P. Samperi

发表

Lessons learned from the H1N1 pandemic: the need to improve systematic vaccination in Sickle Cell Disease children. A multi center survey in Italy.

S. Perrotta, L. Notarangelo, L. Sainati, 2011, Vaccine.

Second-line therapy in paediatric warm autoimmune haemolytic anaemia. Guidelines from the Associazione Italiana Onco-Ematologia Pediatrica (AIEOP).

S. Perrotta, A. Zanella, P. Giordano, 2018, Blood transfusion = Trasfusione del sangue.

HbS/β+ thalassemia: Really a mild disease? A National survey from the AIEOP Sickle Cell Disease Study Group with genotype‐phenotype correlation

S. Perrotta, P. Gorello, P. Giordano, 2019, European journal of haematology.

Triptorelin for Fertility Preservation in Adolescents Treated With Chemotherapy for Cancer

F. Bellia, S. Marino, A. Di Cataldo, 2018, Journal of pediatric hematology/oncology.

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

S. Perrotta, A. Zanella, L. Notarangelo, 2017, Blood transfusion = Trasfusione del sangue.

New Insights into Iron Deficiency Anemia in Children: A Practical Review

A. Di Cataldo, M. La Spina, G. Russo, 2022, Metabolites.

Evidence for the molecular heterogeneity of sickle cell anemia chromosomes bearing the βS/Benin haplotype

G. Patrinos, P. Kollia, G. Schilirò, 2005, American journal of hematology.

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

S. Perrotta, L. Sainati, R. Colombatti, 2013, Orphanet Journal of Rare Diseases.

Successful Treatment of a Very Late Isolated Relapse in an Adolescent With a PICALM-MLLT10 Positive T-lineage Acute Lymphoblastic Leukemia.

S. Marino, A. Di Cataldo, L. Lo Nigro, 2017, Journal of pediatric hematology/oncology.

Monitoring oral iron therapy in children with iron deficiency anemia: an observational, prospective, multicenter study of AIEOP patients (Associazione Italiana Emato-Oncologia Pediatrica)

P. Giordano, F. Giona, L. Notarangelo, 2020, Annals of Hematology.

Bronchial Hyperreactivity in Children With Sickle Cell Thalassemia

A. Barbato, G. Schilirò, M. Rosa, 1997 .

Genetic heterogeneity of beta-thalassemia in southeast Sicily.

T. Huisman, G. Schilirò, P. Samperi, 1995, American journal of hematology.

Acute events in children with sickle cell disease in Italy during the COVID‐19 pandemic: useful lessons learned

S. Perrotta, P. Giordano, F. Giona, 2021, British Journal of Haematology.

Diabetes insipidus 9 years after cessation of therapy for acute lymphoblastic leukemia.

A. Di Cataldo, P. Samperi, M. Caruso-Nicoletti, 1991, Pediatric hematology and oncology.

Treatment of visceral leishmaniasis with meglumine and allopurinol.

G. Schilirò, A. Di Cataldo, P. Samperi, 1993, American journal of diseases of children.

Dissection of the association status of two polymorphisms in the β‐globin gene cluster with variations in F‐cell number in non‐anemic individuals

D. Labie, J. Elion, T. Merghoub, 1997, American journal of hematology.

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals.

D. Labie, J. Elion, T. Merghoub, 1996, Blood.

Clinical, hematological, and molecular features in sicilians with Hb S‐β‐thalassemia

Rajesh K. Gupta, G. Schilirò, R. Testa, 1992 .

Iron status in white sickle cell disease patients

G. Schilirò, P. Samperi, G. Russo‐Mancuso, 1992, European journal of haematology.

Hydroxyurea prescription, availability and use for children with sickle cell disease in Italy: Results of a National Multicenter survey

S. Perrotta, L. Notarangelo, G. Forni, 2018, Pediatric blood & cancer.

Phenotype–genotype correlation in Sicilian patients with Hb H

G. Schilirò, A. Di Cataldo, M. La Spina, 2000, European journal of haematology.

Genetic heterogeneity of β‐thalassemia in southeast sicily

T. Huisman, G. Schilirò, P. Samperi, 1995 .

Clinical, hematological, and molecular features in Sicilians with sickle cell disease.

G. Schilirò, L. Lo Nigro, R. Testa, 1992, Hemoglobin.

High performance liquid chromatography (HPLC): a simple method to quantify Hb C, O-Arab, Agenogi and F.

G. Schilirò, A. Di Cataldo, P. Samperi, 2008, Clinical and laboratory haematology.

Six rare hemoglobin variants found in Sicily.

A. Di Cataldo, R. Testa, P. Samperi, 1991, Hemoglobin.

A mild form of Hb S‐β‐thalassemia syndrome is assured in Sicilian patients by β+mutant IVS‐I nt 6(T→C)

R. Testa, P. Samperi, V. Romano, 1997 .

Craniofacial morphology in patients with sickle cell disease: a cephalometric analysis.

G. Bertuna, P. Samperi, V. Licciardello, 2007, European journal of orthodontics.

Hematological findings in 375 Sicilians with Hb S trait.

G. Schilirò, R. Testa, P. Samperi, 1990, Haematologica.

General anesthesia, conscious sedation, or nothing: Decision‐making by children during painful procedures

M. Barchitta, A. Agodi, G. Parisi, 2019, Pediatric blood & cancer.

Liver involvement in white patients with sickle-cell disease.

G. Schilirò, P. Samperi, D. Di Bella, 1996, Archives of pediatrics & adolescent medicine.

Molecular Pathways in Childhood Acute Lymphoblastic Leukemia: From the Bench to the Bedside

A. Di Cataldo, L. Lo Nigro, P. Bonaccorso, 2015, Journal of Pediatric Biochemistry.

Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: effect of deferoxamine.

C. Di Giacomo, V. Sorrenti, A. Campisi, 1991, Pharmacological research.

Letter to the editor: Hemoglobin C disorders in whites

J. Opitz, G. Schilirò, M. Romeo, 1986 .

Hemoglobin C disorders in whites.

G. Schilirò, M. Romeo, P. Samperi, 1986, American journal of medical genetics.

Hb Agenogi [beta 90(F6)Glu----Lys] and beta zero-thalassemia in a Sicilian family.

G. Schilirò, P. Samperi, S. Dibenedetto, 1990, Hemoglobin.

Sensorineural hearing loss in sickle cell disease patients in Sicily.

G. Bertuna, P. Samperi, G. Poli, 2005, Minerva pediatrica.