List of works - George Papanikolaou

A novel immunological assay for hepcidin quantification in human serum

scientific article

Arthropathy in juvenile hemochromatosis

scientific article published on 01 January 2003

Commentary: Juvenile hemochromatosis in a Spanish family (by Montes-Cano et al.).

scientific article published on 01 July 2002

Conditional disruption of mouse HFE2 gene: maintenance of systemic iron homeostasis requires hepatic but not skeletal muscle hemojuvelin

scientific article published on 24 August 2011

Ethical Issues and Barriers for Multi-National Paediatric Clinical Trials: The Challenging Experience of the DEEP Project ⬇️

scholarly article

Expression of three different ATP-binding cassette transporters and correlation to chemoresistance in acute myeloid leukemia

scientific article published on 09 May 2014

Familial Mediterranean fever and E148Q pyrin gene mutation in Greece

scientific article published on January 2005

Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin

scientific article published on 01 September 2002

Hepcidin in iron overload disorders

scientific article published on 25 January 2005

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity

scientific article published in April 2000

Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE

scientific article published on 05 January 2006

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis

scientific article published on 01 July 2001

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

scientific article

Mineral intake

scientific article published on January 2012

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

scientific article

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

scientific article (publication date: 2004)

Natural history of juvenile haemochromatosis

scientific article

Osteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature.

scientific article

Prevalence of the G320V mutation of the HJV gene, associated with juvenile hemochromatosis, in Greece

scientific article published in June 2004

Regulation of iron transport and the role of transferrin

scientific article

Systemic iron homeostasis and erythropoiesis

scientific article published on 6 April 2017

The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major.

scientific article

The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients

scientific article published in April 2004

List of works by George Papanikolaou

A novel immunological assay for hepcidin quantification in human serum

Arthropathy in juvenile hemochromatosis

Commentary: Juvenile hemochromatosis in a Spanish family (by Montes-Cano et al.).

Conditional disruption of mouse HFE2 gene: maintenance of systemic iron homeostasis requires hepatic but not skeletal muscle hemojuvelin

Ethical Issues and Barriers for Multi-National Paediatric Clinical Trials: The Challenging Experience of the DEEP Project ⬇️

Expression of three different ATP-binding cassette transporters and correlation to chemoresistance in acute myeloid leukemia

Familial Mediterranean fever and E148Q pyrin gene mutation in Greece

Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin

Hepcidin in iron overload disorders

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity

Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis

Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness

Mineral intake

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis

Natural history of juvenile haemochromatosis

Osteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature.

Prevalence of the G320V mutation of the HJV gene, associated with juvenile hemochromatosis, in Greece

Regulation of iron transport and the role of transferrin

Systemic iron homeostasis and erythropoiesis

The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major.

The impact of the mutations of the HFE gene and of the SLC11A3 gene on iron overload in Greek thalassemia intermedia and beta(s)/beta(thal) anemia patients