CATTONI, ALESSANDRO
CATTONI, ALESSANDRO
DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)
An Attempt to Induce Transient Immunosuppression Pre-erythrocytapheresis in a Girl With Sickle Cell Disease, a History of Severe Delayed Hemolytic Transfusion Reactions and Need for Hip Prosthesis
2013 Cattoni, A; Cazzaniga, G; Perseghin, P; Zatti, G; Gaddi, D; Cossio, A; Biondi, A; Corti, P; Masera, N
The use of recombinant human growth hormone in patients with Mucopolysaccharidoses and growth hormone deficiency: A case series
2019 Cattoni, A; Motta, S; Masera, N; Gasperini, S; Rovelli, A; Parini, R
Phenotypic variability in two siblings with monogenic diabetes due to the same ABCC8 gene mutation
2019 Cattoni, A; Jackson, C; Bain, M; Houghton, J; Wei, C
Unusual association of Mayer-Rokitansky-Küster-Hauser and Sotos syndromes: a case report
2019 Cattoni, A; Albanese, A; Tatton-Brown, K
The Predictive Value of Insulin-Like Growth Factor 1 in Irradiation-Dependent Growth Hormone Deficiency in Childhood Cancer Survivors
2019 Cattoni, A; Clarke, E; Albanese, A
Dexamethasone Stimulation Test in the Diagnostic Work-Up of Growth Hormone Deficiency in Childhood: Clinical Value and Comparison With Insulin-Induced Hypoglycemia
2020 Cattoni, A; Molinari, S; Medici, F; De Lorenzo, P; Valsecchi, M; Masera, N; Adavastro, M; Biondi, A
Final height in growth hormone-deficient childhood cancer survivors after growth hormone therapy
2020 Rodari, G; Cattoni, A; Albanese, A
Hepatic focal nodular hyperplasia after pediatric hematopoietic stem cell transplantation: The impact of hormonal replacement therapy and iron overload
2020 Cattoni, A; Rovelli, A; Prunotto, G; Bonanomi, S; Invernizzi, P; Perego, R; Mariani, A; Balduzzi, 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
The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report
2020 Cattoni, A; Spano, A; Tulone, A; Boneschi, A; Masera, N; Maitz, S; Di Blasio, A; Persani, L; Guizzardi, F; Rossetti, R
Risk factors for endocrine complications in transfusion-dependent thalassemia patients on chelation therapy with deferasirox: a risk assessment study from a multicentre nation-wide cohort
2021 Casale, M; Forni, G; Cassinerio, E; Pasquali, D; Origa, R; Serra, M; Campisi, S; Peluso, A; Renni, R; Cattoni, A; De Michele, E; Allò, M; Poggi, M; Ferrara, F; Di Concilio, R; Sportelli, F; Quarta, A; Putti, M; Notarangelo, L; Sau, A; Ladogana, S; Tartaglione, I; Picariello, S; Marcon, A; Sturiale, P; Roberti, D; Lazzarino, A; Perrotta, S
“Growth patterns in children with mucopolysaccharidosis type I-Hurler after hematopoietic stem cell transplantation: Comparison with untreated patients”
2021 Cattoni, A; Chiaraluce, S; Gasperini, S; Molinari, S; Biondi, A; Rovelli, A; Parini, R
Late Effects After Haematopoietic Stem Cell Transplantation in ALL, Long-Term Follow-Up and Transition: A Step Into Adult Life
2021 Diesch-Furlanetto, T; Gabriel, M; Zajac-Spychala, O; Cattoni, A; Hoeben, B; Balduzzi, A
Biological therapies in monogenic autoinflammatory diseases: Long-term efficacy and safety
2021 Pelagatti, M; Cattoni, A; Rizzari, C
Correction: ABO incompatibile graft management in pediatric transplantation (Bone Marrow Transplantation, (2020), 10.1038/s41409-020-0981-7)
2021 Balduzzi, A; Bonig, H; Jarisch, A; Nava, T; Ansari, M; Cattoni, A; Prunotto, G; Lucchini, G; Krivan, G; Matic, T; Kalwak, K; Yesilipek, A; Ifversen, M; Svec, P; Buechner, J; Vettenranta, K; Meisel, R; Lawitschka, A; Peters, C; Gibson, B; Dalissier, A; Corbacioglu, S; Willasch, A; Dalle, J; Bader, P; Bielorai, B; Cesaro, S; Diesch, T; Kato, K; Gomez, S; Mellgren, K; Palma, J; Rossig, C; Sauer, M; Sedlacek, P; Shaw, P; Schultz, K; Stein, J; Tayfun, G; Turkiewicz, D; Wachowiak, J
A novel germline mutation of ada2 gene in two “discordant” homozygous female twins affected by adenosine deaminase 2 deficiency: Description of the bone-related phenotype
2021 Vai, S; Marin, E; Cosso, R; Saettini, F; Bonanomi, S; Cattoni, A; Chiodini, I; Persani, L; Falchetti, A
Serum anti-Müllerian hormone as a marker of ovarian reserve after cancer treatment and/or hematopoietic stem cell transplantation in childhood: proposal for a systematic approach to gonadal assessment
2021 Molinari, S; Parissone, F; Evasi, V; De Lorenzo, P; Valsecchi, M; Cesaro, S; Fraschini, D; Sangalli, R; Cacace, G; Biondi, A; Balduzzi, A; Cattoni, A
Primary immunodeficiencies, autoimmune hyperthyroidism, coeliac disease and systemic lupus erythematosus in childhood immune thrombocytopenia
2021 Saettini, F; Cattoni, A; Redaelli, M; Silvestri, D; Ferrari, G; Biondi, A; Jankovic, M; Spinelli, M
ABO incompatibile graft management in pediatric transplantation
2021 Balduzzi, A; Bönig, H; Järisch, A; Nava, T; Ansari, M; Cattoni, A; Prunotto, G; Lucchini, G; Krivan, G; Matic, T; Kalwak, K; Yesilipek, A; Ifversen, M; Svec, P; Büchner, J; Vettenranta, K; Meisel, R; Lawitschka, A; Peters, C; Gibson, B; Dalissier, A; Corbacioglu, S; Willasch, A; Dalle, J; Bader, P
Hormonal replacement therapy in adolescents and young women with chemo- or radio-induced premature ovarian insufficiency: Practical recommendations
2021 Cattoni, A; Parissone, F; Porcari, I; Molinari, S; Masera, N; Franchi, M; Cesaro, S; Gaudino, R; Passoni, P; Balduzzi, A