Lista de obras - Raffaele Iorio - Dominio Público Uruguay

Aberrance of Serum Zinc and Free Copper Level in Wilson Disease

An adolescent with multinodular liver at ultrasound scanning

artículo científico publicado en 2000

Autoimmune hepatitis type 2 associated with an unexpected and transient presence of primary biliary cirrhosis-specific antimitochondrial antibodies: a case study and review of the literature.

artículo científico publicado en 2012

Characterization of liver involvement in defects of cholesterol biosynthesis: long-term follow-up and review

artículo científico publicado en 2005

Children with chronic hepatitis C: what future?

scientific article published on 01 August 2008

Cholestasis in neonatal intensive care unit: incidence, aetiology and management.

artículo científico publicado en 2009

Chronic hepatitis C in childhood: an 18-year experience.

artículo científico publicado en 2005

DNA and RNA studies for molecular characterization of a gross deletion detected in homozygosity in the NH2-terminal region of the ATP7B gene in a Wilson disease patient.

artículo científico publicado en 2011

Defective interleukin-2 production in children with chronic hepatitis B: role of adherent cells

artículo científico publicado en 1997

Diagnostic role of US for biliary atresia

scientific article published on 01 June 2008

Early occurrence of hypertransaminasemia in a 13-month-old child with Wilson disease

artículo científico publicado en 2003

Efficacy of combined antiviral therapy with lamivudine and tenofovir in a liver transplanted girl with de novo hepatitis B virus infection.

artículo científico publicado en 2013

Epidemiological profile of 806 Italian children with hepatitis C virus infection over a 15-year period

artículo científico publicado en 2007

Evolution of hepatitis C viral quasispecies and hepatic injury in perinatally infected children followed prospectively

artículo científico publicado en 2006

Expert opinion on current therapies for nonalcoholic fatty liver disease.

artículo científico publicado en 2011

False diagnosis of chronic non-A, non-B hepatitis hiding a case of glycogen storage disease

scientific article published on 01 June 1994

Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome.

artículo científico publicado en 2010

Gamma interferon release assays for diagnosis of tuberculosis infection in immune-compromised children in a country in which the prevalence of tuberculosis is low.

artículo científico publicado en 2009

Genotype-phenotype correlation in Italian children with Wilson's disease

artículo científico publicado en 2008

Health-related quality of life in pediatric liver transplanted patients compared with a chronic liver disease group

artículo científico publicado en 2013

Hepatic steatosis is uncommon in children with chronic hepatitis B

artículo científico publicado en 2009

Hyper-gamma-glutamyltransferase is commonly present in non-breast-fed infants with biliary atresia successfully treated with portoenterostomy

scientific article published on 01 July 2006

Hypertransaminasemia in childhood as a marker of genetic liver disorders.

artículo científico publicado en 2005

Immune phenotype and serum leptin in children with obesity-related liver disease

scientific article published on 25 October 2005

Impact of hepatitis B vaccination in a highly endemic area of south Italy and long-term duration of anti-HBs antibody in two cohorts of vaccinated individuals

artículo científico publicado en 2007

Is HCV infection associated with liver steatosis also in children?

article published in 2006

Is HCV infection associated with liver steatosis also in children?

artículo científico publicado en 2006

Is alpha-interferon treatment useful in children with non-B, non-C chronic hepatitis?

artículo científico publicado en 1995

Is exchange transfusion a possible treatment for neonatal hemochromatosis?

artículo científico publicado en 2007

Isolated liver transplantation in children with intestinal failure-associated liver disease: a still-debated matter

scientific article published on 01 March 2009

Leptin: the prototypic adipocytokine and its role in NAFLD.

scientific article published on June 2010

Long-term outcome in children with chronic hepatitis B: a 24-year observation period

artículo científico publicado en 2007

Low virological response to interferon in children with chronic hepatitis C.

artículo científico publicado en 1999

Management of autoimmune hepatitis in children: how many steps away from common agreement?

