Publications by authors named "Michaela Calvillo"

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Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia.
Gianluca Dell'Orso, Tommaso Passarella, Serena Cappato, Enrico Cappelli, Stefano Regis, Michaela Calvillo

Int J Mol Sci· July 2025

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Severe Lactic Acidosis Caused by Thiamine Deficiency in a Child with Relapsing Acute Lymphoblastic Leukemia: A Case Report.
Francesco Baldo, Enrico Drago, Daniela Nisticò, Silvia Buratti, Michaela Calvillo

Children (Basel)· September 2023

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Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?
Elena Palmisani, Maurizio Miano, Alice Grossi, Marina Lanciotti, Michela Lupia, Michaela Calvillo

Hemasphere· March 2023

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Underlying CTLA4 Deficiency in a Patient With Juvenile Idiopathic Arthritis and Autoimmune Lymphoproliferative Syndrome Features Successfully Treated With Abatacept-A Case Report.
Marta Mazzoni, Gianluca Dell'Orso, Alice Grossi, Isabella Ceccherini, Stefania Viola, Michaela Calvillo

J Pediatr Hematol Oncol· November 2021

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Unusual Late-onset Enteropathy in a Patient With Lipopolysaccharide-responsive Beige-like Anchor Protein Deficiency.
Rosario Maggiore, Alice Grossi, Francesca Fioredda, Elena Palmisani, Paola Terranova, Michaela Calvillo

J Pediatr Hematol Oncol· November 2020

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FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene.
Maurizio Miano, Enrico Cappelli, Agnese Pezzulla, Roberta Venè, Alice Grossi, Michaela Calvillo

Br J Haematol· November 2019

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Clinical features and therapeutic challenges of cytopenias belonging to alps and alps-related (ARS) phenotype.
Elena Palmisani, Maurizio Miano, Concetta Micalizzi, Michaela Calvillo, Filomena Pierri

Br J Haematol· March 2019

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Sirolimus as a rescue therapy in children with immune thrombocytopenia refractory to mycophenolate mofetil.
Maurizio Miano, Gioacchino Andrea Rotulo, Elena Palmisani, Mariateresa Giaimo, Francesca Fioredda, Michaela Calvillo

Am J Hematol· July 2018

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Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.
Roberta Bottega, Elena Nicchia, Enrico Cappelli, Silvia Ravera, Daniela De Rocco, Michaela Calvillo

Haematologica· March 2018

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Long-term use of pegfilgrastim in children with severe congenital neutropenia: clinical and pharmacokinetic data.
Francesca Fioredda, Tiziana Lanza, Federica Gallicola, Francesca Riccardi, Marina Lanciotti, Michaela Calvillo

Blood· October 2016

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Mycophenolate mofetil and Sirolimus as second or further line treatment in children with chronic refractory Primitive or Secondary Autoimmune Cytopenias: a single centre experience.
Maurizio Miano, Maria Scalzone, Katia Perri, Elena Palmisani, Ilaria Caviglia, Michaela Calvillo

Br J Haematol· October 2015

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Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow Transplantation.
Francesca Fioredda, Simona Iacobelli, Anja van Biezen, Bobby Gaspar, Phil Ancliff, Michaela Calvillo

Blood· October 2015

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Lethal sepsis and malignant transformation in severe congenital neutropenia: report from the Italian Neutropenia Registry.
Francesca Fioredda, Michaela Calvillo, Marina Lanciotti, Maria Giuseppina Cefalo, Fabio Tucci

Pediatr Blood Cancer· June 2015

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Sirolimus for the treatment of multi-resistant autoimmune haemolytic anaemia in children.
Maurizio Miano, Michaela Calvillo, Elena Palmisani, Francesca Fioredda, Concetta Micalizzi

Br J Haematol· November 2014

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Sirolimus as maintenance treatment in an infant with life-threatening multiresistant pure red cell anemia/autoimmune hemolytic anemia.
Maurizio Miano, Vincenzo Poggi, Laura Banov, Francesca Fioredda, Concetta Micalizzi, Michaela Calvillo

J Pediatr Hematol Oncol· April 2014

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Role of management strategies in reducing mortality from invasive fungal disease in children with cancer or receiving hemopoietic stem cell transplant: a single center 30-year experience.
Elio Castagnola, Francesca Bagnasco, Loredana Amoroso, Ilaria Caviglia, Silvia Caruso, Michaela Calvillo

Pediatr Infect Dis J· March 2014

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Infectious complications in children with severe congenital, autoimmune or idiopathic neutropenia: a retrospective study from the Italian Neutropenia Registry.
Francesca Fioredda, Michaela Calvillo, Oriana Burlando, Francesca Riccardi, Ilaria Caviglia

Pediatr Infect Dis J· April 2013

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Diagnostic potential of hepcidin testing in pediatrics.
Giuliana Cangemi, Angela Pistorio, Maurizio Miano, Marco Gattorno, Maura Acquila, Michaela Calvillo

Eur J Haematol· April 2013

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Clofarabine, cyclophosphamide and etoposide for the treatment of relapsed or resistant acute leukemia in pediatric patients.
Maurizio Miano, Angela Pistorio, Maria C Putti, Carlo Dufour, Chiara Messina, Michaela Calvillo

Leuk Lymphoma· September 2012

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Congenital and acquired neutropenias consensus guidelines on therapy and follow-up in childhood from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).
Francesca Fioredda, Michaela Calvillo, Sonia Bonanomi, Tiziana Coliva, Fabio Tucci

Am J Hematol· February 2012

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B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen.
Irene Puga, Montserrat Cols, Carolina M Barra, Bing He, Linda Cassis, Michaela Calvillo

Nat Immunol· December 2011

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Congenital and acquired neutropenia consensus guidelines on diagnosis from the Neutropenia Committee of the Marrow Failure Syndrome Group of the AIEOP (Associazione Italiana Emato-Oncologia Pediatrica).
Francesca Fioredda, Michaela Calvillo, Sonia Bonanomi, Tiziana Coliva, Fabio Tucci

Pediatr Blood Cancer· July 2011

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Similar favorable outcome of pegfilgrastim overdose in patients with different age and underlying disease.
Carlo Dufour, Barbara Cappelli, Michaela Calvillo, Francesca Fioredda, Rossella Tonelli

Haematologica· April 2010

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Pegfilgrastim in children with severe congenital neutropenia.
Francesca Fioredda, Michaela Calvillo, Marina Lanciotti, Tiziana Lanza, Laura Giunti

Pediatr Blood Cancer· March 2010

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Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia.
Marina Lanciotti, Stefania Indaco, Sonia Bonanomi, Tiziana Coliva, Elena Mastrodicasa, Michaela Calvillo

Haematologica· January 2010

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