CORTI, PAOLA CONSUELO
CORTI, PAOLA CONSUELO
DIPARTIMENTO DI SCIENZE DELLA SALUTE (attivo dal 01/10/2012 al 30/09/2015)
Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato-Oncologia Pediatrica) study group
2024 Corti, P; Ferrari, G; Faraguna, M; Capitoli, G; Longo, F; Corradini, E; Casini, T; Boscarol, G; Pinto, V; Ghilardi, R; Russo, G; Colombatti, R; Mariani, R; Piperno, A
Hb Monza: A novel extensive HBB duplication with preserved α-β subunit interaction and unstable hemoglobin phenotype
2024 Civettini, I; Zappaterra, A; Corti, P; Messina, A; Aroldi, A; Biondi, A; Cavalca, F; Crippa, V; Crosti, F; Ferrari, G; Malighetti, F; Mologni, L; Piperno, A; Ramazzotti, D; Scollo, C; Zambon, A; Rossi, F; Gambacorti-Passerini, C
Reference ranges for complete blood count in children and adolescents with Down syndrome
2024 Lattuada, M; Capitoli, G; Casati, M; Lazzerotti, A; Maglia, O; Ferrari, G; Fossati, C; Biondi, A; Cattoni, A; Corti, P
Pediatric immune myelofibrosis (PedIMF) as a novel and distinct clinical pathological entity
2022 Guerra, F; L'Imperio, V; Bonanomi, S; Spinelli, M; Coliva, T; Dell'Acqua, F; Ferrari, G; Corti, P; Balduzzi, A; Biondi, A; Pagni, F; Saettini, F
Secondary hemophagocytic lymphohystiocytosis in a Rubinstein Taybi syndrome patient
2022 Saettini, F; Radaelli, S; Ocello, L; Ferrari, G; Corti, P; Dell'Acqua, F; Ippolito, D; Foresti, S; Gervasini, C; Badolato, R; Biondi, A
Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond-like syndrome
2020 Saettini, F; Cattoni, A; D'Angiò, M; Corti, P; Maitz, S; Pagni, F; Seminati, D; Pezzoli, L; Iascone, M; Biondi, A; Bonanomi, S
More than an ‘atypical’ phenotype: dual molecular diagnosis of autoimmune lymphoproliferative syndrome and Becker muscular dystrophy
2020 Saettini, F; L'Imperio, V; Fazio, G; Cazzaniga, G; Mazza, C; Moroni, I; Badolato, R; Biondi, A; Corti, P
Rituximab Unveils Hypogammaglobulinemia and Immunodeficiency in Children with Autoimmune Cytopenia
2020 Ottaviano, G; Marinoni, M; Graziani, S; Sibson, K; Barzaghi, F; Bertolini, P; Chini, L; Corti, P; Cancrini, C; D'Alba, I; Gabelli, M; Gallo, V; Giancotta, C; Giordano, P; Lassandro, G; Martire, B; Angarano, R; Mastrodicasa, E; Bava, C; Miano, M; Naviglio, S; Verzegnassi, F; Saracco, P; Trizzino, A; Biondi, A; Pignata, C; Moschese, V
Heterozygous mutation in adenosine deaminase gene in a patient with severe lymphopenia following corticosteroid treatment of autoimmune hemolytic anemia
2018 Tripodi, S; Corti, P; Giliani, S; Lanfranchi, A; Biondi, A; Badolato, R
Mesenchymal stromal cells from Shwachman-Diamond syndrome patients fail to recreate a bone marrow niche in vivo and exhibit impaired angiogenesis
2018 Bardelli, D; Dander, E; Bugarin, C; Cappuzzello, C; Pievani, A; Fazio, G; Pierani, P; Corti, P; Farruggia, P; Dufour, C; Cesaro, S; Cipolli, M; Biondi, A; D'Amico, G
Human aplastic anaemia-derived mesenchymal stromal cells form functional haematopoietic stem cell niche in vivo
2017 Michelozzi, I; Pievani, A; Pagni, F; Antolini, L; Verna, M; Corti, P; Rovelli, A; Riminucci, M; Dazzi, F; Biondi, A; Serafini, M
Bath PUVA therapy in pediatric patients with drug-resistant cutaneous graft-versus-host disease
2001 Bonanomi, S; Balduzzi, A; Tagliabue, A; Biagi, E; Rovelli, A; Corti, P; Crippa, D; Uderzo, C