List of works - Alberto Piperno

Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association

scientific article published on December 1, 1992

Heterogeneity of hemochromatosis in Italy

scientific article published on 01 May 1998

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.

scientific article

Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis

scientific article

Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis

scientific article published on 01 April 1992

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

article

Modulation of hepcidin production during hypoxia-induced erythropoiesis in humans in vivo: data from the HIGHCARE project

scientific article

High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

article

Hepatic iron overload in patients with chronic viral hepatitis: role of HFE gene mutations.

scientific article published in October 1998

Increased serum ferritin is common in men with essential hypertension

scientific article published on 01 August 2002

Time course of circulatory and humoral effects of rapid total paracentesis in cirrhotic patients with tense, refractory ascites.

scientific article

The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis.

scientific article

Hepcidin modulation in human diseases: from research to clinic.

scientific article published on February 2009

Early impairment of large artery structure and function in type I diabetes mellitus

scientific article published on 01 August 1999

HCV genotypes in Northern Italy: a survey of 1368 histologically proven chronic hepatitis C patients.

scientific article published on November 1998

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

article

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

scientific article published on 01 August 2000

Prognostic factors for hepatocellular carcinoma in genetic hemochromatosis

scientific article published on 01 December 1994

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

scientific article published on May 2004

Cardiac alterations in 36 consecutive patients with idiopathic haemochromatosis: polygraphic and echocardiographic evaluation.

scientific article

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

scientific article

A phase 1/2, dose-escalation trial of deferasirox for the treatment of iron overload in HFE-related hereditary hemochromatosis

scientific article

Changes in 24 h ambulatory blood pressure and effects of angiotensin II receptor blockade during acute and prolonged high-altitude exposure: a randomized clinical trial

Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F

scientific article

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

scientific article published on 6 July 2012

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

scientific article published on August 2008

Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia

article

Serum type III procollagen peptide in alcoholic liver disease and idiopathic hemochromatosis: its relationship to hepatic fibrosis, activity of the disease and iron overload

scientific article published on 01 May 1985

Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)

scientific article (publication date: 15 March 2004)

Haemochromatosis in patients with beta-thalassaemia trait

scientific article published on 01 December 2000

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

scientific article

The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients

scientific article published on 01 July 1996

Genetic hemochromatosis in Italian patients with prophyria cutanea tarda: possible explanation for iron overload

article

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders

scientific article published on 09 June 2010

Inherited HFE-unrelated hemochromatosis in Italian families

article

Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis

scientific article published on 18 October 2014

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome

scientific article published on 01 November 2001

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

scientific article published on 26 January 2007

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

scientific article published on 27 December 2007

Index measured at an intermediate altitude to predict impending acute mountain sickness

scientific article published on 01 October 2011

Association of hereditary spherocytosis and idiopathic hemochromatosis. A synergistic effect in determining iron overload.

scientific article published in November 1986

Circulating factors are involved in hypoxia-induced hepcidin suppression.

scientific article

Effects of hematocrit changes on flow-mediated and metabolic vasodilation in humans

scientific article published on 01 July 2002

Low-dose interleukin-2 subcutaneous immunotherapy in association with the pineal hormone melatonin as a first-line therapy in locally advanced or metastatic hepatocellular carcinoma

scientific article published on 01 January 1994

Preclinical hypogonadism in genetic hemochromatosis in the early stage of the disease: evidence of hypothalamic dysfunction

scientific article published on June 1, 1992

Modulation of urinary peptidome in humans exposed to high altitude hypoxia

Hepcidin expression in iron overload diseases is variably modulated by circulating factors

scientific article

Molecular diagnosis of hemochromatosis.

scientific article

Radial artery wall alterations in genetic hemochromatosis before and after iron depletion therapy

scientific article published on 01 September 2000

Iron overload in subjects with beta-thalassaemia trait: role of idiopathic haemochromatosis gene

scientific article published on 01 November 1985

List of works by Alberto Piperno

Hepatitis C virus and porphyria cutanea tarda: evidence of a strong association

Heterogeneity of hemochromatosis in Italy

New mutations inactivating transferrin receptor 2 in hemochromatosis type 3.

Spectrum of hemojuvelin gene mutations in 1q-linked juvenile hemochromatosis

Survival and prognostic factors in 212 Italian patients with genetic hemochromatosis

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

Modulation of hepcidin production during hypoxia-induced erythropoiesis in humans in vivo: data from the HIGHCARE project

High prevalence of the His63Asp HFE mutation in italian patients with porphyria cutanea tarda

Hepatic iron overload in patients with chronic viral hepatitis: role of HFE gene mutations.

Increased serum ferritin is common in men with essential hypertension

Time course of circulatory and humoral effects of rapid total paracentesis in cirrhotic patients with tense, refractory ascites.

The mitochondrial superoxide dismutase A16V polymorphism in the cardiomyopathy associated with hereditary haemochromatosis.

Hepcidin modulation in human diseases: from research to clinic.

Early impairment of large artery structure and function in type I diabetes mellitus

HCV genotypes in Northern Italy: a survey of 1368 histologically proven chronic hepatitis C patients.

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

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

Prognostic factors for hepatocellular carcinoma in genetic hemochromatosis

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

Cardiac alterations in 36 consecutive patients with idiopathic haemochromatosis: polygraphic and echocardiographic evaluation.

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

A phase 1/2, dose-escalation trial of deferasirox for the treatment of iron overload in HFE-related hereditary hemochromatosis

Changes in 24 h ambulatory blood pressure and effects of angiotensin II receptor blockade during acute and prolonged high-altitude exposure: a randomized clinical trial

Linkage analysis of 6p21 polymorphic markers and the hereditary hemochromatosis: localization of the gene centromeric to HLA-F

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

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

Effects of plasma transfusion on hepcidin production in human congenital hypotransferrinemia

Serum type III procollagen peptide in alcoholic liver disease and idiopathic hemochromatosis: its relationship to hepatic fibrosis, activity of the disease and iron overload

Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)

Haemochromatosis in patients with beta-thalassaemia trait

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

The ancestral hemochromatosis haplotype is associated with a severe phenotype expression in Italian patients

Genetic hemochromatosis in Italian patients with prophyria cutanea tarda: possible explanation for iron overload

Measurement of serum hepcidin-25 levels as a potential test for diagnosing hemochromatosis and related disorders

Inherited HFE-unrelated hemochromatosis in Italian families

Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis

Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome

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

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

Index measured at an intermediate altitude to predict impending acute mountain sickness

Association of hereditary spherocytosis and idiopathic hemochromatosis. A synergistic effect in determining iron overload.

Circulating factors are involved in hypoxia-induced hepcidin suppression.

Effects of hematocrit changes on flow-mediated and metabolic vasodilation in humans

Low-dose interleukin-2 subcutaneous immunotherapy in association with the pineal hormone melatonin as a first-line therapy in locally advanced or metastatic hepatocellular carcinoma

Preclinical hypogonadism in genetic hemochromatosis in the early stage of the disease: evidence of hypothalamic dysfunction

Modulation of urinary peptidome in humans exposed to high altitude hypoxia

Hepcidin expression in iron overload diseases is variably modulated by circulating factors

Molecular diagnosis of hemochromatosis.

Radial artery wall alterations in genetic hemochromatosis before and after iron depletion therapy

Iron overload in subjects with beta-thalassaemia trait: role of idiopathic haemochromatosis gene