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Maria Luisa Biondi
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15
Ghilardi, Giorgio
12
Guagnellini, Emma
12
Turri, Olivia
11
Scorza, Raffaella
7
Marasini, Bianca
5
Massarotti, Marco
5
Giovannini, Marcello
5
DeMonti, Marco
5
Verduci, Elvira
4
Cozzolino, Mario
4
Riva, Enrica
4
Erario, Maddalena
4
Agostoni, Carlo
4
Brancaccio, Diego
4
Galassi, Andrea
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Geonetwork of Maria Luisa Biondi (preview)
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All Publications
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2009: Verduci Elvira; Scaglioni Silvia; Agostoni Carlo; Radaelli Giovanni; Biondi Marialuisa; Manso Ana S; Riva Enrica; Giovannini Marcello
The relationship of insulin resistance with SNP 276G>T at adiponectin gene and plasma long-chain polyunsaturated fatty acids in obese children.
Pediatric research 2009;66(3):346-9.
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2009: Santus P; Casanova F; Biondi M L; Blasi F; Di Marco F; Centanni S
Stromelysin-1 polymorphism as a new potential risk factor in progression of chronic obstructive pulmonary disease.
Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace / Fondazione clinica del lavoro, IRCCS [and] Istituto di clinica tisiologica e malattie apparato respiratorio, Università di Napoli, Secondo ateneo 2009;71(1):15-20.
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2008: Marasini Bianca; Massarotti Marco; De Monti Marco; Erario Maddalena; Ghilardi Giorgio; Biondi Maria Luisa
Genetic contribution to carotid vascular disease in patients with systemic lupus erythematosus.
Journal of clinical immunology 2008;28(2):131-3.
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2008: Ghilardi Giorgio; Biondi Maria Luisa; Turri Olivia; Pateri Francesca; d'Eril Gianvico Melzi; Scorza Roberto
Genetic control of chemokines in severe human internal carotid artery stenosis.
Cytokine 2008;41(1):24-8.
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2007: Cozzolino Mario; Galassi Andrea; Biondi Maria Luisa; Butti Alessandra; Russo Micol; Longhini Carlo; Gallieni Maurizio; Brancaccio Diego
Decreased serum fetuin-A levels after a single haemodialysis session.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2007;22(1):290-1.
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2007: Cozzolino Mario; Biondi Maria Luisa; Galassi Andrea; Gallieni Maurizio; d'Eril Gian Vico Melzi; Brancaccio Diego
Gene polymorphisms and serum alpha-2-Heremans-Schmid levels in Italian haemodialysis patients.
American journal of nephrology 2007;27(6):639-42.
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2006: Scaglioni Silvia; Verduci Elvira; Salvioni Michela; Biondi Maria Luisa; Radaelli Giovanni; Agostoni Carlo; Giovannini Marcello
PPAR-gamma2 Pro12Ala variant, insulin resistance and plasma long-chain polyunsaturated fatty acids in childhood obesity.
Pediatric research 2006;60(4):485-9.
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2006: Cozzolino Mario; Galassi Andrea; Biondi Maria Luisa; Turri Olivia; Papagni Sergio; Mongelli Nicola; Civita Luigi; Gallieni Maurizio; Brancaccio Diego
Serum fetuin-A levels link inflammation and cardiovascular calcification in hemodialysis patients.
American journal of nephrology 2006;26(5):423-9.
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2006: Ferrari Maria Maddalena; Biondi Maria Luisa; Rossi Gabriela; Grijuela Barbara; Gaita Sara; Perugino Giuseppe; Viganò Paola
Analysis of two polymorphisms in the promoter region of matrix metalloproteinase 1 and 3 genes in women with endometriosis.
Acta obstetricia et gynecologica Scandinavica 2006;85(2):212-7.
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2005: Marasini Bianca; Cossutta Roberta; Selmi Carlo; Pozzi Maria Rosa; Gardinali Marco; Massarotti Marco; Erario Maddalena; Battaglioli Lodovica; Biondi Maria Luisa
Polymorphism of the fractalkine receptor CX3CR1 and systemic sclerosis-associated pulmonary arterial hypertension.
Clinical & developmental immunology 2005;12(4):275-9.
