Paolo D'Angelo

Scopus Publications

Diagnostic Delay and Survival in Pediatric Rhabdomyosarcoma: Is Time a Critical Factor?
Maria C. Affinita, Stefano Chiaravalli, Giuseppe M. Milano, Ida Russo, Katia Perruccio, et al.
Journal of Pediatric Hematology Oncology, 2026
Background: Timely diagnosis is considered critical in pediatric oncology to optimize treatment outcomes, as delays may impact tumor extension and prognosis. We aimed to assess whether the time to diagnosis and treatment initiation for pediatric patients with rhabdomyosarcoma (RMS) improved over time in Italy and whether longer delays were associated with tumor extension and prognosis. Methods: We analyzed 749 pediatric patients diagnosed with RMS between 1996 and 2016. Diagnostic interval (DI) was defined as the number of days from symptom onset to diagnosis, while treatment interval (TI) was defined as the time from symptom onset to treatment initiation. DI was correlated with tumor characteristics at diagnosis, and TI was analyzed in relation to survival, using Kaplan-Meier analysis. Results: The median DI was 32 days, showing a decreasing trend from 39.5 days in 1996 to 2000 to 30 days in 2011 to 2016. A longer DI was associated with age, unfavorable histology, and metastatic disease in univariate analysis, but these were not confirmed in multivariate analysis. The median TI was 48 days. Five-year event-free survival (EFS) and overall survival (OS) were 59.7% and 69.3%. In multivariate analysis, prognosis was negatively associated with age at diagnosis, unfavorable site, nodal involvement, and metastatic disease. TI was not associated with survival. Conclusions: In our national cohort, the time from symptom onset to diagnosis showed a trend toward shortening in recent years. While a timely diagnosis can provide clarity on the child’s condition and potentially reduce parental anxiety, it does not substantially impact tumor characteristics or patient outcomes.
Metachronous Bilateral Adrenal Neuroblastoma: A Case Report and Literature Review
Serena Tropia, Angela Guarina, Giulia Angela Restivo, Fabrizio Di Francesco, Angela Trizzino, et al.
Journal of Pediatric Hematology Oncology, 2024
A baby presented with a large right adrenal mass, multiple hepatic lesions and diffuse bone marrow infiltration when she was just over 1 month old. After needle biopsy and a histologic definition of neuroblastoma, she underwent chemotherapy and a subsequent complete resection. Three years after diagnosis, a large left adrenal localized mass was detected. The patient underwent complete surgical excision, and a diagnosis of poorly differentiated neuroblastoma with multiple lymph nodes involvement was defined. Adjuvant chemotherapy was initiated. To our knowledge, it is the first case report of metachronous bilateral adrenal neuroblastomas harboring completely different genetic expression profiles.
Role of 18F-Fluorodeoxyglucose Positron Emission Tomography in Children With Germ Cell Tumor After Chemotherapy
Maria Debora De Pasquale, Paolo D’Angelo, Alessandro Crocoli, Stefano G. Vallero, Patrizia Bertolini, et al.
Journal of Pediatric Hematology Oncology, 2024
Background/Aim: 18F-fluoro-2-deoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) is a diagnostic tool widely used in adult oncology and some pediatric oncological settings. There are no established recommendations for the use of this imaging modality in pediatric malignant germ cell tumors (mGCT), however. Our aim is to evaluate the role of 18F-FDG PET/CT in the restaging of mGCT after chemotherapy in children and adolescents. Methods: We retrospectively reviewed patients with mGCT treated in Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) centers who underwent 18F-FDG PET/CT between 2011 and 2021. Results: Seventeen patients (median age 13 y) were included in the study. In 14 patients, 18F-FDG PET/CT was performed at diagnosis; 12 showed pathologic uptake. The 2 18F-FDG PET/CT negative cases were histologically defined as yolk sac tumor (YST) and mixed (chorioncarcinoma, YST). Nine of the 12 patients who had pathologic 18F-FDG PET/CT at diagnosis repeated the examination after neoadjuvant chemotherapy, before, second look surgery. In 5 cases, no pathologic uptake was evident. Histology showed necrosis alone in 4 cases and necrosis and mature teratoma in 1. In 3 of the 6 cases with pathologic uptake (2 of 6 patients did not perform the examination at diagnosis), histology showed persistence of malignant component, whereas in the remaining 3 cases, necrosis and mature teratoma were present. Conclusion: In our review of a series of children with mGCT, 18F-FDG PET/CT after neoadjuvant chemotherapy showed 1 of 5 false negatives and was unable to discriminate between residual malignant component and mature teratoma.
