Agranulocytosis due to deferiprone: a case report with cytomorphological and functional bone marrow examination

por Masera, Nicoletta, Tavecchia, Luisa, Longoni, Daniela Valentina, Maglia, Oscar, Biondi, Andrea, Masera, Giuseppe
Publicado 2011

Optimal response to thalidomide in a patient with thalassaemia major resistant to conventional therapy

por Masera, Nicoletta, Tavecchia, Luisa, Capra, Marietta, Cazzaniga, Giovanni, Vimercati, Chiara, Pozzi, Lorena, Biondi, Andrea, Masera, Giuseppe
Publicado 2010

Optimal response to thalidomide in a patient with thalassaemia major resistant to conventional therapy

por Masera, Nicoletta, Tavecchia, Luisa, Capra, Marietta, Cazzaniga, Giovanni, Vimercati, Chiara, Pozzi, Lorena, Biondi, Andrea, Masera, Giuseppe
Publicado 2010

Organizing national responses for rare blood disorders: the Italian experience with sickle cell disease in childhood

por Colombatti, Raffaella, Perrotta, Silverio, Samperi, Piera, Casale, Maddalena, Masera, Nicoletta, Palazzi, Giovanni, Sainati, Laura, Russo, Giovanna
Publicado en Orphanet J Rare Dis (2013)

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 fo...

por Cattoni, Alessandro, Cazzaniga, Giovanni, Perseghin, Paolo, Zatti, Giovanni, Gaddi, Diego, Cossio, Andrea, Biondi, Andrea, Corti, Paola, Masera, Nicoletta
Publicado 2013

Dexamethasone Stimulation Test in the Diagnostic Work-Up of Growth Hormone Deficiency in Childhood: Clinical Value and Comparison With Insulin-Induced Hypoglycemia

por Cattoni, Alessandro, Molinari, Silvia, Medici, Francesco, De Lorenzo, Paola, Valsecchi, Maria Grazia, Masera, Nicoletta, Adavastro, Marta, Biondi, Andrea
Publicado en Front Endocrinol (Lausanne) (2020)

Evaluation of Technical Issues in a Pilot Multicenter Newborn Screening Program for Sickle Cell Disease

por Martella, Maddalena, Viola, Giampietro, Azzena, Silvia, Schiavon, Sara, Biondi, Andrea, Basso, Giuseppe, Corti, Paola, Colombatti, Raffaella, Masera, Nicoletta, Sainati, Laura
Publicado en Int J Neonatal Screen (2018)

The Potential Synergic Effect of a Complex Pattern of Multiple Inherited Genetic Variants as a Pathogenic Factor for Ovarian Dysgenesis: A Case Report

por Cattoni, Alessandro, Spano, Alice, Tulone, Anna, Boneschi, Annalisa, Masera, Nicoletta, Maitz, Silvia, Di Blasio, Anna Maria, Persani, Luca, Guizzardi, Fabiana, Rossetti, Raffaella
Publicado en Front Endocrinol (Lausanne) (2020)

Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Associ...

por Ladogana, Saverio, Maruzzi, Matteo, Samperi, Piera, Perrotta, Silverio, Del Vecchio, Giovanni C., Notarangelo, Lucia D., Farruggia, Piero, Verzegnassi, Federico, Masera, Nicoletta, Saracco, Paola, Fasoli, Silvia, Miano, Maurizio, Girelli, Gabriella, Barcellini, Wilma, Zanella, Alberto, Russo, Giovanna
Publicado en Blood Transfus (2017)