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2005: Gerli GianCarla; Vanelli Chiara; Turri Olivia; Erario Maddalena; Gardellini Angelo; Pugliano Mariateresa; Biondi Maria Luisa
SDF1-3'A gene polymorphism is associated with chronic myeloproliferative disease and thrombotic events.
Clinical chemistry 2005;51(12):2411-4.
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2005: Brancaccio Diego; Biondi Maria Luisa; Gallieni Maurizio; Turri Olivia; Galassi Andrea; Cecchini Federica; Russo Domenico; Andreucci Vittorio; Cozzolino Mario
Matrix GLA protein gene polymorphisms: clinical correlates and cardiovascular mortality in chronic kidney disease patients.
American journal of nephrology 2005;25(6):548-52.
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2005: Ghilardi Giorgio; Biondi Maria Luisa; La Torre Anna; Battaglioli Lodovica; Scorza Roberto
Breast cancer progression and host polymorphisms in the chemokine system: role of the macrophage chemoattractant protein-1 (MCP-1) -2518 G allele.
Clinical chemistry 2005;51(2):452-5.
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2004: Ghilardi Giorgio; Biondi Maria Luisa; Battaglioli Lodovica; Zambon Antonella; Guagnellini Emma; Scorza Roberto
Genetic risk factor characterizes abdominal aortic aneurysm from arterial occlusive disease in human beings: CCR5 Delta 32 deletion.
Journal of vascular surgery : official publication, the Society for Vascular Surgery [and] International Society for Cardiovascular Surgery, North American Chapter 2004;40(5):995-1000.
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2004: Verduci Elvira; Agostoni Carlo; Biondi Maria Luisa; Radaelli Giovanni; Giovannini Marcello; Riva Enrica
Apolipoprotein B gene polymorphism and plasma lipid levels in phenylketonuric children.
Prostaglandins, leukotrienes, and essential fatty acids 2004;71(2):117-20.
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2004: Ghilardi Giorgio; Biondi Maria Luisa; Turri Olivia; Guagnellini Emma; Scorza Roberto
Internal carotid artery occlusive disease and polymorphisms of fractalkine receptor CX3CR1: a genetic risk factor.
Stroke; a journal of cerebral circulation 2004;35(6):1276-9.
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2004: Ghilardi G; Biondi M L; Turri O; Guagnellini E; Scorza R
Ser128Arg gene polymorphism for E-selectin and severity of atherosclerotic arterial disease.
The Journal of cardiovascular surgery 2004;45(2):143-7.
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2003: Ghilardi Giorgio; Biondi Maria Luisa; Erario Maddalena; Guagnellini Emma; Scorza Roberto
Colorectal carcinoma susceptibility and metastases are associated with matrix metalloproteinase-7 promoter polymorphisms.
Clinical chemistry 2003;49(11):1940-2.
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2003: Selmi Carlo; Zuin Massimo; Biondi Maria Luisa; Invernizzi Pietro; Battezzati Pier Maria; Bernini Mara; Meda Francesca; Gershwin M Eric; Podda Mauro
Genetic variants of endothelial nitric oxide synthase in patients with primary biliary cirrhosis: association with disease severity.
Journal of gastroenterology and hepatology 2003;18(10):1150-5.
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2003: Ghilardi Giorgio; Biondi Maria Luisa; Cecchini Federica; DeMonti Marco; Guagnellini Emma; Scorza Roberto
Vascular invasion in human breast cancer is correlated to T-->786C polymorphism of NOS3 gene.
Nitric oxide : biology and chemistry / official journal of the Nitric Oxide Society 2003;9(2):118-22.
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2003: Massarotti Marco; Marasini Bianca; Marchesoni Antonio; Arreghini Marco; Biondi Maria Luisa
Polymorphism in the stromelysin 1 (matrix metalloproteinase 3) promoter gene and severity of rheumatoid arthritis: comment on the article by Constantin et al.
Arthritis and rheumatism 2003;48(9):2695-6.
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2003: Ghilardi Giorgio; Biondi Maria Luisa
Regarding "impaired vasoreactivity despite an increase in plasma nitrite in patients with abdominal aortic aneurysm".
Journal of vascular surgery : official publication, the Society for Vascular Surgery [and] International Society for Cardiovascular Surgery, North American Chapter 2003;37(2):484; author reply 484.
