au.\*:("CAVALLARI, Ugo")
Results 1 to 13 of 13
Selection :
Lack of association between the P2Y12 receptor gene polymorphism and platelet response to clopidogrel in patients with coronary artery diseaseANGIOLILLO, Dominick J; FERNANDEZ-ORTIZ, Antonio; ESCANED, Javier et al.Thrombosis research. 2005, Vol 116, Num 6, pp 491-497, issn 0049-3848, 7 p.Article
Germline Mosaicism in Achondroplasia Detected in Sperm DNA of the Father of Three Affected SibsNATACCI, Federica; BAFFICO, Maria; CAVALLARI, Ugo et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 6, pp 784-786, issn 1552-4825, 3 p.Article
Influence of the CD14 C260T promoter polymorphism on C-reactive protein levels in patients with coronary artery diseaseBERNARDO, Esther; ANGIOLILLO, Dominick J; BANUELOS, Camino et al.The American journal of cardiology. 2006, Vol 98, Num 9, pp 1182-1184, issn 0002-9149, 3 p.Article
Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristicsZURADELLI, Monica; PEISSEL, Bernard; SANTORO, Armando et al.Breast cancer research and treatment. 2010, Vol 124, Num 1, pp 251-258, issn 0167-6806, 8 p.Article
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnanciesGRATI, Francesca R; SIRCHIA, Silvia M; MIOZZO, Monica et al.European journal of human genetics. 2004, Vol 12, Num 4, pp 272-278, issn 1018-4813, 7 p.Article
De novo balanced chromosome rearrangements in prenatal diagnosisGIARDINO, Daniela; CORTI, Cecilia; COVIELLO, Domenico et al.Prenatal diagnosis. 2009, Vol 29, Num 3, pp 257-265, issn 0197-3851, 9 p.Article
OLR1 gene and coronary artery disease/acute myocardial infarction : replication in an independently collected sample. Authors' replyNOVELLI, Giuseppe; BORGIANI, Paola; GIRELLI, Domenico et al.European journal of human genetics. 2006, Vol 14, Num 8, pp 894-895, issn 1018-4813, 2 p.Article
On the association of the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction or coronary artery diseaseTRABETTI, Elisabetta; BISCUOLA, Michele; CAVALLARI, Ugo et al.European journal of human genetics. 2006, Vol 14, Num 1, pp 127-130, issn 1018-4813, 4 p.Article
Three cases with de novo 6q imbalance and variable prenatal phenotypeGRATI, Francesca R; LALATTA, Faustina; BALDO, Demetrio et al.American journal of medical genetics. 2005, Vol 136A, Num 3, pp 254-258, issn 0148-7299, 5 p.Article
Variability in platelet aggregation following sustained Aspirin and Clopidogrel treatment in patients with coronary heart disease and influence of the 807 C/T polymorphism of the glycoprotein Ia geneANGIOLILLO, Dominick J; FERNANDEZ-ORTIZ, Antonio; ESCANED, Javier et al.The American journal of cardiology. 2005, Vol 96, Num 8, pp 1095-1099, issn 0002-9149, 5 p.Article
Triple X syndrome: characteristics of 42 Italian girls and parental emotional response to prenatal diagnosisLALATTA, Faustina; QUAGLIARINI, Donatella; NARETTO, Valeria Giorgia et al.European journal of pediatrics. 2010, Vol 169, Num 10, pp 1255-1261, issn 0340-6199, 7 p.Article
ALOXSAP gene variants and risk of coronary artery disease : an angiography-based studyGIRELLI, Domenico; MARTINELLI, Nicola; CORROCHER, Roberto et al.European journal of human genetics. 2007, Vol 15, Num 9, pp 959-966, issn 1018-4813, 8 p.Article
Contribution of gene sequence variations of the hepatic cytochrome P450 3A4 enzyme to variability in individual responsiveness to clopidogrelBEITELSHEES, Amber L; MCLEOD, Howard L; MORENO, Raul et al.Arteriosclerosis, thrombosis, and vascular biology. 2006, Vol 26, Num 8, issn 1079-5642, 1681-1683,1895-1900 [9 p.]Article