G. Papanikolaou

发表

IL-6; A Possible Transformation Factor for Adenocarcinoma to Small Cell Lung Cancer. New Insights for IL-6 Targeted Therapy as an Adjuvant Treatment for NSCLC

L. Yarmus, Qiang Li, P. Zarogoulidis, 2013 .

The healing of colon anastomosis covered with fibrin glue after early postoperative intraperitoneal chemotherapy

G. Papanikolaou, 2006 .

Familial Mediterranean Fever and E148Q Pyrin Gene Mutation in Greece

K. Konstantopoulos, G. Papanikolaou, A. Kanta, 2005, International journal of hematology.

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

G. Sebastiani, K. Pantopoulos, J. Wagner, 2011, Hepatology.

Arthropathy in juvenile hemochromatosis.

D. Loukopoulos, G. Vaiopoulos, G. Papanikolaou, 2003, Arthritis and rheumatism.

Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.

D. Loukopoulos, C. Camaschella, S. Bosio, 2001, Blood cells, molecules & diseases.

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

Marie-Pierre Dubé, Elizabeta Nemeth, Tomas Ganz, 2004, Nature Genetics.

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

D. Loukopoulos, G. Papanikolaou, M. Politou, 2002, Blood cells, molecules & diseases.

Natural history of juvenile haemochromatosis

M. Cazzola, D. Girelli, P. Gasparini, 2002, British journal of haematology.

Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity.

E. Terpos, D. Loukopoulos, G. Papanikolaou, 2000, Blood cells, molecules & diseases.

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

C. Camaschella, A. Roetto, G. Papanikolaou, 2002, Blood cells, molecules & diseases.

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.

G. Papanikolaou, M. Politou, V. Kalotychou, 2004, Haematologica.

Hepcidin in iron overload disorders.

T. Ganz, Y. P. Goldberg, E. Nemeth, 2005, Blood.

Plantar Weight-Bearing Area Defects Reconstructed with Muscle Flap

A. Gravvanis, G. Papanikolaou, 2021, Clinical Scenarios in Reconstructive Microsurgery.

Plantar Weight-Bearing Area Defects Reconstructed with Perforator Flap

A. Gravvanis, G. Papanikolaou, 2021 .

Microvascular anastomotic aneurysms in the clinical setting: Case report and review of the literature

E. Lykoudis, G. Papanikolaou, N. Katsikeris, 2009, Microsurgery.

Iron metabolism and toxicity.

K. Pantopoulos, G. Papanikolaou, K Pantopoulos, 2005, Toxicology and applied pharmacology.

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

T. Spector, P. Deloukas, L. Kiemeney, 2017, Nature Communications.

Open Peer Review

G. Papanikolaou, David R. Holmes, Johns Hopkins, 2022 .

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

G. Tolis, G. Papanikolaou, A. Goula, 2005, Osteoporosis International.

Systemic iron homeostasis and erythropoiesis

K. Pantopoulos, G. Papanikolaou, 2017, IUBMB life.

Tamm-Horsfall protein in reflux nephropathy.

A. Howie, G. Papanikolaou, A. J. Arnold, 1995, Scandinavian journal of urology and nephrology.

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

I. Papassotiriou, A. Kattamis, F. Apostolakou, 2006, Haematologica.

Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

D. Girelli, D. Loukopoulos, C. Camaschella, 2003, Nature Genetics.

Regulation of iron transport and the role of transferrin.

K. Pantopoulos, G. Papanikolaou, K. Gkouvatsos, 2012, Biochimica et biophysica acta.

A Novel Immunological Assay for Hepcidin Quantification in Human Serum

D. Swinkels, G. Pangalis, E. Tsochatzis, 2009, PloS one.

Mineral intake.

S. Kanoni, G. Dedoussis, M. Stathopoulou, 2012, Progress in molecular biology and translational science.

Refining perforator selection for deep inferior epigastric perforator flap: The impact of the dominant venous perforator

D. Karakitsos, A. Gravvanis, D. Tsoutsos, 2014, Microsurgery.

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

I. Papassotiriou, D. Contopoulos-Ioannidis, I. Asproudis, 2006, Blood cells, molecules & diseases.

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

G. Papanikolaou, M. Politou, K. Polonifi, 2004, Haematologica.

A novel technique for precise placement and secure fixation of onlay grafts in rhinoplasty: our 4-year experience.

E. Lykoudis, G. Papanikolaou, K. Seretis, 2011, Plastic and reconstructive surgery.

Glucose Metabolism, Insulin Secretion and Insulin Sensitivity in Juvenile Hemochromatosis. A Case Report and Review of the Literature.

G. Tolis, M. Noutsou, G. Papanikolaou, 2006, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Congenital transmesosigmoid hernia: a rare case of pediatric small-bowel obstruction.

G. Alexiou, G. Papanikolaou, A. Kappas, 2008, Pediatric emergency care.