SIRCHIA, SILVIA MARIA

SIRCHIA, SILVIA MARIA  

Dipartimento di Scienze della Salute  

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Risultati 1 - 20 di 104 (tempo di esecuzione: 0.0 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 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 perspective on diet, epigenetics and complex diseases: where is the field headed next? 2022 Silvana PileggiSilvia Maria Sirchia + Article (author) -
A perspective on diet, epigenetics and complex diseases: where is the field headed next? 2022 Pileggi, SilvanaSirchia, Silvia Maria + Article (author) -
Absence of detectable maternal DNA and identification of proviral HIV in the cord blood of two infants who became HIV-infected 1997 G. SimoniSACCHI, LAURAS.M. SirchiaI.M. GaragiolaT. PersicoG. PardiA.E. Semprini + Article (author) -
An epigenetic event may underlies the TSC features in TSC2 ASM cells 2009 E. LesmaS. AnconaS.M. SirchiaV. GrandeE. ChiaramonteS. BosariA.M. Di GiulioA. Gorio Conference Object -
Analisi del metiloma negli ultralongevi e nei loro figli e stato di salute 2011 D. MariS.M. SirchiaS. TabanoG. Vitale + Article (author) -
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 2005 B. GentilinF.R. GratiP. InvernizziC. SelmiS.M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Aneuploid correction and confined placental mosaicism 1996 G. SimoniS.M. Sirchia + Article (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) -
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 2004 F.R. GratiS.M. SirchiaB. GentilinF. RossellaL. RamoscelliG. BulfamanteI. CetinG. SimoniM. Miozzo + Article (author) -
Blood fetal microchimerism in primary biliary cirrhosis 2000 S.M. SirchiaP.M. BattezzatiM. ZuinF. RossellaF. PeregoM. BignottoM. Podda + Article (author) -
Characterization of four microsatellites in an Italian population and their application to paternity testing 1996 S.M. SirchiaI. Garagiola + Article (author) -
Characterization of human TSC2 cells derived from a TSC/LAM patient chylous effusion 2011 E. LesmaS. AnconaS.M. SirchiaE. OrpianesiA.M. Di GiulioA. Gorio + Conference Object -
Characterization of LAM/TSC cells isolated from patient chylous 2010 E. LesmaS. AnconaV. GrandeS.M. SirchiaE. ChiaramonteS. BosariA.M. Di GiulioA. Gorio Conference Object -
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) -