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Autor:
Federico Nalesso, Matteo Rigato, Irene Cirella, Maria Paola Protti, Ruggero Zanella, Bartolomeo Rossi, Maria Caterina Putti, Francesca K. Martino, Lorenzo A. Calò
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 22; Pages: 6752
Beta-thalassemia syndromes are the most common inherited monogenic disorders worldwide. The most common pathophysiologic and clinical renal disease manifestations of in β-TM patients is the tubular dysfunctions related to iron overload, chronic anem