Should we reduce routine surveillance imaging in pediatric germ cell tumors?
Monica Terenziani, Francesco Barretta, Giovanna Gattuso, Gianni Bisogno, Massimo Conte, et al.
Pediatric Blood and Cancer, 2023
This paper retrospectively investigated the site and the detection method of relapses in children and adolescents with malignant germ cell tumors enrolled in the TCGM‐AIEOP‐2004 Study and subsequently developed a relapse, in order to evaluate a possible reduction in radiological exposure during follow‐up. Including all malignant cases, serum tumor markers identified a relapse in more than 70% and, according to the selection criteria published by Children Oncology Group in 2018, in more than 90% of cases. These results confirm the importance of serum tumor markers as a relapse detection method, with possible reduction of radiology exams in specific subgroups.
Role of centers with different patient volumes in the management of rhabdomyosarcoma. An analysis by the Italian Pediatric Soft Tissue Sarcoma Committee
Gianni Bisogno, Giovanna Congiu, Maria Carmen Affinita, Giuseppe Maria Milano, Ilaria Zanetti, et al.
Pediatric Blood and Cancer, 2021
The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers’ experience (based on the number of patients treated) in their management of patients with RMS.
Rasburicase-induced Methemoglobinemia: A Case Report and Literature Review
Ilaria Pirrone, Piero Farruggia, Francesca Cacciatore, Antonino Giambona, Angela Guarina, et al.
Journal of Pediatric Hematology Oncology, 2021
Rasburicase is a recombinant urate oxidase enzyme indicated for tumor lysis syndrome, a potential life-threatening oncologic emergency that occurs most commonly during initial chemotherapy for hematological malignancies. As a result of the defects in the physiological antioxidant pathway, erythrocytes of patients with glucose-6-phosphate dehydrogenase deficiency are not protected against the oxidizing stress exerted by hydrogen peroxide generated with the administration of rasburicase. The authors report a 14-year-old patient, diagnosed with T-cell acute lymphoblastic leukemia, who developed methemoglobinemia and hemolytic anemia with low oxygen saturation after starting steroids, hyperhydratation, and rasburicase administration. The complications resolved with supportive therapy only.
Extra-appendicular neuroendocrine tumors: A report from the TREP project (2000-2020)
Calogero Virgone, Andrea Ferrari, Stefano Chiaravalli, Maria Debora De Pasquale, Alessandro Inserra, et al.
Pediatric Blood and Cancer, 2021
Extra‐appendicular neuroendocrine tumors (NETs) are very rare tumors. While diagnostic and therapeutic guidelines are well established for adults, data on children and adolescents are lacking.
Malignant sacrococcygeal germ cell tumors in childhood: The Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) experience
Paolo D'Angelo, Maria Debora De Pasquale, Francesco Barretta, Maria Carmen Affinita, Massimo Conte, et al.
Pediatric Blood and Cancer, 2021
To evaluate clinical features at diagnosis, prognostic factors, and outcomes of malignant sacrococcygeal germ cell tumors (SC‐GCTs) in patients enrolled in the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) TCG 2004 protocol.
Pheochromocytomas and paragangliomas in children: Data from the Italian Cooperative Study (TREP)
Calogero Virgone, Marina Andreetta, Stefano Avanzini, Stefano Chiaravalli, Maria Debora De Pasquale, et al.
Pediatric Blood and Cancer, 2020
Pheochromocytomas (PCs) are neuroendocrine tumors arising from the chromaffin cells of the adrenal gland, and paragangliomas (PGLs) are their extra‐adrenal counterparts arising from ganglia along the sympathetic/parasympathetic chain. Surgery is the cornerstone of treatment. A sporatic or inherited germline mutation is commonly associated.
