MIOZZO, MONICA ROSA
MIOZZO, MONICA ROSA
Dipartimento di Scienze della Salute
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome
2020 L. Fontana, M.F. Bedeschi, G.A. Cagnoli, J. Costanza, N. Persico, S. Gangi, M. Porro, P. Ajmone, P. Colapietro, C. Santaniello, M. Crippa, S.M. Sirchia, M. Miozzo, S. Tabano
19p deletion in recurring leiomyosarcoma lesions from the same patient
2000 P. Riva, L. Dalprá, V. Gualandri, M. Volontè, M. Miozzo, R. Malgara, A. F. Conti, L. Larizza
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins
2018 L. Paganini, L.A. Hadi, M. Chetta, D. Rovina, L. Fontana, P. Colapietro, E. Bonaparte, L. Pezzani, P. Marchisio, S.M. Tabano, J. Costanza, S.M. Sirchia, L. Riboni, D. Milani, M. Miozzo
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls
2019 S. Tabano, A. Caldiroli, A. Terrasi, P. Colapietro, S. Grassi, G.S. Carnevali, L. Fontana, M. Serati, V. Vaira, A.C. Altamura, M. Miozzo, M. Buoli
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes
2016 S. Russo, L. Calzari, A. Mussa, E. Mainini, M. Cassina, S. Di Candia, M. Clementi, S. Guzzetti, S. Tabano, M. Miozzo, S. Sirchia, P. Finelli, P. Prontera, S. Maitz, G. Sorge, A. Calcagno, M. Maghnie, M.T. Divizia, D. Melis, E. Manfredini, G.B. Ferrero, V. Pecile, L. Larizza
A novel de novo DDX3X missense variant in a female with brachycephaly and intellectual disability : a case report
2021 G. Moresco, J. Costanza, C. Santaniello, O. Rondinone, F. Grilli, E. Prada, S. Orcesi, I. Coro, A. Pichiecchio, P. Marchisio, M. Miozzo, L. Fontana, D. Milani
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome
2018 L. Paganini, C. Pesenti, D. Milani, L. Fontana, S. Motta, S.M. Sirchia, G. Scuvera, P. Marchisio, S. Esposito, C.M. Cinnante, S.M. Tabano, M.R. Miozzo
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency
2001 R. Pallotta, L. Dalprà, M. Miozzo, T. Ehresmann, P. Fusilli
A synovial sarcoma with t(x;18)(p11;q11) in a patient with turner's syndrome
1992 M. Miozzo, G. Sozzi, C.T. Cariani, M.A. Pierotti, G.D. Porta, S.D. Palma, R. Luksch, A. Azzarelli
A t( 10; 17) translocation creates the RET/PTC2 chimeric transforming sequence in papillary thyroid carcinoma
1994 G. Sozzi, L. Bongarzone, M. Miozzo, M.G. Borrello, M.G. Butti, G.D. Porta, M.A. Pierotti, S. Pilotti
A t(2;3)(q12-13;p24-25) in follicular thyroid adenomas
1992 G. Sozzi, M. Miozzo, T.C. Cariani, I. Bongarzone, S. Pilotti, M.A. Pierotti, G. Della Porta
A Targeted Next-Generation Sequencing Panel to Genotype Gliomas
2022 M. Guarnaccia, L. Guarnaccia, V. La Cognata, S.E. Navone, R. Campanella, A. Ampollini, M. Locatelli, M. Miozzo, G. Marfia, S. Cavallaro
A tumor suppressor locus in familial and sporadic chordoma maps to 1p36
2000 M. Miozzo, L. Dalprà, P. Riva, M. Volontè, F. Macciardi, S. Pericotti, M. G. Tibiletti, M. Cerati, K. Rohde, L. Larizza, A. M. Fuhrman Conti
Advanced forecasting of SARS-CoV-2-related deaths in Italy, Germany, Spain, and New York State
2020 G. Sotgiu, A.G. Gerli, S. Centanni, M. Miozzo, G.W. Canonica, J.B. Soriano, J.C. Virchow
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas
2008 S. Tabano, C. Mandò, P. Colapietro, S. Zanutto, S. Calabrese, P. Pileri, V. Signorelli, M.R. Miozzo, I. Cetin
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva
2005 B. Gentilin, F.R. Grati, P. Invernizzi, C. Selmi, P. Busatto, S.M. Sirchia, F. Rossella, G. Simoni, M. Miozzo
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer
2020 S. Tabano, J. Azzollini, C. Pesenti, S. Lovati, J. Costanza, L. Fontana, B. Peissel, M. Miozzo, S. Manoukian
Angiogenesis in human brain tumors : screening of drug response through a patient-specific cell platform for personalized therapy
2018 L. Guarnaccia, S. Navone, E. Trombetta, C. Cordiglieri, A. Cherubini, F. Crisà, P. Rampini, M. Miozzo, L. Fontana, M. Caroli, M. Locatelli, L. Riboni, R. Campanella, G. Marfia
Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension
2009 C. Mandò, P. Antonazzo, S. Tabano, S. Zanutto, P. Pileri, E. Somigliana, F. Colleoni, A. Martinelli, A. Zolin, C. Benedetto, L. Marozio, I. Neri, F. Facchinetti, M. Miozzo, I. Cetin
Angiotensin-converting enzyme and alpha-adducin polymorphisms in preeclamptic mothers and fetuses
2008 C. Mando, P. Antonazzo, S. Tabano, F. Colleoni, A. Martinelli, S. Calabrese, C. Benedetto, L. Marozio, F. Facchinetti, M. Miozzo, I. Cetin