MASSA, VALENTINA
MASSA, VALENTINA
Dipartimento di Scienze della Salute
Extracellular vesicles from II trimester human amniotic fluid as paracrine conveyors counteracting oxidative stress
2024 G. Senesi, L. Guerricchio, M. Ghelardoni, N. Bertola, S. Rebellato, N. Grinovero, M. Bartolucci, A. Costa, A. Raimondi, C. Grange, S. Bolis, V. Massa, D. Paladini, D. Coviello, A. Pandolfi, B. Bussolati, A. Petretto, G. Fazio, S. Ravera, L. Barile, C. Balbi, S. Bollini
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
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
Intrauterine growth in chromatinopathies: A long road for better understanding and for improving clinical management
2024 L. Avagliano, S. Castiglioni, A. Lettieri, C. Parodi, E. Di Fede, E. Taci, P. Grazioli, E.A. Colombo, C. Gervasini, V. Massa
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
Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter
2024 S. Castiglioni, L. Pezzoli, L. Pezzani, A. Lettieri, E. Di Fede, A. Cereda, S. Ancona, A. Gallina, E.A. Colombo, C. Parodi, P. Grazioli, E. Taci, D. Milani, M. Iascone, V. Massa, C. Gervasini
Editorial: Maternal-foetal crosstalk impacts on offspring development
2023 P. Ybot-Gonzalez, N.D.E. Greene, A.J. Copp, D.J. Henderson, V. Massa
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
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
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
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
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
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
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
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
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
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
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
Meconium-stained amniotic fluid and histologic signs of fetal distress in stillbirths
2021 L. Avagliano, V. Massa, G. Bulfamante