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Alberto Piperno

Showing results (41-50 of 91) with videos related to

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Blood|November 25, 2003
Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)Antonella Roetto, Filomena Daraio, Paolo Porporato, et al.
American Journal of Human Genetics|July 25, 2023
A form of inherited hyperferritinemia associated with bi-allelic pathogenic variants of STAB1Edoardo Monfrini, Sara Pelucchi, Maija Hollmén, et al.
World Journal of Gastroenterology|June 22, 2012
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosisLuca Valenti, Paolo Maggioni, Alberto Piperno, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|March 13, 2021
Prolonged exposure to welding fumes as a novel cause of systemic iron overloadRaffaella Mariani, Sara Pelucchi, Valentina Paolini, et al.
Haematologica|March 26, 2003
Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestryAlessandra Salvioni, Raffaella Mariani, Christian Oberkanins, et al.
Journal of Hepatology|May 9, 2008
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron OverloadDonatella Barisani, Sara Pelucchi, Raffaella Mariani, et al.
Alzheimer Disease and Associated Disorders|September 5, 2009
Higher than expected progranulin mutation rate in a case series of Italian FTLD patientsLucio Tremolizzo, Giorgio Gelosa, Alessio Galbussera, et al.
American Journal of Hematology|February 8, 2020
Hyperferritinemia and diagnosis of type 1 Gaucher diseaseGiacomo Marchi, Fabio Nascimbeni, Irene Motta, et al.
EMBO Molecular Medicine|November 30, 2017
Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemiaAlan Zanardi, Antonio Conti, Marco Cremonesi, et al.
European Journal of Haematology|March 16, 2018
Hepcidin regulation in a mouse model of acute hypoxiaGiulia Ravasi, Sara Pelucchi, Gaia Buoli Comani, et al.
Pageof 10

Showing results (41-50 of 91) with videos related to

Sort By:
Pageof 10
Blood|November 25, 2003
Screening hepcidin for mutations in juvenile hemochromatosis: identification of a new mutation (C70R)Antonella Roetto, Filomena Daraio, Paolo Porporato, et al.
American Journal of Human Genetics|July 25, 2023
A form of inherited hyperferritinemia associated with bi-allelic pathogenic variants of STAB1Edoardo Monfrini, Sara Pelucchi, Maija Hollmén, et al.
World Journal of Gastroenterology|June 22, 2012
Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosisLuca Valenti, Paolo Maggioni, Alberto Piperno, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|March 13, 2021
Prolonged exposure to welding fumes as a novel cause of systemic iron overloadRaffaella Mariani, Sara Pelucchi, Valentina Paolini, et al.
Haematologica|March 26, 2003
Prevalence of C282Y and E168X HFE mutations in an Italian population of Northern European ancestryAlessandra Salvioni, Raffaella Mariani, Christian Oberkanins, et al.
Journal of Hepatology|May 9, 2008
Hepcidin and iron-related gene expression in subjects with Dysmetabolic Hepatic Iron OverloadDonatella Barisani, Sara Pelucchi, Raffaella Mariani, et al.
Alzheimer Disease and Associated Disorders|September 5, 2009
Higher than expected progranulin mutation rate in a case series of Italian FTLD patientsLucio Tremolizzo, Giorgio Gelosa, Alessio Galbussera, et al.
American Journal of Hematology|February 8, 2020
Hyperferritinemia and diagnosis of type 1 Gaucher diseaseGiacomo Marchi, Fabio Nascimbeni, Irene Motta, et al.
EMBO Molecular Medicine|November 30, 2017
Ceruloplasmin replacement therapy ameliorates neurological symptoms in a preclinical model of aceruloplasminemiaAlan Zanardi, Antonio Conti, Marco Cremonesi, et al.
European Journal of Haematology|March 16, 2018
Hepcidin regulation in a mouse model of acute hypoxiaGiulia Ravasi, Sara Pelucchi, Gaia Buoli Comani, et al.
Pageof 10