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Gynecologic and Obstetric Investigation|July 18, 2003
Association between plasminogen activator inhibitor 1 gene polymorphisms and preeclampsiaDora Fabbro, Angela V D'Elia, Riccardo Spizzo, et al.
Legal Medicine (Tokyo, Japan)|March 28, 2024
Filamin C (FLNC) truncating mutation in a fatal arrhythmogenic left ventricular cardiomyopathy (ALVC)Francesco Simonit, Ugo Da Broi, Angela Valentina D'Elia, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|April 18, 2007
Investigation of endothelin-1 type A receptor gene polymorphism (-231 G > A) in preeclampsia susceptibilityVeronica Lisi, Delia M Paternoster, Anna Stecca, et al.
Cancer|April 28, 2011
Concomitant ABCG2 overexpression and FLT3-ITD mutation identify a subset of acute myeloid leukemia patients at high risk of relapseMario Tiribelli, Antonella Geromin, Angela Michelutti, et al.
American Journal of Hematology|June 14, 2013
BAALC overexpression retains its negative prognostic role across all cytogenetic risk groups in acute myeloid leukemia patientsDaniela Damiani, Mario Tiribelli, Alessandra Franzoni, et al.
Hematological Oncology|July 14, 2009
Two novel NPM1 mutations in a therapy-responder AML patientAnnalisa Pianta, Dora Fabbro, Daniela Damiani, et al.
American Journal of Clinical Pathology|June 21, 2007
Markers of the uPA system and common prognostic factors in breast cancerAlessandro Marco Minisini, Dora Fabbro, Carla Di Loreto, et al.
Leukemia Research|February 4, 2010
Fludarabine-based induction therapy does not overcome the negative effect of ABCG2 (BCRP) over-expression in adult acute myeloid leukemia patientsDaniela Damiani, Mario Tiribelli, Angela Michelutti, et al.
Gynecologic and Obstetric Investigation|April 19, 2002
Frequency of factor V, prothrombin and methylenetetrahydrofolate reductase gene variants in preeclampsiaAngela V D'Elia, Lorenza Driul, Roberta Giacomello, et al.
Molecular Vision|August 8, 2007
A deletion 3' to the PAX6 gene in familial aniridia casesAngela Valentina D'Elia, Lucia Pellizzari, Dora Fabbro, et al.
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