Hydroxyurea

Milioni di anni Neuroblastoma: il prezzo della cura e le nuove frontiere Raro ma possibile Trent’anni di idrossiurea per l’anemia falciforme Curare la mamma cambia il cervello… della figlia Il ciclo della vita Indimenticabili

2025/9 — pag. 555-556 — DOI

Facciamo il punto sull’anemia falciforme

Tessitore A, Cuzzubbo D, Russo G.

2025/5 — pag. 296-298 — DOI

Sickle cell disease (SCD) is an increasingly relevant condition in Italy due to rising immigration from high-prevalence regions. Early diagnosis through newborn screening and comprehensive management - including hydroxyurea, antibiotic prophylaxis, t...

Drepanocitosi e osteonecrosi avascolare della testa del femore

Perfetto F, Pasquali E, Biserna L, Iacono A, Farneti C, Radice C, Marchetti F

2025/5 — pag. 123-124 — DOI

A 10.5-year-old girl with homozygous sickle cell disease on chronic treatment with hydroxyurea, blood transfusions and erythroexchange presented with sudden right thigh pain and limping, without trauma or fever. Imaging and lab results indicated avas...

Lesioni ossee simmetriche e drepanocitosi

Franzone D, Chianucci B, Basso L, Guardo D, Bellini T, Piccotti E.

2023/6 — pag. 399-402 — DOI

An 8-year-old boy suffering from sickle cell disease (SCD) was admitted to emergency unit complaining of moderate-to-severe pain in his lower limbs. He received chronic transfusion therapy and hydroxyurea. Apparently, he had never experienced vaso-oc...

Lesioni ossee simmetriche e drepanocitosi

Franzone D, Chianucci B, Basso L, Guardo D, Bellini T, Piccotti E

2023/6 — pag. 100-101 — DOI

An 8-year-old boy suffering from sickle cell disease (SCD) was admitted to emergency unit complaining of moderate-to-severe pain in his lower limbs. He received chronic transfusion therapy and hydroxyurea. Apparently, he had never experienced vaso-oc...

Anemia falciforme e sindrome toracica acuta

G. Graziani, J. Gencarelli, C. Lama, S. Brocchi, L. Biserna, C. Radice, F. Marchetti

2020/6 — pag. 392-394

Anemia falciforme e sindrome toracica acuta

G. Graziani, J. Gencarelli, C. Lama, S. Brocchi, L. Biserna, C. Radice, F. Marchetti

2020/6 — pag. 126-129 — DOI

La gestione condivisa ospedale-territorio del bambino con malattia drepanocitica

P. Samperi, R. Colombatti, E. Cannata, L. Sainati, G. Russo

2017/10 — pag. 629-635

Sickle cell disease is a hereditary autosomal disease of haemoglobin characterized by chronic haemolytic anaemia, vaso-occlusive painful crisis, organ damage and increased susceptibility to infections. In recent years, the number of patients with s...

Il pediatra e lo specialista (e 25 anni di Confronti in Pediatria) Vitamina D: e uno Vitamina D: e due Vitamina D: e tre Cara, vecchia PCR Evidenze in medicina: il caso delle verruche plantari Anemia falciforme: idrossiurea da subito! Trattamento antibiotico breve per la meningite

2011/6 — pag. 353-354

L'anemia falciforme

M. Lazzerini, M. Rabusin

2006/4 — pag. 223-234

Sickle cell disease (SCD) is one of the most prevalent haemoglobinopathies in the world, being related to areas where malaria is or was endemic. In Italy the majority of patients still live in Sicily, where the overall HbS gene frequency is 2%. Domes...

Una dattilite bilaterale simmetrica

M. Lazzerini

2004/2