P. Trombini

发表

Hereditary hyperferritinemia cataract syndrome: a de novo mutation in the iron responsive element of the L-ferritin gene.

C. Arosio, L. Fossati, M. Viganò, 1999, Haematologica.

Expression of hepcidin and other iron-related genes in type 3 hemochromatosis due to a novel mutation in transferrin receptor-2

D. Barisani, P. Trombini, A. Piperno, 2009, Haematologica.

A time course of hepcidin response to iron challenge in patients with HFE and TFR2 hemochromatosis

D. Girelli, T. Ganz, M. Sandri, 2011, Haematologica.

BLUNTED HEPCIDIN RESPONSE TO ORAL IRON CHALLENGE IN HFE-HEMOCHROMATOSIS

D. Girelli, T. Ganz, E. Nemeth, 2007 .

Blunted hepcidin response to oral iron challenge in HFE-related hemochromatosis.

D. Girelli, T. Ganz, E. Nemeth, 2007, Blood.

Iron Metabolism in Thalassemia and Sickle Cell Disease.

P. Trombini, A. Piperno, R. Mariani, 2009, Mediterranean journal of hematology and infectious diseases.

Hepcidin response to acute iron intake and chronic iron loading in dysmetabolic iron overload syndrome

T. Ganz, E. Nemeth, P. Trombini, 2011, Liver international : official journal of the International Association for the Study of the Liver.

Measurement of urinary hepcidin levels by SELDI-TOF-MS in HFE-hemochromatosis.

D. Girelli, O. Olivieri, T. Ganz, 2008, Blood cells, molecules & diseases.

Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia

T. Ganz, E. Nemeth, A. Biondi, 2007, Haematologica.

Insulin resistance influences iron metabolism and hepatic steatosis in type II diabetes

M. Viganò, P. Trombini, A. Piperno, 2000 .

Increased serum ferritin is common in men with essential hypertension

G. Mancia, P. Trombini, A. Piperno, 2002, Journal of hypertension.

Effects of venesections and restricted diet in patients with the insulin‐resistance hepatic iron overload syndrome

G. Mancia, G. Boari, M. Viganò, 2004, Liver international : official journal of the International Association for the Study of the Liver.

α1‐Antitrypsin mutations in NAFLD: High prevalence and association with altered iron metabolism but not with liver damage

R. Ceriani, S. Fargion, A. Fracanzani, 2006, Hepatology.

Genetic and metabolic factors are associated with increased hepatic iron stores in a selected population of p.Cys282Tyr heterozygotes.

C. Arosio, P. Trombini, A. Piperno, 2010, Blood cells, molecules & diseases.

S65c frequency in Italian patients with hemochromatosis, porphyria cutanea tarda and chronic viral hepatitis with iron overload.

C. Arosio, P. Trombini, A. Piperno, 2001, Haematologica.

Two novel nonsense mutations of HFE gene in five unrelated italian patients with hemochromatosis.

G. Mancia, C. Arosio, L. Fossati, 2000, Gastroenterology.

Prevalence of HFE mutations in upper Northern Italy: study of 1132 unrelated blood donors.

C. Arosio, C. Oberkanins, L. Fossati, 2003, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

Hepcidin modulation in human diseases: from research to clinic.

D. Girelli, P. Trombini, A. Piperno, 2009, World journal of gastroenterology.

Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron Overload.

D. Barisani, T. Ganz, S. Galimberti, 2008, Journal of hepatology.

Hepcidin Expression in Iron Overload Diseases Is Variably Modulated by Circulating Factors

D. Barisani, T. Ganz, P. Trombini, 2012, PloS one.

Revaluation of clinical and histological criteria for diagnosis of dysmetabolic iron overload syndrome.

R. Facchetti, G. Bovo, P. Trombini, 2008, World journal of gastroenterology.

Novel mutations of the ferroportin gene (SLC40A1): analysis of 56 consecutive patients with unexplained iron overload

P. Trombini, A. Piperno, S. Pelucchi, 2007, Clinical genetics.

Simultaneous liver iron and fat measures by magnetic resonance imaging in patients with hyperferritinemia

S. Galimberti, G. Bovo, I. Redaelli, 2015, Scandinavian journal of gastroenterology.

Ferritin, metabolic syndrome and NAFLD: elective attractions and dangerous liaisons.

P. Trombini, A. Piperno, 2007, Journal of hepatology.

Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation

M. Grisoli, A. Piga, C. Arosio, 2004, Gut.

CYBRD1 as a modifier gene that modulates iron phenotype in HFE p.C282Y homozygous patients

D. Girelli, C. Specchia, S. Calza, 2012, Haematologica.