scientific article published on 01 October 2012

Management of cholelithiasis in Italian children: a national multicenter study

artículo científico publicado en 2008

Mass vaccination against hepatitis B in infants in Italy

scientific article published on 01 November 1988

Neonatal hemochromatosis and exchange transfusion: treating the disorder as an alloimmune disease

artículo científico publicado en 2010

Neutralizing antibodies to hepatitis C virus in perinatally infected children followed up prospectively

artículo científico publicado en 2011

Penicillamine-Related Neurologic Syndrome in a Child Affected by Wilson Disease With Hepatic Presentation ⬇️

artículo científico publicado el 1 de septiembre de 1997

Penicillamine-induced Elastosis Perforans Serpiginosa in Wilson Disease: Is Useful Switching to Zinc?

artículo científico publicado en 2017

Predictive value of Epstein-Barr virus genome copy number and BZLF1 expression in blood lymphocytes of transplant recipients at risk for lymphoproliferative disease.

artículo científico publicado en 2000

Prevalence and long-term course of macro-aspartate aminotransferase in children

artículo científico publicado en 2008

Randomised Clinical Trial: Calorie Restriction Regimen with Tomato Juice Supplementation Ameliorates Oxidative Stress and Preserves a Proper Immune Surveillance Modulating Mitochondrial Bioenergetics of T-Lymphocytes in Obese Children Affected by No

scientific article published on 04 January 2020

Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease

artículo científico publicado en 2010

Re: Possible prevention of fulminant hepatic failure in four children with acute severe hepatitis

artículo científico publicado en 2005

Severe Raynaud's phenomenon with chronic hepatis C disease treated with interferon

scientific article published on 01 February 2003

Side effects of alpha-interferon therapy and impact on health-related quality of life in children with chronic viral hepatitis ⬇️

artículo científico publicado el 1 de octubre de 1997

Steroid therapy for a case of severe drug-induced cholestasis

artículo científico publicado en 2006

Subclinical neurological involvement does not develop if Wilson's disease is treated early.

artículo científico publicado en 2016

Successful use of ursodeoxycholic acid in nodular regenerative hyperplasia of the liver

artículo científico publicado en 2011

The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease

artículo científico publicado en 2006

The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration

artículo científico publicado en 2017

Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin

artículo científico publicado en 2007

Ultrasound scanning in infants with biliary atresia: the different implications of biliary tract features and liver echostructure.

artículo científico publicado en 2013

What evidence exists to support antiviral treatment in children with chronic hepatitis B?

artículo científico publicado en 2013

Wilson disease: a matter of copper, but also of zinc

artículo científico publicado en 2015

Wilson disease: what is still unclear in pediatric patients?

artículo científico

Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene.

artículo científico publicado en 2015

Wilson's disease: Prospective developments towards new therapies.

artículo científico publicado en 2017

Zinc monotherapy is effective in Wilson's disease patients with mild liver disease diagnosed in childhood: a retrospective study

artículo científico publicado en 2014

Lista de obras de Raffaele Iorio

Aberrance of Serum Zinc and Free Copper Level in Wilson Disease

An adolescent with multinodular liver at ultrasound scanning

Autoimmune hepatitis type 2 associated with an unexpected and transient presence of primary biliary cirrhosis-specific antimitochondrial antibodies: a case study and review of the literature.

Characterization of liver involvement in defects of cholesterol biosynthesis: long-term follow-up and review

Children with chronic hepatitis C: what future?

Cholestasis in neonatal intensive care unit: incidence, aetiology and management.

Chronic hepatitis C in childhood: an 18-year experience.

DNA and RNA studies for molecular characterization of a gross deletion detected in homozygosity in the NH2-terminal region of the ATP7B gene in a Wilson disease patient.

Defective interleukin-2 production in children with chronic hepatitis B: role of adherent cells

Diagnostic role of US for biliary atresia

Early occurrence of hypertransaminasemia in a 13-month-old child with Wilson disease

Efficacy of combined antiviral therapy with lamivudine and tenofovir in a liver transplanted girl with de novo hepatitis B virus infection.