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Medico E Bambino, 2020
Genomic coamplification of CDK4/MDM2/FRS2 is associated with very poor prognosis and atypical clinical features in neuroblastoma patients
Loredana Amoroso, Marzia Ognibene, Martina Morini, Massimo Conte, Andrea Di Cataldo, et al.
Genes Chromosomes and Cancer, 2020
Salvage treatment for children with relapsed/refractory germ cell tumors: The Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) experience
Maria Debora De Pasquale, Paolo D'Angelo, Alessandro Crocoli, Renata Boldrini, Massimo Conte, et al.
Pediatric Blood and Cancer, 2020
The relation between maternal locus of control and coping styles of pediatric leukemia patients during treatment
Concetta Polizzi, Giovanna Perricone, Valentina Fontana, Paolo D'Angelo, Momcilo Jankovic, et al.
Pediatric Reports, 2020
Late mortality and causes of death among 5-year survivors of childhood cancer diagnosed in the period 1960–1999 and registered in the Italian Off-Therapy Registry
Francesca Bagnasco, Silvia Caruso, Anita Andreano, Maria Grazia Valsecchi, Momcilo Jankovic, et al.
European Journal of Cancer, 2019
Stage 4 s neuroblastoma: Features, management and outcome of 268 cases from the Italian Neuroblastoma Registry
Bruno De Bernardi, Andrea Di Cataldo, Alberto Garaventa, Paolo Massirio, Elisabetta Viscardi, et al.
Italian Journal of Pediatrics, 2019
Microenvironment in neuroblastoma: Isolation and characterization of tumor-derived mesenchymal stromal cells
Gloria Pelizzo, Veronica Veschi, Melissa Mantelli, Stefania Croce, Vincenzo Di Benedetto, et al.
BMC Cancer, 2018
Malignant testicular germ cell tumors in children and adolescents: The AIEOP (Associazione Italiana Ematologia Oncologia Pediatrica) protocol
Monica Terenziani, Maria D. De Pasquale, Gianni Bisogno, Davide Biasoni, Renata Boldrini, et al.
Urologic Oncology Seminars and Original Investigations, 2018
Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility
Oncotarget, 2018
Salvage rates and prognostic factors after relapse in children and adolescents with malignant peripheral nerve sheath tumors
Luca Bergamaschi, Gianni Bisogno, Carla Manzitti, Paolo D'Angelo, Giuseppe Maria Milano, et al.
Pediatric Blood and Cancer, 2018
Factors possibly affecting prognosis in children with Wilms’ tumor diagnosed before 24 months of age: A report from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) Wilms Tumor Working Group
Paolo D'Angelo, Andrea Di Cataldo, Monica Terenziani, Gianni Bisogno, Paola Collini, et al.
Pediatric Blood and Cancer, 2017
Front-line window therapy with cisplatin in patients with primary disseminated Ewing sarcoma: A study by the Associazione Italiana di Ematologia ed Oncologia Pediatrica and Italian Sarcoma Group
Roberto Luksch, Giovanni Grignani, Paolo D'Angelo, Arcangelo Prete, Nadia Puma, et al.
Pediatric Blood and Cancer, 2017
Gastrointestinal tract carcinoma in pediatric and adolescent age: The Italian TREP project experience
Alice Indini, Gianni Bisogno, Giovanni Cecchetto, Marco Vitellaro, Stefano Signoroni, et al.
Pediatric Blood and Cancer, 2017
Malignant ovarian germ cell tumors in pediatric patients: The AIEOP (Associazione Italiana Ematologia Oncologia Pediatrica) study
M. Terenziani, G. Bisogno, R. Boldrini, G. Cecchetto, M. Conte, et al.
Pediatric Blood and Cancer, 2017
Results of the Third AIEOP Cooperative Protocol on Wilms Tumor (TW2003) and Related Considerations
Filippo Spreafico, Davide Biasoni, Salvatore Lo Vullo, Lorenza Gandola, Paolo D’Angelo, et al.
Journal of Urology, 2017
Ante situm liver resection with inferior vena cava replacement under hypothermic cardiopolmunary bypass for hepatoblastoma: Report of a case and review of the literature
Roberta Angelico, Annalisa Passariello, Michele Pilato, Tommaso Cozzolino, Marcello Piazza, et al.
