Lista de obras - Pier Luigi Calvo - Dominio Público Uruguay

An UPLC-MS/MS method coupled with automated on-line SPE for quantification of tacrolimus in peripheral blood mononuclear cells.

artículo científico publicado en 2015

An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia

artículo científico publicado en 2017

Attempt to Determine the Prevalence of Two Inborn Errors of Primary Bile Acid Synthesis: Results of a European Survey.

artículo científico publicado en 2017

Characterization of antimitochondrial antibodies in healthy adults ⬇️

artículo científico publicado el 1 de marzo de 1998

Clinical significance of the antibody to the putative core protein of hepatitis C virus in patients with chronic liver disease ⬇️

artículo científico publicado el 1 de agosto de 1993

Comparative analysis of rs12979860 SNP of the IFNL3 gene in children with hepatitis C and ethnic matched controls using 1000 Genomes Project data

artículo científico publicado en 2014

Donor CYP3A5 genotype influences tacrolimus disposition on the first day after paediatric liver transplantation.

artículo científico publicado en 2017

EBV induces HERV-K and HERV-W expression in pediatrics liver transplant recipients?

artículo científico publicado en 2015

EBV-encoded microRNAs profile evaluation in pediatric liver transplant recipients

artículo científico publicado en 2017

Early Liver Transplantation for Neonatal-Onset Methylmalonic Acidemia.

artículo científico publicado en 2015

Efficacy of intravenous immunoglobulin therapy in giant cell hepatitis with autoimmune hemolytic anemia: A multicenter study

artículo científico publicado en 2015

First UHPLC-MS/MS method coupled with automated online SPE for quantification both of tacrolimus and everolimus in peripheral blood mononuclear cells and its application on samples from co-treated pediatric patients

artículo científico publicado en 2017

Fontan circulation causes early, severe liver damage. Should we offer patients a tailored strategy?

artículo científico publicado en 2016

Hepatitis B virus unable to secrete e antigen and response to interferon in chronic hepatitis B.

artículo científico publicado en 1993

Hepatitis C virus heteroduplex tracking assay : application to genotype determination, quasispecies analysis, and molecular evolution studies.

artículo científico publicado en 1999

Hepatitis C virus infection and liver disease.

artículo científico publicado en 1995

Hepatitis C virus markers in patients with long-term biochemical and histological remission of chronic hepatitis.

artículo científico publicado en 1994

Interleukin 28B rs12979860 single-nucleotide polymorphism predicts spontaneous clearance of hepatitis C virus in children

artículo científico publicado en 2014

Isolated liver transplantation in an infant with ultrashort gut

scientific article published on 01 July 2006

Liver transplantation in defects of cholesterol biosynthesis: the case of lathosterolosis

artículo científico publicado en 2014

Liver transplantation in severe methylmalonic acidemia: The sooner, the better

scientific article published on 09 September 2015

Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx.

artículo científico publicado en 2008

Monitoring the natural course and response to therapy of chronic hepatitis B with an automated semi-quantitative assay for IgM anti-HBc

artículo científico publicado en 1993

NBAS mutations cause acute liver failure: when acetaminophen is not a culprit

artículo científico publicado en 2017

Neonatal chitotriosidase activity is not predictive for Niemann-Pick disease type A/B: implications for newborn screening for lysosomal storage disorders.

artículo científico publicado en 2012

Precore mutant hepatitis B virus and outcome of chronic infection and hepatitis in hepatitis B e antigen-positive children.

artículo científico publicado en 1994

Quantitative analysis of wild-type and HBeAg minus hepatitis B viruses by a sequence-dependent primer extension assay

scientific article published on 01 July 1994

Relations between hepatitis delta virus pathogenicity and hepatitis B virus heterogeneity.

artículo científico publicado en 1993

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation

scientific journal article

Thiopurine S-methyltransferase pharmacogenetics in a large-scale healthy Italian-Caucasian population: differences in enzyme activity.

artículo científico publicado en 2009

Transient elastography for non-invasive evaluation of post-transplant liver graft fibrosis in children.

artículo científico publicado en 2018

Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene.

artículo científico publicado en 2009

Lista de obras de Pier Luigi Calvo

An UPLC-MS/MS method coupled with automated on-line SPE for quantification of tacrolimus in peripheral blood mononuclear cells.

An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia

Attempt to Determine the Prevalence of Two Inborn Errors of Primary Bile Acid Synthesis: Results of a European Survey.

Characterization of antimitochondrial antibodies in healthy adults ⬇️

Clinical significance of the antibody to the putative core protein of hepatitis C virus in patients with chronic liver disease ⬇️

Comparative analysis of rs12979860 SNP of the IFNL3 gene in children with hepatitis C and ethnic matched controls using 1000 Genomes Project data

Donor CYP3A5 genotype influences tacrolimus disposition on the first day after paediatric liver transplantation.

EBV induces HERV-K and HERV-W expression in pediatrics liver transplant recipients?

EBV-encoded microRNAs profile evaluation in pediatric liver transplant recipients

Early Liver Transplantation for Neonatal-Onset Methylmalonic Acidemia.

Efficacy of intravenous immunoglobulin therapy in giant cell hepatitis with autoimmune hemolytic anemia: A multicenter study

First UHPLC-MS/MS method coupled with automated online SPE for quantification both of tacrolimus and everolimus in peripheral blood mononuclear cells and its application on samples from co-treated pediatric patients

Fontan circulation causes early, severe liver damage. Should we offer patients a tailored strategy?

Hepatitis B virus unable to secrete e antigen and response to interferon in chronic hepatitis B.

Hepatitis C virus heteroduplex tracking assay : application to genotype determination, quasispecies analysis, and molecular evolution studies.

Hepatitis C virus infection and liver disease.

Hepatitis C virus markers in patients with long-term biochemical and histological remission of chronic hepatitis.

Interleukin 28B rs12979860 single-nucleotide polymorphism predicts spontaneous clearance of hepatitis C virus in children

Isolated liver transplantation in an infant with ultrashort gut

Liver transplantation in defects of cholesterol biosynthesis: the case of lathosterolosis

Liver transplantation in severe methylmalonic acidemia: The sooner, the better

Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx.

Monitoring the natural course and response to therapy of chronic hepatitis B with an automated semi-quantitative assay for IgM anti-HBc

NBAS mutations cause acute liver failure: when acetaminophen is not a culprit

Neonatal chitotriosidase activity is not predictive for Niemann-Pick disease type A/B: implications for newborn screening for lysosomal storage disorders.

Precore mutant hepatitis B virus and outcome of chronic infection and hepatitis in hepatitis B e antigen-positive children.

Quantitative analysis of wild-type and HBeAg minus hepatitis B viruses by a sequence-dependent primer extension assay

Relations between hepatitis delta virus pathogenicity and hepatitis B virus heterogeneity.

TMEM199 Deficiency Is a Disorder of Golgi Homeostasis Characterized by Elevated Aminotransferases, Alkaline Phosphatase, and Cholesterol and Abnormal Glycosylation

Thiopurine S-methyltransferase pharmacogenetics in a large-scale healthy Italian-Caucasian population: differences in enzyme activity.

Transient elastography for non-invasive evaluation of post-transplant liver graft fibrosis in children.

Variable phenotypic expression of chylomicron retention disease in a kindred carrying a mutation of the Sara2 gene.