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Journal of Pediatric Endocrinology & Metabolism : JPEM|October 11, 2001
Recombinant growth hormone treatment in short patients with thalassemia major: results after 24 and 36 monthsL Cavallo, A Acquafredda, C Zecchino, et al.
Immunopharmacology and Immunotoxicology|September 13, 2007
Modeling of granulocyte cytoskeletal responses following fMLP challengingM A Panaro, A Cianciulli, A Acquafredda, et al.
Immunopharmacology and Immunotoxicology|August 24, 2005
Structural similarities between mRNA for the formyl peptide receptors and 18S rRNAM A Panaro, A Acquafredda, M Sisto, et al.
Immunopharmacology and Immunotoxicology|September 13, 2007
Formyl peptide receptors on immune and nonimmune cells: analysis of sequence conservation in FPR genesM A Panaro, A Acquafredda, M Sisto, et al.
Journal of Endocrinological Investigation|June 22, 2005
Final height in short polytransfused thalassemia major patients treated with recombinant growth hormoneL Cavallo, V De Sanctis, M Cisternino, et al.
Comparative Immunology, Microbiology and Infectious Diseases|September 20, 2001
Inducible nitric oxide synthase expression in Leishmania-infected dog macrophagesM Sisto, O Brandonisio, M A Panaro, et al.
International Journal of Clinical & Laboratory Research|December 11, 1999
Inducible nitric oxide synthase and nitric oxide production in Leishmania infantum-infected human macrophages stimulated with interferon-gamma and bacterial lipopolysaccharideM A Panaro, A Acquafredda, S Lisi, et al.
Acta Endocrinologica|September 1, 1984
Endocrine involvement in children with beta-thalassaemia major. Transverse and longitudinal studies. I. Pituitary-thyroidal axis function and its correlation with serum ferritin levelsL Cavallo, D Licci, A Acquafredda, et al.
Journal of Autoimmunity|June 27, 2006
Autoantibodies from Sjögren's syndrome induce activation of both the intrinsic and extrinsic apoptotic pathways in human salivary gland cell line A-253M Sisto, S Lisi, D Castellana, et al.
The Journal of Clinical Endocrinology and Metabolism|August 17, 2006
Divergent phenotype of two siblings human leukocyte antigen identical, affected by nonclassical and classical congenital adrenal hyperplasia caused by 21-hydroxylase deficiencyO Porzio, V Cunsolo, M Malaponti, et al.
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