International Journal of Surgery Case Reports, 2017
Perioperative management of hypertensive neuroblastoma: A study from the Italian Group of Pediatric Surgical Oncologists (GICOP)
Luca Pio, Stefano Avanzini, Girolamo Mattioli, Giuseppe Martucciello, Angela Rita Sementa, et al.
Journal of Pediatric Surgery, 2017
Prognostic factors in children undergoing salvage surgery for bladder/prostate rhabdomyosarcoma
Lorenzo Angelini, Gianni Bisogno, Rita Alaggio, Giovanni Scarzello, Luisa Santoro, et al.
Journal of Pediatric Urology, 2016
Spiritual support for adolescent cancer patients: A survey of pediatric oncology centers in Italy and Spain
Tullio Proserpio, Laura Veneroni, Matteo Silva, Alvaro Lassaletta, Rosalia Lorenzo, et al.
Tumori, 2016
Mediastinal Germ Cell Tumors in Pediatric Patients: A Report From the Italian Association of Pediatric Hematology and Oncology
Maria Debora De Pasquale, Alessandro Crocoli, Massimo Conte, Paolo Indolfi, Paolo D'Angelo, et al.
Pediatric Blood Cancer, 2016
Severe lower limb ischemia by massive arterial thrombosis revealing an acute myeloid leukemia needing for leg amputation: Clinical and emotional aspects related to the communication with the patient and his family
Paolo D'Angelo, Calogero Taormina, Clara Mosa, Floriana Di Marco, Fabrizio Valentino, et al.
Pediatric Reports, 2016
Bone Sarcomas in Children and Adolescents
Floriana Di Marco, Fabrizia Ferraro, Clara Mosa, Angela Trizzino, Serena Tropia, et al.
Journal of Pediatric Biochemistry, 2015
Non-hodgkin lymphoma in children with an associated inherited condition: A retrospective analysis of the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP)
Maurizio Aricò, Lara Mussolin, Elisa Carraro, Salvatore Buffardi, Nicola Santoro, et al.
Pediatric Blood and Cancer, 2015
Genetic abnormalities in adolescents and young adults with neuroblastoma: A report from the Italian Neuroblastoma group
Katia Mazzocco, Raffaella Defferrari, Angela Rita Sementa, Alberto Garaventa, Luca Longo, et al.
Pediatric Blood and Cancer, 2015
Long-term results of the AIEOP LNH-97 protocol for childhood lymphoblastic lymphoma
Marta Pillon, Maurizio Aricò, Lara Mussolin, Elisa Carraro, Valentino Conter, et al.
Pediatric Blood and Cancer, 2015
Mature and immature teratoma: A report from the second Italian pediatric study
Monica Terenziani, Paolo D'Angelo, Alessandro Inserra, Renata Boldrini, Gianni Bisogno, et al.
Pediatric Blood and Cancer, 2015
Management and follow-up of urothelial neoplasms of the bladder in children: A report from the TREP project
Daniela Di Carlo, Andrea Ferrari, Katia Perruccio, Paolo D'Angelo, Anna Maria Fagnani, et al.
Pediatric Blood and Cancer, 2015
Acute respiratory distress syndrome associated with tumor lysis syndrome in a child with acute lymphoblastic leukemia
Alessandra Macaluso, Selene Genova, Silvio Maringhini, Giancarlo Coffaro, Ottavio Ziino, et al.
Pediatric Reports, 2015
Coping strategies and locus of control in childhood leukemia: A multi-center research
Concetta Polizzi, Valentina Fontana, Giovanna Perricone, Paolo D'Angelo, Momcilo Jankovic, et al.
Pediatric Reports, 2015
Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney
Annalisa Astolfi, Fraia Melchionda, Daniela Perotti, Maura Fois, Valentina Indio, et al.
Oncotarget, 2015
Pediatric gastrointestinal PEComas: A diagnostic challenge
Marco Pizzi, Ida di Lorenzo, Emanuele S. d'Amore, Paolo D'Angelo, Rita Alaggio
Pediatric and Developmental Pathology, 2014
Treatment of human papillomavirus infection with interferon alpha and ribavirin in a patient with acquired aplastic anemia
Clara Mosa, Antonino Trizzino, Angela Trizzino, Floriana Di Marco, Paolo D’Angelo, et al.
