Search Results - "Busti, F"

CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients by PELUCCHI, Sara, MARIANI, Raffaella, GIRELLI, Domenico, FARGION, Silvia, SPECCHIA, Claudia, PIPERNO, Alberto, CALZA, Stefano, LUDOVICA FRACANZANI, Anna, LITTA MODIGNANI, Giulia, BERTOLA, Francesca, BUSTI, Fabiana, TROMBINI, Paola, FRAQUELLI, Mirella, LUCA FORNI, Gian

“…Most patients with hereditary hemochromatosis in the Caucasian population are homozygous for the p.C282Y mutation in the HFE gene. The penetrance and…”
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1133 A TIME COURSE OF HEPCIDIN RESPONSE TO ORAL IRON CHALLENGE IN HFE AND TFR2 HEMOCHROMATOSIS PATIENTS by Trombini, P, Busti, F, Campostrini, N, Sandri, M, Pelucchi, S, Nemeth, E, Ganz, T, Camaschella, C, Girelli, D, Piperno, A

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1 TIME COURSE OF HEPCIDIN RESPONSE TO ORAL IRON TEST CLARIFIES THE ROLE OF HFE AND TFR2 IN IRON SENSING by Trombini, P, Busti, F, Campostrini, N, Sandri, M, Pelucchi, S, Nemeth, E, Ganz, T, Camaschella, C, Girelli, D, Piperno, A

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Modern iron replacement therapy: clinical and pathophysiological insights by Girelli, Domenico, Ugolini, Sara, Busti, Fabiana, Marchi, Giacomo, Castagna, Annalisa

“…Iron deficiency, with or without anemia, is extremely frequent worldwide, representing a major public health problem. Iron replacement therapy dates back to…”
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Molecular characterization of patients with and without coronary artery disease with “extreme LDL-C phenotypes” by Brucato, F., Martinelli, N., Spina, R., Busti, F., Ingrassia, V., Scrimali, C., Altieri, G.I., Noto, D., Misiano, G., Giammanco, A., Barbagallo, C.M., Fayer, F., Cefalù, A.B., Olivieri, O., Girelli, D., Averna, M.

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A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis by GIRELLI, Domenico, TROMBINI, Paola, CAMASCHELLA, Clara, BUSTI, Fabiana, CAMPOSTRINI, Natascia, SANDRI, Marco, PELUCCHI, Sara, WESTERMAN, Mark, GANZ, Tomas, NEMETH, Elizabeta, PIPERNO, Alberto

“…Inadequate hepcidin production leads to iron overload in nearly all types of hemochromatosis. We explored the acute response of hepcidin to iron challenge in…”
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A PROPOSAL OF AN ALGORITHM FOR THE DIAGNOSIS OF TYPE 1 GAUCHER DISEASE STARTING FROM HYPERFERRITINEMIA IN ADULTS: PF502 by Marchi, G., Busti, F., Zidanes, Lira A., Castagna, A., Girelli, D.

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PS1294 MULTIFACTORIAL HEPCIDIN SUPPRESSION IN BETA‐THALASSEMIA CARRIERS WITH IRON OVERLOAD by Busti, F., Marchi, G., Castagna, A., Zidanes, A. Lira, Nemeth, E., Ganz, T., Girelli, D.

“…Background: Beta‐thalassemia carriers (βTc) can develop iron overload (IO), although infrequently. Traditional risk factors (alcohol abuse or liver diseases)…”
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PF502 A PROPOSAL OF AN ALGORITHM FOR THE DIAGNOSIS OF TYPE 1 GAUCHER DISEASE STARTING FROM HYPERFERRITINEMIA IN ADULTS by Marchi, G., Busti, F., Lira Zidanes, A., Castagna, A., Girelli, D.

“…Background: Type 1 Gaucher disease (GD) is a pleiotropic disease due to biallelic mutations in GBA gene, causing a reduction or absence of the activity of…”
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