CESARETTI, CLAUDIA
CESARETTI, CLAUDIA
Universita' degli Studi di MILANO
CATSHL syndrome, a new family and phenotypic expansion
2024 S. Cannova, C. Meossi, F. Grilli, D. Milani, F. Alberti, C. Cesaretti, P.G. Marchisio, F. Crosti, L. Pezzani
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes
2024 V. Tritto, P. Bettinaglio, E. Mangano, C. Cesaretti, F. Marasca, C. Castronovo, R. Bordoni, C. Battaglia, V. Saletti, V. Ranzani, B. Bodega, M. Eoli, F. Natacci, P. Riva
New insights into the molecular basis of spinal neurofibromatosis type 1
2023 P. Bettinaglio, E. Mangano, V. Tritto, R. Bordoni, R. Paterra, A. Borghi, M. Volontè, C. Battaglia, V. Saletti, C. Cesaretti, F. Natacci, M.A.B. Melone, M. Eoli, P. Riva
A Translational Approach to Spinal Neurofibromatosis: Clinical and Molecular Insights from a Wide Italian Cohort
2023 R. Paterra, P. Bettinaglio, A. Borghi, E. Mangano, V. Tritto, C. Cesaretti, C. Schettino, R. Bordoni, C. Santoro, S. Avignone, M.E.M. Moscatelli, M. Anna Beatrice Melone, V. Saletti, G. Piluso, F. Natacci, P.V. Riva, M. Eoli
Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome
2022 B. Rinaldi, C. Cesaretti, S. Boito, R. Villa, S. Guerneri, I. Borzani, T. Rizzuti, D. Marchetti, G. Conte, C. Cinnante, F. Triulzi, N. Persico, M. Iascone, F. Natacci
Case Report: The Association Between Chromosomal Anomalies and Cluster A Personality Disorders: The Case of Two Siblings With 16p11.2 Deletion and a Review of the Literature
2021 C.M. Esposito, P. Enrico, D. Sciortino, E. Caletti, G.B. Marchetti, C. Cesaretti, L. Oldani, A. Fiorentini, P. Brambilla
NF1 Alterations are Linked to Increased HER2 Expression in Breast Cancer-Letter
2019 D. Gambini, F. Natacci, C. Cesaretti, N. Fusco
Prenatal detection of 5q14.3 duplication including MEF2C and brain phenotype
2016 C. Cesaretti, L. Spaccini, A. Righini, C. Parazzini, G. Conte, F. Crosti, S. Redaelli, G. Bulfamante, L. Avagliano, M. Rustico
Fetal-MRI prenatal diagnosis of severe bilateral lung hypoplasia : alveolar capillary dysplasia case report
2016 S. Zirpoli, A. Munari, M. Rustico, G. Bulfamante, G. Lista, L. Spaccini, C. Cesaretti
Variability of forebrain commissures in callosal agenesis: A prenatal MR imaging study
2016 C. Cesaretti, M. Nanni, T. Ghi, C. Parazzini, G. Conte, E. Contro, G. Grisolia, A. Righini
Expanding the spectrum of human ganglionic eminence region anomalies on fetal magnetic resonance imaging.
2016 A.M. Righini, C. Cesaretti, G. Conte, C. Parazzini, C. Frassoni, G. Bulfamante, L. Avagliano, F. Inverardi, G. Izzo, M. Rustico
Growth differentiation factor 15 expression and regulation during erythroid differentiation in non transfusion dependent thalassemia syndromes
2013 L. Ronzoni, L. Sonzogni, L. Duca, G. Graziadei, C. Cesaretti, A. Marcon, M.D. Cappellini
Clinical features in sickle cell disease
2012 G. Graziadei, A. Marcon, C. Cesaretti, M. Soldarini, I. Gandolfi, P. Ridolfi, M.D. Cappellini
Splenic and liver involvement in Sickle cell disease
2012 G. Graziadei, A. Marcon, I. Gandolfi, M. Soldarini, E. Poggiali, C. Cesaretti, I.M. Baldini, M.D. Cappellini
Does absolute excess of alpha chains compromise the benefit of splenectomy in patients with thalassemia intermedia?
2012 G. Graziadei, C. Refaldi, W. Barcellini, C. Cesaretti, E. Cassinero, K.M. Musallam, M.D. Cappellini
Le sindromi talassemiche
2011 G. Graziadei, C. Cesaretti, M.D. Cappellini
Sickle cell disease and sickle beta-thalassemia : clinical features
2011 G. Graziadei, M. Soldarini, C. Cesaretti, C. Refaldi, M. Salvatori, E. Cassinerio, M.D. Cappellini
Levels of growth differentiation factor-15 are high and correlate with clinical severity in transfusion-independent patients with β thalassemia intermedia
2011 K. M. Musallam, A. T. Taher, L. Duca, C. Cesaretti, R. Halawi, M. D. Cappellini
Relationship between GDF-15 (Growth differentiation factor 15) and iron overload in thalassemia intermedia patients
2010 L. Duca, I. Nava, G. Graziadei, C. Cesaretti, M.D. Cappellini
Genetic variability of TMPRSS6 gene and its association with iron deficiency anemia
2010 P. Delbini, V. Vaja, G. Graziadei, C. Cesaretti, I. Motta, M.D. Cappellini