International Journal of Infectious Diseases, 2014
FIP1L1-PDGFRα-positive hypereosinophilic syndrome in childhood: A case report and review of literature
Piero Farruggia, Emilia Giugliano, Delia Russo, Angela Trizzino, Roberta Lorenzatti, et al.
Journal of Pediatric Hematology Oncology, 2014
Poikiloderma with neutropenia: A case report and review of the literature
Piero Farruggia, Stefania Indaco, Carlo Dufour, Tiziana Lanza, Clara Mosa, et al.
Journal of Pediatric Hematology Oncology, 2014
Dramatic response to cisplatin window therapy in a boy with advanced metastatic ewing sarcoma
Antonino Trizzino, Ottavio Ziino, Antonina Parafioriti, Marta Podda, Serena Tropia, et al.
Journal of Pediatric Hematology Oncology, 2013
MPL W515L mutation in pediatric essential thrombocythemia
Piero Farruggia, Paolo D'Angelo, Maria La Rosa, Nunzia Scibetta, Giuseppe Santangelo, et al.
Pediatric Blood and Cancer, 2013
Synchronous bilateral Wilms tumor: A report from the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP)
Paolo Indolfi, Alessandro Jenkner, Monica Terenziani, Alessandro Crocoli, Annalisa Serra, et al.
Cancer, 2013
Loss of heterozygosity analysis at different chromosome regions in wilms tumor confirms 1p allelic loss as a marker of worse prognosis: A study from the Italian association of pediatric hematology and oncology
Filippo Spreafico, Beatrice Gamba, Luigi Mariani, Paola Collini, Paolo D'Angelo, et al.
Journal of Urology, 2013
The spectrum of non-classical Diamond-Blackfan anemia: A case of late beginning transfusion dependency associated to a new RPL5 mutation
Piero Farruggia, Paola Quarello, Emanuela Garelli, Olivia Paolicchi, Giovanni Battista Ruffo, et al.
Pediatric Reports, 2012
Prognostic value of ferritin, neuron-specific enolase, lactate dehydrogenase, and urinary and plasmatic catecholamine metabolites in children with neuroblastoma
Maria Valeria Corrias, Cangemi, Reggiardo, Barco, Barbagallo, et al.
Oncotargets and Therapy, 2012
Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse
Daniela Perotti, Filippo Spreafico, Federica Torri, Beatrice Gamba, Pio D'Adamo, et al.
Genes Chromosomes and Cancer, 2012
Vocal cord palsy after vincristine treatment in a child and the inefficacy of glutamic acid in the prevention of relapse: A case report
Piero Farruggia, Serena Tropia, Sonia Cannella, Giuseppa Bruno, Gaspare Oddo, et al.
Journal of Medical Case Reports, 2012
A prospective protocol for nasopharyngeal carcinoma in children and adolescents: The Italian Rare Tumors in Pediatric Age (TREP) project
Michela Casanova, Gianni Bisogno, Lorenza Gandola, Giovanni Cecchetto, Andrea Di Cataldo, et al.
Cancer, 2012
Simultaneous diagnosis of acute lymphoblastic leukemia and peripheral neuroblastic tumor in a child
Paolo D'Angelo, Antonella Grigoli, Angela Rita Sementa, Serena Tropia, Rita Alaggio, et al.
Journal of Pediatric Hematology Oncology, 2012
Heterogeneity of disease classified as stage III in Wilms tumor: A report from the associazione Italiana Ematologia Oncologia Pediatrica (AIEOP)
Filippo Spreafico, Lorenza Gandola, Paolo D’Angelo, Monica Terenziani, Paola Collini, et al.
International Journal of Radiation Oncology Biology Physics, 2012
Effectiveness of cyclosporine and mycophenolate mofetil in a child with refractory evans syndrome
Piero Farruggia, Alessandra Macaluso, Serena Tropia, Selene Genova, Olivia Paolicchi, et al.
