MASSA, VALENTINA
MASSA, VALENTINA
Dipartimento di Scienze della Salute
Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies
2024 E. Di Fede, A. Lettieri, E. Taci, S. Castiglioni, S. Rebellato, C. Parodi, E.A. Colombo, P. Grazioli, F. Natacci, P. Marchisio, L. Pezzani, G. Fazio, D. Milani, V. Massa, C. Gervasini
SMC1A epilepsy syndrome: clinical data from a large international cohort
2024 E. Gibellato, P. Cianci, M. Mariani, B. Parma, S. Huisman, R. Śmigiel, A. Bisgaard, V. Massa, C. Gervasini, A. Moretti, A. Cattoni, A. Biondi, A. Selicorni
Long-Term Effects of SARS-CoV-2 Infection in Hospitalized Children: Findings from an Italian Single-Center Study
2024 V. Calcaterra, V.M. Tagi, E. D'Auria, A. Lai, S. Zanelli, C. Montanari, E. Maria Biganzoli, G. Marano, E. Borghi, V. Massa, A. Riva, G. Zuccotti
Editorial: Maternal-foetal crosstalk impacts on offspring development
2023 P. Ybot-Gonzalez, N.D.E. Greene, A.J. Copp, D.J. Henderson, V. Massa
Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency
2023 R. Oleari, A. Lettieri, S. Manzini, A. Paganoni, V. André, P. Grazioli, M. Busnelli, P. Duminuco, A. Vitobello, C. Philippe, V. Bizaoui, H.L. Storr, F. Amoruso, F. Memi, V. Vezzoli, V. Massa, P. Scheiffele, S.R. Howard, A. Cariboni
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner ear
2023 C. Chiereghin, M. Robusto, M.A. Lewis, S. Caetano, V. Massa, P. Castorina, U. Ambrosetti, K.P. Steel, S. Duga, R. Asselta, G. Soldà
LAM cells as potential drivers of senescence in lymphangioleiomyomatosis microenvironment
2022 C. Bernardelli, S. Ancona, M. Lazzari, A. Lettieri, P. Selvaggio, V. Massa, C.C.G. Gervasini, F. DI MARCO, R. Chiaramonte, E.A. Lesma
Long-term analysis of the effects of COVID-19 in people with epilepsy: Results from a multicenter on-line survey across the pandemic waves
2022 C. Parodi, I. Viganò, E. Ottaviano, V. Massa, E. Borghi, S. Beretta, J.C. Di Francesco, V. Badioni, A. Vignoli
Potential role of STAG1 mutations in genetic predisposition to childhood hematological malignancies
2022 C. Saitta, S. Rebellato, L.R. Bettini, G. Giudici, N. Panini, E. Erba, V. Massa, F. Auer, U. Friedrich, J. Hauer, A. Biondi, G. Fazio, G. Cazzaniga
Feasibility and acceptability of saliva-based testing for the screening of SARS-CoV-2 infection in prison
2022 C. Parodi, E. Ottaviano, N. Cocco, S. Ancona, S. Bianchi, V. Massa, R. Bartolotti, B. Pezzoni, R. Giuliani, E. Borghi, R. Ranieri
KMT2A : umbrella gene for multiple diseases
2022 S. Castiglioni, E. Di Fede, C. Bernardelli, A. Lettieri, C. Parodi, P. Grazioli, E.A. Colombo, S. Ancona, D. Milani, E. Ottaviano, E. Borghi, V. Massa, F. Ghelma, A. Vignoli, E. Lesma, C. Gervasini
Epigenetic disorders: Lessons from the animals-animal models in chromatinopathies
2022 E. Di Fede, P. Grazioli, A. Lettieri, C. Parodi, S. Castiglioni, E. Taci, E.A. Colombo, S. Ancona, A. Priori, C. Gervasini, V. Massa
Identical EP300 variant leading to Rubinstein–Taybi syndrome with different clinical and immunologic phenotype
2022 F. Saettini, G. Fazio, M.T. Bonati, D. Moratto, V. Massa, E. Di Fede, S. Castiglioni, D. Marchetti, M. Chiarini, A. Sottini, M. Iascone, G. Cazzaniga, L. Imberti, A. Biondi, C. Gervasini, R. Badolato
Maternal risk factors associated with antepartum stillbirth
2022 S. Raimondi, V. Massa, C. Ravaldi, A. Vannacci, G. Bulfamante, A. Marconi, L. Avagliano
Role of Cytoskeletal Diaphanous-Related Formins in Hearing Loss
2022 C. Chiereghin, M. Robusto, V. Massa, P. Castorina, U. Ambrosetti, R. Asselta, G. Soldà
The differential roles for neurodevelopmental and neuroendocrine genes in shaping gnrh neuron physiology and deficiency
2021 R. Oleari, V. Massa, A. Cariboni, A. Lettieri
Insights into the role of the microbiota and of short-chain fatty acids in Rubinstein–Taybi syndrome
2021 E. Di Fede, E. Ottaviano, P. Grazioli, C. Ceccarani, A. Galeone, C. Parodi, E.A. Colombo, G. Bassanini, G. Fazio, M. Severgnini, D. Milani, E. Verduci, T. Vaccari, V. Massa, E. Borghi, C. Gervasini
Chromatin Imbalance as the Vertex Between Fetal Valproate Syndrome and Chromatinopathies
2021 C. Parodi, E. Di Fede, A. Peron, I. Viganò, P. Grazioli, S. Castiglioni, R.H. Finnell, C. Gervasini, A. Vignoli, V. Massa
Semaphorin Regulation by the Chromatin Remodeler CHD7 : An Emerging Genetic Interaction Shaping Neural Cells and Neural Crest in Development and Cancer
2021 A. Lettieri, R. Oleari, A.J.J. Paganoni, C. Gervasini, V. Massa, A. Fantin, A. Cariboni
Editorial: Impact on Embryonic Development of Chromatin Remodeling Alterations
2021 C. Gervasini, M. Garcia-Dominguez, V. Massa