TABANO, SILVIA MARIA

TABANO, SILVIA MARIA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

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Risultati 1 - 20 di 96 (tempo di esecuzione: 0.005 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
(Epi)genetic profiling of extraembryonic and postnatal tissues from female monozygotic twins discordant for Beckwith–Wiedemann syndrome 2020 Fontana L.Cagnoli G. A.Persico N.Colapietro P.Crippa M.Sirchia s. m.Miozzo M.Tabano S. + Article (author) -
A HS6ST2 gene variant associated with X-linked intellectual disability and severe myopia in two male twins 2018 Paganini, LedaCHETTA, MASSIMILIANORovina, DavideFontana, LauraColapietro, PatriziaBonaparte, EleonoraPezzani, LidiaMarchisio, PaolaTabano, Silvia MSirchia, Silvia MRiboni, LauraMilani, DonatellaMiozzo, Monica + Article (author) -
A miRNome analysis of drug-free manic psychotic bipolar patients versus healthy controls 2019 Tabano S.Caldiroli A.Terrasi A.Colapietro P.Grassi S.Carnevali G. S.Fontana L.Serati M.Vaira V.Altamura A. C.Miozzo M.Buoli M. Article (author) -
A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver–Russell and Beckwith–Wiedemann syndromes 2016 S. TabanoM. MiozzoS. SirchiaP. FinelliL. Larizza + Article (author) -
A novel splice site variant in ITPR1 gene underlying recessive Gillespie syndrome 2018 Paganini, LedaPesenti, ChiaraMilani, DonatellaFontana, LauraMotta, SilviaSirchia, Silvia MariaScuvera, GiuliettaMarchisio, PaolaCinnante, Claudia MariaTabano, Silvia MariaMiozzo, Monica Rosa + Article (author) -
A Rare Case of Urinary Bladder Hamartoma Clinically Mimicking an Urothelial Carcinoma: A Case Report and Review of the Literature 2023 Pescia, CarloPini, GiudittaLopez, GianlucaMalfatto, MatteoBrescia, GloriaTabano, SilviaDel Gobbo, Alessandro Article (author) -
Altered H19 and SNAT2 expression in type 1 IUGR (Intrauterine Growth Restriction) placentas 2008 S. TabanoC. MandòP. ColapietroS. CalabreseP. PileriV. SignorelliM.R. MiozzoI. Cetin + Article (author) -
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 2011 D. MariS.M. SirchiaS. TabanoG. Vitale + Article (author) -
Analysis of BRCA1 and RAD51C promoter methylation in italian families at high-risk of breast and ovarian cancer 2020 Tabano S.Azzollini J.Fontana L.Miozzo M. + Article (author) -
Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension 2009 C. MandòP. AntonazzoS. TabanoP. PileriE. SomiglianaF. ColleoniA. MartinelliA. ZolinM. MiozzoI. Cetin + Article (author) -
Angiotensin-converting enzyme and alpha-adducin polymorphisms in preeclamptic mothers and fetuses 2008 C. MandoS. TabanoM. MiozzoI. Cetin + Book Part (author) -
Assessment of pregnancy dietary intake and association with maternal and neonatal outcomes 2022 De Cosmi V.Tabano S.Fontana L.Privitera G.Alberico D.Colapietro P.Sirchia S.Stampalija T.Tabasso C.Parazzini F.Mosca F.Ferrazzi E.Bosari S.Miozzo M.Agostoni C. + Article (author) -
Assessment of X chromosome Inactivation pattern in BRCA mutation carriers : evidence for an effect of chemotherapy 2008 M. MiozzoS.M. TabanoP. AntonazzoS.M. Sirchia + Article (author) -
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi 2015 L. PaganiniL. FontanaR. SilipigniS. FioriA. CeredaS. SirchiaM. MiozzoS. Tabano + Article (author) -
Beckwith–Wiedemann and IMAGe syndromes : two very different diseases caused by mutations on the same gene 2014 D. MilaniL. PezzaniS. TabanoM. Miozzo Article (author) -
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders 2018 L. FontanaP. D'UrsiS. SirchiaM. MiozzoS. Tabano + Article (author) -
Clinical and molecular diagnosis of beckwith-wiedemann syndrome with single-or multi-locus imprinting disturbance 2021 Fontana L.Tabano S.Maitz S.Colapietro P.Garzia E.Sirchia S. M.Miozzo M. + Article (author) -
Cohesin mutations induce chromatin conformation perturbation of the H19/IGF2 imprinted region and gene expression dysregulation in Cornelia de Lange syndrome cell lines 2021 Silvana PileggiElisa Adele ColomboLaura FontanaPatrizia ColapietroAnnamaria MorottiSilvia TabanoMyriam AlcalayCristina GervasiniMonica MiozzoSilvia Maria Sirchia + Article (author) -
Constitutional ring chromosome 11 mosaicism in a Wilms tumor patient: cytogenetic, molecular and clinico-pathological studies 2010 S. TabanoM. Miozzo + Article (author) -
Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer 2019 Azzollini, JacopoPesenti, ChiaraFontana, LauraPlebani, MaddalenaTabano, SilviaSirchia, Silvia MariaColapietro, PatriziaVERDERIO, PAOLOMiozzo, Monica + Article (author) -