Pediatric Reports, 2011
Castleman's disease in childhood: Report of three cases and review of the literature
Piero Farruggia, Antonino Trizzino, Nunzia Scibetta, Giovanni Cecchetto, Patrizia Guerrieri, et al.
Italian Journal of Pediatrics, 2011
Hepatopathy-thrombocytopenia syndrome (HTS) after actinomycin-D therapy: Report of three cases and review of the literature
Piero Farruggia, Alessandra Macaluso, Serena Tropia, Floriana Di Marco, Delia Russo, et al.
Pediatric Hematology and Oncology, 2011
Breast metastases in children and adolescents with rhabdomyosarcoma: Experience of the Italian soft tissue sarcoma committee
Paolo D'Angelo, Modesto Carli, Andrea Ferrari, Carla Manzitti, Rossella Mura, et al.
Pediatric Blood and Cancer, 2010
Focal nodular hyperplasia of the liver: an unusual association with diabetes mellitus in a child and review of literature.
Piero Farruggia, Rita Alaggio, Francesca Cardella, Serena Tropia, Antonino Trizzino, et al.
Italian Journal of Pediatrics, 2010
When primary immunodeficiency must be suspected
Area Pediatrica, 2010
Hodgkin lymphoma and nephrotic syndrome in childhood
Piero Farruggia, Antonino Trizzino, Silvio Maringhini, Antonella Grigoli, Chiara Sapia, et al.
Indian Journal of Pediatrics, 2010
Severe polyuria and polydipsia in hyponatremic-hypertensive syndrome associated with Wilms tumor
Paolo D'Angelo, Serena Catania, Giusy Zirilli, Paola Collini, Serena Tropia, et al.
Pediatric Blood and Cancer, 2010
Improved survival of children with neuroblastoma between 1979 and 2005: A report of the Italian neuroblastoma registry
Riccardo Haupt, Alberto Garaventa, Claudio Gambini, Stefano Parodi, Giuliana Cangemi, et al.
Journal of Clinical Oncology, 2010
Pancreatic tumors in children and adolescents: The Italian TREP project experience
Patrizia Dall'Igna, Giovanni Cecchetto, Gianni Bisogno, Massimo Conte, Pierluigi Lelli Chiesa, et al.
Pediatric Blood and Cancer, 2010
Teratoma with a malignant somatic component in pediatric patients: The Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP) experience
Monica Terenziani, Paolo D'Angelo, Gianni Bisogno, Renata Boldrini, Giovanni Cecchetto, et al.
Pediatric Blood and Cancer, 2010
Sequential high-dose chemotherapy for children with metastatic rhabdomyosarcoma
Gianni Bisogno, Andrea Ferrari, Arcangelo Prete, Chiara Messina, Eleonora Basso, et al.
European Journal of Cancer, 2009
Outcome of children with neuroblastoma after progression or relapse. A retrospective study of the Italian neuroblastoma registry
Alberto Garaventa, Stefano Parodi, Bruno De Bernardi, Daniela Dau, Carla Manzitti, et al.
European Journal of Cancer, 2009
Hyperosinophilic syndrome in childhood: Clinical and molecular features of two cases
Piero Farruggia, Paolo D'Angelo, Antonio Acquaviva, Antonino Trizzino, Fabio Tucci, et al.
Pediatric Hematology and Oncology, 2009
Treatment of high-risk relapsed Wilms tumor with dose-intensive chemotherapy, marrow-ablative chemotherapy, and autologous hematopoietic stem cell support: Experience by the Italian Association of Pediatric Hematology and Oncology
Filippo Spreafico, Gianni Bisogno, Paola Collini, Alessandro Jenkner, Lorenza Gandola, et al.
Pediatric Blood and Cancer, 2008
Synovial sarcoma of the neck in a child: A multidisciplinary approach
Piero Farruggia, Paolo D’Angelo, Manlio Lo Cascio, Luigi Solazzo, Paolo Montemaggi, et al.
Pediatric Hematology and Oncology, 2008
Synovial sarcoma of children and adolescents: The prognostic role of axial sites
Andrea Ferrari, Gianni Bisogno, Rita Alaggio, Giovanni Cecchetto, Paola Collini, et al.
