MARIANI, MILENA

MARIANI, MILENA  

Universita' degli Studi di MILANO  

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Risultati 1 - 9 di 9 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Lithium ameliorates neural differentiation restoring cell death balance in Cornelia de Lange syndrome 2D and 3D models 2026 Parodi, ChiaraLettieri, AntonellaGrazioli, PaoloDi Fede, ElisabettaGrassi, SaraTaci, EsiToscani, AndreaPrioni, SimonaColombo, Elisa AdeleRasetti, SilviaMariani, MilenaCorti, StefaniaFinelli, PalmaPrinetti, AlessandroConti, LucianoGervasini, CristinaMassa, Valentina + Article (author) -
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer Predisposition 2025 Rigotti, LauraLettieri, AntonellaCastiglioni, SilviaMariani, MilenaTotaro, SimonaGervasini, CristinaMassa, Valentina + Article (author) -
SMC1A epilepsy syndrome: clinical data from a large international cohort 2024 Gibellato, ElisabettaMariani, MilenaMassa, ValentinaGervasini, Cristina + Article (author) -
Chromatinopathies: a focus on Cornelia de Lange Syndrome 2020 Avagliano, LauraParenti, IlariaGrazioli, PaoloDi Fede, ElisabettaParodi, ChiaraMariani, MilenaGervasini, CristinaMassa, Valentina + Article (author) -
Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohort 2018 Mariani, MilenaGervasini, Cristina C. + Article (author) -
13q mosaic deletion including RB1 associated to mild phenotype and no cancer outcome-case report and review of the literature 2018 Bestetti I.Sironi A.Catusi I.Mariani M.Larizza L.Castronovo C.Finelli P. + Article (author) -
Integrating molecular and structural findings: Wnt as a possible actor in shaping cognitive impairment in Cornelia de Lange syndrome 2017 L. AvaglianoP. GrazioliMARIANI, MILENAG.P. BulfamanteV. Massa + Article (author) -
Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange-overlapping phenotype 2016 I. ParentiC. GervasiniJ. AzzolliniA. CeredaM. MarianiL. Larizza + Article (author) -
Cervical spine malformation in Cornelia de Lange syndrome: a report of three patients 2014 M. MarianiA. CeredaC. Gervasini + Article (author) -