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2003: Ghilardi Giorgio; Biondi Maria Luisa
Regarding "Differential gene expression in human abdominal aorta: aneurysmal versus occlusive disease".
Journal of vascular surgery : official publication, the Society for Vascular Surgery [and] International Society for Cardiovascular Surgery, North American Chapter 2003;37(1):243-4; author reply 244.
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2002: Ghilardi Giorgio; Biondi Maria Luisa; Caputo Maria; Leviti Simona; DeMonti Marco; Guagnellini Emma; Scorza Roberto
A single nucleotide polymorphism in the matrix metalloproteinase-3 promoter enhances breast cancer susceptibility.
Clinical cancer research : an official journal of the American Association for Cancer Research 2002;8(12):3820-3.
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2002: Massarotti Marco; Marchesoni Antonio; Biondi Maria Louisa; Marasini Bianca
Polymorphism in the matrix metalloproteinase-1 promoter gene and severity of rheumatoid arthritis.
The Journal of rheumatology 2002;29(10):2241; author reply 2242.
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2002: Ghilardi Giorgio; Biondi Maria Luisa; DeMonti Marco; Turri Olivia; Guagnellini Emma; Scorza Roberto
Matrix metalloproteinase-1 and matrix metalloproteinase-3 gene promoter polymorphisms are associated with carotid artery stenosis.
Stroke; a journal of cerebral circulation 2002;33(10):2408-12.
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2002: Marasini Bianca; Massarotti Marco; Biondi Maria Luisa
Homocysteine and vascular diseases.
Circulation 2002;106(7):e33.
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2002: Ghilardi Giorgio; Biondi Maria Luisa; DeMonti Marco; Bernini Mara; Turri Olivia; Massaro Federico; Guagnellini Emma; Scorza Roberto
Independent risk factor for moderate to severe internal carotid artery stenosis: T786C mutation of the endothelial nitric oxide synthase gene.
Clinical chemistry 2002;48(7):989-93.
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2002: Invernizzi Pietro; Biondi Maria Luisa; Battezzati Pier Maria; Perego Francesca; Selmi Carlo; Cecchini Federica; Podda Mauro; Simoni Giuseppe
Presence of fetal DNA in maternal plasma decades after pregnancy.
Human genetics 2002;110(6):587-91.
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2002: Verduci E; Riva E; Agostoni C; Leviti S; Fiori L; Lammardo A M; Biondi M L; Giovannini M
Phenylalanine hydroxylase mutations and phenylalanine-tyrosine metabolism in heterozygotes for phenylalanine hydroxylase deficiency.
Acta paediatrica (Oslo, Norway : 1992) 2002;91(7):805-10.
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2001: Ghilardi G; Biondi M L; Mangoni J; Leviti S; DeMonti M; Guagnellini E; Scorza R
Matrix metalloproteinase-1 promoter polymorphism 1G/2G is correlated with colorectal cancer invasiveness.
Clinical cancer research : an official journal of the American Association for Cancer Research 2001;7(8):2344-6.
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2001: Marasini B; Casari S; Zeni S; Turri O; Biondi M L
Stromelysin promoter polymorphism is associated with systemic sclerosis.
Rheumatology (Oxford, England) 2001;40(4):475-6.
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2000: Biondi M L; Turri O; Leviti S; Seminati R; Cecchini F; Bernini M; Ghilardi G; Guagnellini E
MMP1 and MMP3 polymorphisms in promoter regions and cancer.
Clinical chemistry 2000;46(12):2023-4.
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2000: Marasini B; Casari S; Bestetti A; Maioli C; Cugno M; Zeni S; Turri O; Guagnellini E; Biondi M L
Homocysteine concentration in primary and systemic sclerosis associated Raynaud's phenomenon.
The Journal of rheumatology 2000;27(11):2621-3.
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1999: Biondi M L; Turri O; Dilillo D; Stival G; Guagnellini E
Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population.
Clinical chemistry 1999;45(6 Pt 1):897-8.
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1999: Rottoli A; Gianní M L; Verduci E; Biondi M L; Fiori L; Giovannini M; Riva E
Should genetic analysis in newborn screening and a heterozygote test for hyperphenylalaninaemia be recommended? An Italian study.
Journal of medical screening 1999;6(4):193-4.
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