European Journal of Cancer, 2008
Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith - Wiedemann syndrome and Wilms' tumour
F. Cerrato, A. Sparago, G. Verde, A. De Crescenzo, V. Citro, et al.
Human Molecular Genetics, 2008
Epilepsy and cancer in pediatric age
Bollettino Lega Italiana Contro L Epilessia, 2008
Soft-tissue sarcomas in children and adolescents with neurofibromatosis type 1
Andrea Ferrari, Gianni Bisogno, Alessandra Macaluso, Michela Casanova, Paolo D'Angelo, et al.
Cancer, 2007
Mature and immature teratomas: Results of the first paediatric Italian study
Margherita Lo Curto, Paolo D’Angelo, Giovanni Cecchetto, Catherine Klersy, Patrizia Dall’Igna, et al.
Pediatric Surgery International, 2007
Pleuropulmonary blastoma: A differential diagnosis of chronic cough. Long-term survival after multimodal aggressive therapy
Italian Journal of Pediatrics, 2006
Neuroblastoma in the first year of life. The Italian contribution to a study of the Internation Society of Paediatric Oncology Europe Neuroblastoma Group
Italian Journal of Pediatrics, 2006
Reversible posterior leukoencephalopathy syndrome: Report of 2 simultaneous cases in children
Paolo D’Angelo, Piero Farruggia, Antonio Lo Bello, Antonino Trizzino, Serena Tropia, et al.
Journal of Pediatric Hematology Oncology, 2006
Congenital hepatic fibrosis: A very uncommon cause of pancytopenia in children
Antonino Trizzino, Piero Farruggia, Delia Russo, Paolo D'Angelo, Serena Tropia, et al.
Journal of Pediatric Hematology Oncology, 2005
The IVADo regimen - A pilot study with ifosfamide, vincristine, actinomycin D, and doxorubicin in children with metastatic soft tissue sarcoma: A pilot study on behalf of the European pediatric soft tissue sarcoma study group
Gianni Bisogno, Andrea Ferrari, Christophe Bergeron, Angela Scagnellato, Arcangelo Prete, et al.
Cancer, 2005
Disseminated neuroblastoma in children older than one year at diagnosis: Comparable results with three consecutive high-dose protocols adopted by the Italian Co-Operatiye Group for Neuroblastoma
Bruno De Bernardi, Brigitte Nicolas, Luca Boni, Paolo Indolfi, Modesto Carli, et al.
Journal of Clinical Oncology, 2003
Brier report: Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) in a girl previously affected by acute lymphoblastic leukemia
Michaela R. Allen, Vito Ninfo, Alessandra Viglio, Paolo D'Angelo, Marco Paulli, et al.
Medical and Pediatric Oncology, 2001
Fibroma of the left ventricle in a patient with Sotos syndrome
Marcello Marcì, Ottavio Ziino, Paolo D'Angelo, Giuseppe Miranda, Carlo Pappone, et al.
Echocardiography, 2001
Transfusional hemochromatosis: Quantitative relation of MR imaging pituitary signal intensity reduction to intensity reduction to hypogonadotropic hypogonadism
Gianvincenzo Sparacia, Alberto Iaia, Aurelia Banco, Paolo D'Angelo, Roberto Lagalla
Radiology, 2000
Magnetic resonance imaging of the pituitary gland in patients with secondary hypogonadism due to transfusional hemochromatosis
G Sparacia
Magnetic Resonance Materials in Physics Biology and Medicine, 1999
The breakpoints of a constitutional inversion of chromosome 9 associated with haemophagocytic lymphohistiocytosis are not linked to the disease gene
Maurizio Aricò, Claudia Dellavecchia, Mauro Piantanida, Rita Clementi, Henrik Hasle, et al.
British Journal of Haematology, 1999
Hypogonadotrophic pituitary insufficiency in transfusional hemochromatosis complicating thalassemia major: MR imaging
G. Sparacia, A. Banco, M. Midiri, P. D'Angelo, A. Luca, et al.
Rivista Di Neuroradiologia, 1999
MR imaging of pancreatic changes in patients with transfusion-dependent β-thalassemia major
M Midiri, A Lo Casto, G Sparacia, P D'Angelo, R Malizia, et al.