Epidemiological profile of 806 Italian children with hepatitis C virus infection over a 15-year period

Evolution of hepatitis C viral quasispecies and hepatic injury in perinatally infected children followed prospectively

Expert opinion on current therapies for nonalcoholic fatty liver disease.

False diagnosis of chronic non-A, non-B hepatitis hiding a case of glycogen storage disease

Fulminant hepatic failure requiring liver transplantation in 22q13.3 deletion syndrome.

Gamma interferon release assays for diagnosis of tuberculosis infection in immune-compromised children in a country in which the prevalence of tuberculosis is low.

Genotype-phenotype correlation in Italian children with Wilson's disease

Health-related quality of life in pediatric liver transplanted patients compared with a chronic liver disease group

Hepatic steatosis is uncommon in children with chronic hepatitis B

Hyper-gamma-glutamyltransferase is commonly present in non-breast-fed infants with biliary atresia successfully treated with portoenterostomy

Hypertransaminasemia in childhood as a marker of genetic liver disorders.

Immune phenotype and serum leptin in children with obesity-related liver disease

Impact of hepatitis B vaccination in a highly endemic area of south Italy and long-term duration of anti-HBs antibody in two cohorts of vaccinated individuals

Is HCV infection associated with liver steatosis also in children?

Is HCV infection associated with liver steatosis also in children?

Is alpha-interferon treatment useful in children with non-B, non-C chronic hepatitis?

Is exchange transfusion a possible treatment for neonatal hemochromatosis?

Isolated liver transplantation in children with intestinal failure-associated liver disease: a still-debated matter

Leptin: the prototypic adipocytokine and its role in NAFLD.

Long-term outcome in children with chronic hepatitis B: a 24-year observation period

Low virological response to interferon in children with chronic hepatitis C.

Management of autoimmune hepatitis in children: how many steps away from common agreement?

Management of cholelithiasis in Italian children: a national multicenter study

Mass vaccination against hepatitis B in infants in Italy

Neonatal hemochromatosis and exchange transfusion: treating the disorder as an alloimmune disease

Neutralizing antibodies to hepatitis C virus in perinatally infected children followed up prospectively

Penicillamine-Related Neurologic Syndrome in a Child Affected by Wilson Disease With Hepatic Presentation ⬇️

Penicillamine-induced Elastosis Perforans Serpiginosa in Wilson Disease: Is Useful Switching to Zinc?

Predictive value of Epstein-Barr virus genome copy number and BZLF1 expression in blood lymphocytes of transplant recipients at risk for lymphoproliferative disease.

Prevalence and long-term course of macro-aspartate aminotransferase in children

Randomised Clinical Trial: Calorie Restriction Regimen with Tomato Juice Supplementation Ameliorates Oxidative Stress and Preserves a Proper Immune Surveillance Modulating Mitochondrial Bioenergetics of T-Lymphocytes in Obese Children Affected by No

Re-evaluation of the diagnostic criteria for Wilson disease in children with mild liver disease

Re: Possible prevention of fulminant hepatic failure in four children with acute severe hepatitis

Severe Raynaud's phenomenon with chronic hepatis C disease treated with interferon

Side effects of alpha-interferon therapy and impact on health-related quality of life in children with chronic viral hepatitis ⬇️

Steroid therapy for a case of severe drug-induced cholestasis

Subclinical neurological involvement does not develop if Wilson's disease is treated early.

Successful use of ursodeoxycholic acid in nodular regenerative hyperplasia of the liver

The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease

The natural history of primary sclerosing cholangitis in 781 children: A multicenter, international collaboration

Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin

Ultrasound scanning in infants with biliary atresia: the different implications of biliary tract features and liver echostructure.

What evidence exists to support antiviral treatment in children with chronic hepatitis B?

Wilson disease: a matter of copper, but also of zinc

Wilson disease: what is still unclear in pediatric patients?

Wilson's disease caused by alternative splicing and Alu exonization due to a homozygous 3039-bp deletion spanning from intron 1 to exon 2 of the ATP7B gene.

Wilson's disease: Prospective developments towards new therapies.

Zinc monotherapy is effective in Wilson's disease patients with mild liver disease diagnosed in childhood: a retrospective study