MARIANI, MILENA

MARIANI, MILENA  

Universita' degli Studi di MILANO  

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Titolo Data di pubblicazione Autori Tipo File Abstract
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) -