American Journal of Roentgenology, 1999
Cardiac and pulmonary function abnormalities in thalassemia major patients
Cardiovascular Imaging, 1998
Zinc deficiency and cell-mediated and humoral autoimmunity of insulin- dependent diabetes in thalassemic subjects
Journal of Pediatric Endocrinology and Metabolism, 1998
The heart in β-thalassemia major patients. An MR study
Radiologia Medica, 1998
Serum and fecal pancreatic enzymes in beta-thalassemia major
Giuseppe Montalto, Paolo D’Angelo, Antonio Lo Casto, Antonio Carroccio, Maurizio Soresi, et al.
International Journal of Pancreatology, 1997
High-dose cytosine arabinoside and fractionated total body irradiation as a preparative regimen for the treatment of children with acute lymphoblastic leukemia and Down syndrome by allogeneic bone marrow transplantation
Bone Marrow Transplantation, 1996
Serum Ca 19.9 levels in thalassemia major.
GIUSEPPE MONTALTO, PAOLO DʼANGELO, MARIA TUMMINELLO
Pancreas, 1996
Megaloblastic anemia by alimentary deficiency of folic acid: A clinical case report
Pediatria Oggi Medica E Chirurgica, 1996
Isolated ocular relapse in childhood acute lymphoblastic leukemia during continuing complete remission
Haematologica, 1996
Isolated bilateral otomastoid relapse in a child with acute nonlymphoblastic leukemia
International Journal of Pediatric Hematology Oncology, 1996
Alstrom syndrome: A clinical case report
Rivista Italiana Di Pediatria, 1995
Efficacy of prolonged low-dose steroid treatment in a child with idiopathic hypereosinophilic syndrome: A case report
Carmelo Rizzari, Valentino Conter, Paolo D'Angelo, Angelo Cantù-Rajnoldi, Giuseppe Masera
Pediatric Hematology and Oncology, 1995
Leukemic ophthalmopathy in children: Results of a polycentric study in 59 cases
Haematologica, 1994
Thyroid disease in patients with thalassemia
Haematologica, 1994
Leukemic ophthalmopathy: A report of 21 pediatric cases
M. Lo Curto, P. D'Angelo, F. Lumia, G. Provenzano, A. Zingone, et al.
Medical and Pediatric Oncology, 1994
Severe osteoporosis and multiple vertebral collapses in a child during treatment for B-all
Paolo D’Angelo, Valentino Conter, Gianluigi Di Chiara, Carmelo Rizzari, Antonio Memeo, et al.
Acta Haematologica, 1993
Isolated breast relapse after allogeneic bone marrow transplantation for childhood acute lymphoblastic leukemia
Valentino Conter, Paolo D'Angelo, Attilio Rovelli, Cornelio Uderzo, Momcilo Jankovic, et al.
Medical and Pediatric Oncology, 1992
Lineage switch in a childhood t-cell acute lymphoblastic leukemia
Rosamaria Mura, Paolo D'angelo, Carmelo Rizzari, Andrea Biondi, Giovanni Giudici, et al.
Pediatric Hematology and Oncology, 1992
Acute lymphoblastic leukaemia in a child with cystic fibrosis
Haematologica, 1992
Central venous catheter-related complications after bone marrow transplantation in children with hematological malignancies
Bone Marrow Transplantation, 1992
Acute intravascular haemolysis associated with high dose immunoglobulin after bone marrow transplantation for acute myelogenous leukemia
A. Rovelli, P. D'angelo, A. Balduzzi, P. Borzini, A. Biondi, et al.
Leukemia and Lymphoma, 1991
Overdose of vinblastine in a child with langerhans' cell histiocytosis: Toxicity and salvage therapy
V. Conter, M. L. Rabbone, M. Jankovic, D. Fraschini, A. Corbetta, et al.
Pediatric Hematology and Oncology, 1991
Thiamine responsive megaloblastic anemia: A ten-years therapy follow-up
Haematologica, 1989
Height of children off therapy after acute lymphoblastic leukemia
Maria Grazia Zurlo, Elisabetta Senesi, Benedetto Terracini, Donato Balducci, PierfranCo Biddau, et al.
Pediatric Hematology and Oncology, 1988

Paolo D'Angelo

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