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Author/Creator Serafinelli, Jessica

1. Autoimmune neutropenia of childhood secondary to other autoimmune disorders: Data from the Italian neutropenia registry. Issue 9 (7th July 2017)

Authors:
Farruggia, Piero; Puccio, Giuseppe; Fioredda, Francesca; Lanza, Tiziana; Porretti, Laura; Ramenghi, Ugo; Barone, Angelica; Bonanomi, Sonia; Finocchi, Andrea; Ghilardi, Roberta; Ladogana, Saverio; Marra, Nicoletta; Martire, Baldassare; Notarangelo, Lucia Dora; Onofrillo, Daniela; Pillon, Marta; Ru...
Journal:
American journal of hematology
Issue:
Volume 92:Issue 9(2017:Sep.)
Page Start:
E546
Record Type:
Journal Article
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2. Eltrombopag-Induced Acute Liver Failure in a Pediatric Patient: A Pharmacokinetic and Pharmacogenetic Analysis. Issue 4 (August 2018)

Authors:
Marano, Marco; Serafinelli, Jessica; Cairoli, Sara; Martinelli, Diego; Pisani, Mara; Palumbo, Giuseppe; Cefalo, Maria G.; Cecchetti, Corrado; Di Nardo, Matteo; Falvella, Felicia S.; Goffredo, Bianca M.
Journal:
Therapeutic drug monitoring
Issue:
Volume 40:Issue 4(2018:Aug.)
Page Start:
Record Type:
Journal Article
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3. Idiopathic neutropenia of infancy: Data from the Italian Neutropenia Registry. Issue 2 (18th December 2018)

Authors:
Farruggia, Piero; Fioredda, Francesca; Puccio, Giuseppe; Onofrillo, Daniela; Russo, Giovanna; Barone, Angelica; Bonanomi, Sonia; Boscarol, Gianluca; Finocchi, Andrea; Ghilardi, Roberta; Giordano, Paola; Ladogana, Saverio; Lassandro, Giuseppe; Luti, Laura; Lanza, Tiziana; Mandaglio, Rosalba; Marra...
Journal:
American journal of hematology
Issue:
Volume 94:Issue 2(2019:Feb.)
Page Start:
216
Record Type:
Journal Article
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4. Late‐onset combined immune deficiency due to LIGIV mutations in a 12‐year‐old patient. Issue 2 (March 2017)

Authors:
Cifaldi, Cristina; Angelino, Giulia; Chiriaco, Maria; Di Cesare, Silvia; Claps, Alessia; Serafinelli, Jessica; Rossi, Paolo; Antoccia, Antonio; Di Matteo, Gigliola; Cancrini, Caterina; De Villartay, Jean Pierre; Finocchi, Andrea
Journal:
Pediatric allergy and immunology
Issue:
Volume 28:Issue 2(2017)
Page Start:
203
Record Type:
Journal Article
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5. Next-Generation Sequencing Reveals A JAGN1 Mutation in a Syndromic Child With Intermittent Neutropenia. Issue 4 (May 2019)

Authors:
Cifaldi, Cristina; Serafinelli, Jessica; Petricone, Davide; Brigida, Immacolata; Di Cesare, Silvia; Di Matteo, Gigliola; Chiriaco, Maria; De Vito, Rita; Palumbo, Giuseppe; Rossi, Paolo; Palma, Paolo; Cancrini, Caterina; Aiuti, Alessandro; Finocchi, Andrea
Journal:
Journal of pediatric hematology/oncology
Issue:
Volume 41:Issue 4(2019)
Page Start:
Record Type:
Journal Article
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