A. Caleffi

发表

Juvenile hemochromatosis associated with pathogenic mutations of adult hemochromatosis genes.

W. Stremmel, F. Ferrara, P. Andreone, 2005, Gastroenterology.

Exome sequencing in a patient with Catel-Manzke-like syndrome excludes the involvement of the known genes and reveals a possible candidate.

E. Dassi, V. De Sanctis, R. Bertorelli, 2015, European journal of medical genetics.

Juvenile Hemochromatosis, Genetic Study and Long-term Follow up after Therapy

R. Malekzadeh, M. Akbari, A. Pietrangelo, 2014, Middle East journal of digestive diseases.

Iron Overload in the Liver of 2 Children: Nonalcoholic Steatohepatitis and Juvenile Hemochromatosis

G. Yılmaz, A. Pietrangelo, B. Dalgıç, 2017, Journal of pediatric hematology/oncology.

Lack of enterocyte iron accumulation in the ferroportin disease.

F. Ferrara, A. Pietrangelo, E. Corradini, 2005, Blood cells, molecules & diseases.

Human macrophage ferroportin biology and the basis for the ferroportin disease

S. Biffo, S. Oliveto, A. Pietrangelo, 2017, Hepatology.

Ferroportin-related haemochromatosis associated with novel Y64H mutation of the SCL40A1 gene

J. Raszeja-Wyszomirska, P. Milkiewicz, A. Pietrangelo, 2014, Przeglad gastroenterologiczny.

Non-HFE Hepatic Iron Overload

A. Pietrangelo, E. Corradini, A. Caleffi, 2011, Seminars in liver disease.

Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene.

R. Kittles, O. Onyekwere, O. Castro, 2003, Blood cells, molecules & diseases.

Ceruloplasmin gene variants are associated with hyperferritinemia and increased liver iron in patients with NAFLD.

S. Fargion, I. Bernardis, E. Tenedini, 2021, Journal of hepatology.

Keratin variants are overrepresented in primary biliary cirrhosis and associate with disease severity

M. Omary, Minhu Chen, C. Selmi, 2009, Hepatology.

G80S-linked ferroportin disease: the first clinical description in a Greek family.

A. Pietrangelo, A. Kourakli, M. Karakantza, 2008, Blood Cells, Molecules & Diseases.

Juvenile Hemochromatosis, Genetic Study and Long-term Follow up after Therapy

R. Malekzadeh, M. Akbari, A. Pietrangelo, 2014, Middle East journal of digestive diseases.

Erratum: Iron overload in Africans and African-Americans and a common mutation in the SCL40A1 (ferroportin 1) gene (Blood Cells, Molecules, and Diseases (2003) 31 (299-304) DOI: 10.1016/S1079-9796(03)00164-5)

R. Kittles, O. Onyekwere, O. Castro, 2004 .