RAVASI, GIULIA

RAVASI, GIULIA  

DIPARTIMENTO DI MEDICINA E CHIRURGIA (SCHOOL OF MEDICINE AND SURGERY)  

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Risultati 1 - 20 di 22 (tempo di esecuzione: 0.015 secondi).
Titolo Tipologia Data di pubblicazione Autori File
Modulation of hepcidin production during hypoxia-induced erythropoiesis in humans in vivo: data from the HIGHCARE project 01 - Articolo su rivista 2011 PIPERNO, ALBERTOGALIMBERTI, STEFANIAPELUCCHI, SARARAVASI, GIULIALOMBARDI, CAROLINABILO, GRZEGORZREVERA, MIRIAMGIULIANO, ANDREAFAINI, ANDREAMAININI, VERONICAVALSECCHI, MARIA GRAZIAMANCIA, GIUSEPPEPARATI, GIANFRANCO +
Hepcidin expression in iron overload diseases is variably modulated by circulating factors 01 - Articolo su rivista 2012 RAVASI, GIULIAPELUCCHI, SARATROMBINI, PAOLAMARIANI, RAFFAELLAPOZZI, MARCOBARISANI, DONATELLAPIPERNO, ALBERTO +
IRON AND HYPOXIA LINK: DOWNREGULATION OF LUCIFERASE ACTIVITY OF HEPCIDIN PROMOTER BY HYPOXIC SERA IN HUH-7 CELLS 02 - Intervento a convegno 2013 GRENI, FEDERICORAVASI, GIULIAPELUCCHI, SARABARISANI, DONATELLAPIPERNO, ALBERTO +
UNEXPLAINED ISOLATED HYPERFERRITINEMIA IN PATIENTS WITHOUT MUTATIONS IN FERRITIN GENE AND L-FERRITIN IRES REGIONS 02 - Intervento a convegno 2013 RAVASI, GIULIAPELUCCHI, SARATROMBINI, PAOLAMARIANI, RAFFAELLAGRENI, FEDERICOPIPERNO, ALBERTO +
Hypoxia-dependent hepcidin down-regulation: an in vitro study 02 - Intervento a convegno 2014 Ravasi,GGreni, FParati, GPelucchi, SPiperno, A +
Circulating factors are involved in hypoxia-induced hepcidin suppression 01 - Articolo su rivista 2014 RAVASI, GIULIAPELUCCHI, SARAGRENI, FEDERICOGIULIANO, ANDREAPARATI, GIANFRANCOPIPERNO, ALBERTO +
Transferrin receptor 2 mutations in patients with juvenile hemochromatosis phenotype 01 - Articolo su rivista 2015 RAVASI, GIULIARAUSA, MARCOPELUCCHI, SARAGRENI, FEDERICOMARIANI, RAFFAELLAPIPERNO, ALBERTO +
GNPAT rs11558492 is not associated to iron overload in Italian HFE p.C282Y homozygotes 02 - Intervento a convegno 2016 GRENI, FEDERICOMARIANI, RAFFAELLARAVASI, GIULIAPIPERNO, ALBERTOPELUCCHI, SARA +
Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis 01 - Articolo su rivista 2016 Pelucchi, SGalimberti, SGreni, FMariani, RRavasi, GValsecchi, MPiperno, A +
Hepcidin regulation in a mouse model of acute hypoxia 02 - Intervento a convegno 2016 RAVASI, GIULIAPELUCCHI, SARABUOLI COMANI, GAIAGRENI, FEDERICOMARIANI, RAFFAELLARIVOLTA, ILARIABARISANI, DONATELLAPIPERNO, ALBERTO +
Hypoxia-Dependent Hepcidin Down-Regulation: In Vitro and In Vivo Studies 07 - Tesi di dottorato Bicocca post 2009 2016 RAVASI, GIULIA
GNPAT rs11558492 is not a major modifier of iron status: Study of Italian hemochromatosis patients and blood donors 01 - Articolo su rivista 2017 GRENI, FEDERICOMARIANI, RAFFAELLARAVASI, GIULIAGALIMBERTI, STEFANIAPIPERNO, ALBERTOPELUCCHI, SARA +
Unexplained isolated hyperferritinemia without iron overload 01 - Articolo su rivista 2017 RAVASI, GIULIAPELUCCHI, SARAMARIANI, RAFFAELLAGRENI, FEDERICOPIPERNO, ALBERTO +
Hepcidin regulation in a mouse model of acute hypoxia 01 - Articolo su rivista 2018 Ravasi, GiuliaPelucchi, SaraBuoli Comani, GaiaGreni, FedericoMariani, RaffaellaBombelli, SilviaPerego, RobertoBarisani, DonatellaPiperno, Alberto +
A severe hemojuvelin mutation leading to late onset of HFE2-hemochromatosis 01 - Articolo su rivista 2018 Ravasi, GiuliaPelucchi, SaraMariani, RaffaellaPiperno, Alberto +
Phenotypic heterogeneity in seven Italian cases of aceruloplasminemia 01 - Articolo su rivista 2018 Pelucchi, SaraMariani, RaffaellaRavasi, GiuliaTremolizzo, LucioPiperno, Alberto +
Ferroportin disease: A novel SLC40A1 mutation 01 - Articolo su rivista 2020 Ravasi G.Pelucchi S.Piperno A. +
Ceruloplasmin variants might have different effects in different iron overload disorders 01 - Articolo su rivista 2021 Pelucchi, SaraRavasi, GiuliaPiperno, Alberto
Mental well-being in patients with transfusion-dependent anemias and hemochromatosis during the SARS-CoV-2 pandemic 01 - Articolo su rivista 2021 Ravasi G.Piperno A. +
Atypical phenotype in a patient with ceruloplasmin mutations in the compound heterozygous state 01 - Articolo su rivista 2021 Ravasi G.Pelucchi S.Piperno A. +