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Annals of Surgery|January 2, 2007
Asymptomatic cholelithiasis in children with sickle cell disease: early or delayed cholecystectomy?Giuseppe Currò, Anna Meo, Daniela Ippolito, et al.Chinese Clinical Oncology|September 13, 2022
The challenging surgical management of hepatic epithelioid hemangioendothelioma: a narrative reviewFrancesco Giovanardi, Zoe Larghi Laureiro, Gerardina Anna Meo, et al.European Journal of Haematology|May 7, 2005
Long-term treatment with deferiprone in a L1 veteranAnna Meo, Annalisa Ruggeri, Maria Angela La Rosa, et al.Hemoglobin|March 17, 2006
Iron burden and liver fibrosis decrease during a long-term phlebotomy program and iron chelating treatment after bone marrow transplantationAnna Meo, Annalisa Ruggeri, Maria A La Rosa, et al.Genetic Testing|December 4, 2003
Validation of dHPLC for molecular diagnosis of beta-thalassemia in Southern ItalyAlessia Colosimo, Valentina Guida, Anna Scolari, et al.Hemoglobin|August 12, 2003
Role of polymorphic sequences 5' to the G(gamma) gene and 5' to the beta gene on the homozygous beta thalassemic phenotypeMara Ferrara, Sofia M R Matarese, Matteo Francese, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|April 8, 2004
Osteoprotegerin and RANKL in the pathogenesis of thalassemia-induced osteoporosis: new pieces of the puzzleNunziata Morabito, Agostino Gaudio, Antonino Lasco, et al.Clinical Biochemistry|May 7, 2010
Role of genetic pattern on bone mineral density in thalassemic patientsAgostino Gaudio, Nancy Morabito, Anastasia Xourafa, et al.Haematologica|September 12, 2006
Risk factors for death in patients with beta-thalassemia major: results of a case-control studyAdriana Ceci, Paola Baiardi, Mariana Catapano, et al.Haematologica|October 13, 2004
Clinical and histological characterization of liver disease in patients with transfusion-dependent beta-thalassemia. A multicenter study of 117 casesDaniele Prati, Marco Maggioni, Silvano Milani, et al.Pageof 2