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56 results
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Development and evaluation of a tablet-based diagnostic audiometer.
Thoidis I, Vrysis L, Markou K, Papanikolaou G. Thoidis I, et al. Among authors: papanikolaou g. Int J Audiol. 2019 Aug;58(8):476-483. doi: 10.1080/14992027.2019.1600204. Epub 2019 Apr 15. Int J Audiol. 2019. PMID: 30987489
Long-term signal detection, segmentation and summarization using wavelets and fractal dimension: a bioacoustics application in gastrointestinal-motility monitoring.
Dimoulas C, Kalliris G, Papanikolaou G, Kalampakas A. Dimoulas C, et al. Among authors: papanikolaou g. Comput Biol Med. 2007 Apr;37(4):438-62. doi: 10.1016/j.compbiomed.2006.08.013. Epub 2006 Oct 4. Comput Biol Med. 2007. PMID: 17026978
Application of Glottal Disturbogram as a novel tool for the description of vocal disturbances.
Pastiadis C, Papanikolaou G, Printza A. Pastiadis C, et al. Among authors: papanikolaou g. Hippokratia. 2008 Apr;12(2):122-7. Hippokratia. 2008. PMID: 18923662 Free PMC article.
Arthropathy in juvenile hemochromatosis.
Vaiopoulos G, Papanikolaou G, Politou M, Jibreel I, Sakellaropoulos N, Loukopoulos D. Vaiopoulos G, et al. Among authors: papanikolaou g. Arthritis Rheum. 2003 Jan;48(1):227-30. doi: 10.1002/art.10755. Arthritis Rheum. 2003. PMID: 12528123
Osteoporosis in HFE2 juvenile hemochromatosis. A case report and review of the literature.
Angelopoulos NG, Goula AK, Papanikolaou G, Tolis G. Angelopoulos NG, et al. Among authors: papanikolaou g. Osteoporos Int. 2006 Jan;17(1):150-5. doi: 10.1007/s00198-005-1920-6. Epub 2005 Jul 5. Osteoporos Int. 2006. PMID: 15997423 Review.
Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis.
Papanikolaou G, Samuels ME, Ludwig EH, MacDonald ML, Franchini PL, Dubé MP, Andres L, MacFarlane J, Sakellaropoulos N, Politou M, Nemeth E, Thompson J, Risler JK, Zaborowska C, Babakaiff R, Radomski CC, Pape TD, Davidas O, Christakis J, Brissot P, Lockitch G, Ganz T, Hayden MR, Goldberg YP. Papanikolaou G, et al. Nat Genet. 2004 Jan;36(1):77-82. doi: 10.1038/ng1274. Epub 2003 Nov 30. Nat Genet. 2004. PMID: 14647275
Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE.
Papanikolaou G, Chandrinou H, Bouzas E, Contopoulos-Ioannidis D, Kalotychou V, Prentzas K, Lilakos K, Asproudis I, Palaiologou D, Premetis E, Papassotiriou I, Sakellaropoulos N. Papanikolaou G, et al. Blood Cells Mol Dis. 2006 Jan-Feb;36(1):33-40. doi: 10.1016/j.bcmd.2005.10.003. Epub 2006 Jan 5. Blood Cells Mol Dis. 2006. PMID: 16406710
The effects of erythropoetic activity and iron burden on hepcidin expression in patients with thalassemia major.
Kattamis A, Papassotiriou I, Palaiologou D, Apostolakou F, Galani A, Ladis V, Sakellaropoulos N, Papanikolaou G. Kattamis A, et al. Among authors: papanikolaou g. Haematologica. 2006 Jun;91(6):809-12. Haematologica. 2006. PMID: 16769583
Hepcidin in iron overload disorders.
Papanikolaou G, Tzilianos M, Christakis JI, Bogdanos D, Tsimirika K, MacFarlane J, Goldberg YP, Sakellaropoulos N, Ganz T, Nemeth E. Papanikolaou G, et al. Blood. 2005 May 15;105(10):4103-5. doi: 10.1182/blood-2004-12-4844. Epub 2005 Jan 25. Blood. 2005. PMID: 15671438 Free PMC article.
Familial Mediterranean fever and E148Q pyrin gene mutation in Greece.
Konstantopoulos K, Kanta A, Lilakos K, Papanikolaou G, Meletis I. Konstantopoulos K, et al. Among authors: papanikolaou g. Int J Hematol. 2005 Jan;81(1):26-8. doi: 10.1532/ijh97.e0422. Int J Hematol. 2005. PMID: 15717684
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