| A new case of Smith‐Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth D Carli, GB Ferrero, A Fusillo, P Coppo, R La Selva, F Zinali, ... Clinical Genetics 99 (5), 719-723, 2021 | 10 | 2021 |
| Activating protein-1 family of transcription factors in the human placenta complicated by preeclampsia with and without fetal growth restriction D Marzioni, T Todros, S Cardaropoli, A Rolfo, T Lorenzi, P Ciarmela, ... Placenta 31 (10), 919-927, 2010 | 24 | 2010 |
| Adult phenotype of Beckwith-Wiedemann syndrome D Carli, A Gazzin, C Molinatto, F Sirchia, S Cardaropoli, A Mussa, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27 (Suppl. 2), 1496-1497, 2019 | | 2019 |
| Assisted reproduction techniques and prenatal diagnosis of Beckwith–Wiedemann spectrum presenting with omphalocele A Mussa, D Carli, S Cardaropoli, C Molinatto, GB Ferrero Journal of Assisted Reproduction and Genetics 35, 1925-1926, 2018 | 2 | 2018 |
| Bcl2, p53 and clinical outcome in a series of 138 operable breast cancer patients. F Castiglione, I Sarotto, V Fontana, M Destefanis, A Venturino, S Ferro, ... Anticancer research 19 (5C), 4555-4563, 1999 | 41 | 1999 |
| BECKWITH-WIEDEMANN SPECTRUM (BWSP) AND ADRENOCORTICAL TUMORS: AN INSIGHT INTO CLINICAL AND MOLECULAR CHARACTERISTICS A Campello, D Carli, M Luca, S Vallero, E Tirtei, F Maletta, L Bertero, ... PEDIATRIC BLOOD & CANCER 70, 2023 | | 2023 |
| CGH-array analysis in 466 patients with autism spectrum disorder (ASD): from diagnosis to uncovering new neurodevelopmental disease (NDD) genes D Carli, G Borini, C Davico, L Pavinato, E Nobile, A Gazzin, S Massuras, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 510-510, 2024 | | 2024 |
| Characterization of Activator Protein-1 (AP-1) Family Gene Expression in Placental Mesenchymal Stem Cells derived from Normal and Preeclamptic Pregnancies. A Nuzzo, S Cardaropoli, E Piccoli, A Piazzese, T Todros, A Rolfo PLACENTA 32 (9), A5-A5, 2011 | | 2011 |
| Characterization of Decoy Receptors D6 and DUFFY in Preeclamptic Placental Tissues. D Giuffrida, A Rolfo, E Piccoli, S Cardaropoli, A Nuzzo, C Tersigni, ... REPRODUCTIVE SCIENCES 19 (Supplement 3), 321A-321A, 2012 | | 2012 |
| Clinical and molecular characterization of Beckwith-Wiedemann spectrum patients conceived through assisted reproductive technology D Carli, J Spina, S Russo, G Cocchi, D Milani, E Prada, D Melis, L Tarani, ... EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 329-329, 2022 | | 2022 |
| Clinical and molecular characterization of patients affected by Beckwith‐Wiedemann spectrum conceived through assisted reproduction techniques D Carli, M Operti, S Russo, G Cocchi, D Milani, C Leoni, E Prada, D Melis, ... Clinical Genetics 102 (4), 314-323, 2022 | 7 | 2022 |
| Clinical and molecular characterization of patients with Beckwith-Wiedemann spectrum conceived through assisted reproductive technology D Carli, J Spina, S Russo, G Cocchi, D Milani, E Prada, D Melis, L Tarani, ... Molecular Genetics and Metabolism 132, S66-S66, 2021 | | 2021 |
| Complete blood counts (CBC) in healthy and small for gestational age fetuses A Rolfo, S Cardaropoli, A Morra, C Maconi, T Todros Ceska Ginekologie 67, 41-42, 2002 | | 2002 |
| Correlation between chlamydosporulation, germ tube, phospholipase and proteinase production in Candida albicans. S Cardaropoli, D Fraia, E Menegatti, S Aoki, V Vidotto | 6 | 1997 |
| CORRELATION BETWEEN PHOSPHOLIPASE PRODUCTION IN CRYPTOCOCCUS NEOFORMANS AND ITS VIRULENCE. D DI FRAIA, S Cardaropoli, A Sinicco, S Aoki, G Criseo, V Vidotto | | 1997 |
| Cover Image, Volume 179A, Number 9, September 2019 A Gazzin, D Carli, F Sirchia, C Molinatto, S Cardaropoli, G Palumbo, ... American Journal of Medical Genetics Part A 179 (9), i-i, 2019 | | 2019 |
| De novo missense variants in PHLPP1 cause a specific neurodevelopmental disorder (NDD) with epilepsy C Giovenino, S Trajkova, V Pullano, S Cardaropoli, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 492-492, 2024 | | 2024 |
| Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant A Gazzin, F Fornari, M Niceta, C Leoni, ML Dentici, D Carli, AM Villar, ... European Journal of Human Genetics, 1-8, 2024 | 2 | 2024 |
| Differential expression of Tight Junction proteins in preeclamptic placentae I Benzonelli, S Cardaropoli, A Rolfo, A Nuzzo, D Marzioni, E Piccoli, ... REPRODUCTIVE SCIENCES 17, 328A-328A, 2010 | | 2010 |
| DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity S Trajkova, J Kerkhof, MR Sebastiano, L Pavinato, E Ferrero, C Giovenino, ... Human Genetics and Genomics Advances 5 (3), 2024 | 1 | 2024 |
Francesco FranceschiProfessore Associato Medicina Interna Universita Cattolica在 rm.unicatt.it 的电子邮件经过验证
