, Dipartimento di Medicina Molecolare e Biotecnologie Mediche
在 unina.it 的电子邮件经过验证
标题
引用次数
引用次数
年份
Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss
G Fortunato, E Marciano, F Zarrilli, C Mazzaccara, M Intrieri, G Calcagno, ...
Clinical chemistry 50 (11), 2012-2018, 2004
1542004
Age-related reference intervals of the main biochemical and hematological parameters in C57BL/6J, 129SV/EV and C3H/HeJ mouse strains
C Mazzaccara, G Labruna, G Cito, M Scarfò, M De Felice, L Pastore, ...
PloS one 3 (11), e3772, 2008
1472008
A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women
G Fortunato, P Rubba, S Panico, D Trono, N Tinto, C Mazzaccara, ...
Atherosclerosis 167 (1), 141-148, 2003
852003
Contemporary genetic testing in inherited cardiac disease: tools, ethical issues, and clinical applications
F Girolami, G Frisso, M Benelli, L Crotti, M Iascone, R Mango, ...
Journal of Cardiovascular Medicine 19 (1), 1-11, 2018
732018
Exercise, immune system, nutrition, respiratory and cardiovascular diseases during COVID-19: a complex combination
O Scudiero, B Lombardo, M Brancaccio, C Mennitti, A Cesaro, F Fimiani, ...
International Journal of Environmental Research and Public Health 18 (3), 904, 2021
582021
Warfarin anticoagulant therapy: a Southern Italy pharmacogenetics-based dosing model
C Mazzaccara, V Conti, R Liguori, V Simeon, M Toriello, A Severini, ...
PloS one 8 (8), e71505, 2013
572013
The biological role of vitamins in athletes’ muscle, heart and microbiota
M Brancaccio, C Mennitti, A Cesaro, F Fimiani, M Vano, B Gargiulo, ...
International journal of environmental research and public health 19 (3), 1249, 2022
552022
Haplogroup T is an obesity risk factor: mitochondrial DNA haplotyping in a morbid obese population from southern Italy
C Nardelli, G Labruna, R Liguori, C Mazzaccara, M Ferrigno, ...
BioMed research international 2013 (1), 631082, 2013
552013
Decreased paraoxonase-2 expression in human carotids during the progression of atherosclerosis
G Fortunato, MD Di Taranto, UM Bracale, L Del Guercio, F Carbone, ...
Arteriosclerosis, thrombosis, and vascular biology 28 (3), 594-600, 2008
532008
Mitochondrial diabetes in children: seek and you will find it
C Mazzaccara, D Iafusco, R Liguori, M Ferrigno, A Galderisi, D Vitale, ...
PLoS One 7 (4), e34956, 2012
502012
Yield and clinical significance of genetic screening in elite and amateur athletes
G Limongelli, M Nunziato, V D'Argenio, MV Esposito, E Monda, ...
European journal of preventive cardiology 28 (10), 1081-1090, 2021
492021
Laboratory medicine: Health evaluation in elite athletes
B Lombardo, V Izzo, D Terracciano, A Ranieri, C Mazzaccara, F Fimiani, ...
Clinical Chemistry and Laboratory Medicine (CCLM) 57 (10), 1450-1473, 2019
422019
Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single‐Patient Data Meta‐Analysis in More Than 15,000 Individuals
E Danese, S Raimondi, M Montagnana, A Tagetti, T Langaee, P Borgiani, ...
Clinical Pharmacology & Therapeutics 105 (6), 1477-1491, 2019
382019
Dietary thiols: A potential supporting strategy against oxidative stress in heart failure and muscular damage during sports activity
M Brancaccio, C Mennitti, A Cesaro, F Fimiani, E Moscarella, M Caiazza, ...
International Journal of Environmental Research and Public Health 17 (24), 9424, 2020
372020
Unexplained sudden cardiac arrest in children: clinical and genetic characteristics of survivors
E Monda, B Sarubbi, MG Russo, M Caiazza, C Mazzaccara, J Magrelli, ...
European journal of preventive cardiology 28 (10), 1134-1137, 2021
312021
Functional studies and in silico analyses to evaluate non-coding variants in inherited cardiomyopathies
G Frisso, N Detta, P Coppola, C Mazzaccara, MR Pricolo, A D’Onofrio, ...
International Journal of Molecular Sciences 17 (11), 1883, 2016
292016
Genetic analysis resolves differential diagnosis of a familial syndromic dilated cardiomyopathy: A new case of Alström syndrome
B Lombardo, V D'Argenio, E Monda, A Vitale, M Caiazza, L Sacchetti, ...
Molecular Genetics & Genomic Medicine 8 (7), e1260, 2020
272020
A common polymorphism in the SCN5A gene is associated with dilated cardiomyopathy
C Mazzaccara, G Limongelli, M Petretta, R Vastarella, G Pacileo, ...
Journal of Cardiovascular Medicine 19 (7), 344-350, 2018
252018
The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from Southern Italy
R Liguori, C Mazzaccara, F Pasanisi, P Buono, G Oriani, C Finelli, ...
Nutrition, metabolism and cardiovascular diseases 16 (7), 466-470, 2006
252006
Protein thermodynamic destabilization in the assessment of pathogenicity of a variant of uncertain significance in cardiac myosin binding protein C
MR Pricolo, E Herrero-Galán, C Mazzaccara, MA Losi, ...
Journal of cardiovascular translational research 13, 867-877, 2020
242020
系统目前无法执行此操作,请稍后再试。
文章 1–20