Search Results - "Lilakos, K"

FLT3 Overexpression in Acute Promyelocytic Leukemia Patients without Detectable FLT3-ITD or Codon 835-836 Mutations: A Pilot Study by LILAKOS, K, VINIOU, N. A, XILOURI, I, GALANOPOULOS, A, AGELOUDI, M, PANAYIOTID S, P, VOULGARELIS, M, ROMBOS, J, MELETIS, J, YATAGANAS, X, PANGALIS, G. A, MAVROGIANNI, D, VASSILAKOPOULOS, T. P, DIMOPOULOU, M. N, PLATA, E, ANGELOPOULOU, M. K, VARIAMI, E, STAVROGIANNI, N, LIAPI, D

“…Background: Activating mutations of the FLT3 receptor tyrosine kinase are common in acute promyelocytic leukemia (APL) but have uncertain prognostic…”
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Serum ceruloplasmin as a marker in prostate cancer by Fotiou, K, Vaiopoulos, G, Lilakos, K, Giannopoulos, A, Mandalenaki, K, Marinos, G, Koritsiadis, G, Sourdis, J, Konstantinidou, E, Konstantopoulos, K

“…Serum acid phosphatase and prostate specific antigen have been utilized as disease markers in prostate cancer, one of the commonest cancers of the elderly…”
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Abstract P4-04-10: Clinically relevant tumor mutation profiles in patients with triple negative breast cancer (TNBC) by Kotoula, V, Lilakos, K, Timotheadou, E, Dimopoulos, MA, Christodoulou, C, Pentheroudakis, G, Gogas, H, Charalambous, E, Papadopoulou, K, Gkakou, C, Lakis, S, Kalogeras, KT, Pectasides, D, Fountzilas, G

“…Abstract TNBC account for ∼15% of breast cancers and are most difficult to treat. However, TNBC patient outcome is very heterogeneous. In an effort to…”
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Clonal expansion of B-cells in human systemic lupus erythematosus: Evidence from studies before and after therapeutic B-cell depletion by Sfikakis, Petros P, Karali, Vassiliki, Lilakos, Konstantinos, Georgiou, George, Panayiotidis, Panayiotis

“…Abstract Anti-B-cell therapy may be beneficial for patients with SLE and active proliferative glomerulonephritis. Using genomic DNA, we examined how…”
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Familial Mediterranean fever and E148Q pyrin gene mutation in Greece by KONSTANTOPOULOS, Kostas, KANTA, Alexandra, LILAKOS, Konstantinos, PAPANIKOLAOU, George, MELETIS, Ioannis

“…Familial Mediterranean fever (FMF) is an inherited disease characterized by recurrent inflammatory polyserositis. Although FMF is classically expected only in…”
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Prevalence of the G320V mutation of the HJV gene, associated with juvenile hemochromatosis, in Greece by Pissia, M, Polonifi, K, Politou, M, Lilakos, K, Sakellaropoulos, N, Papanikolaou, G

“…Mutations of the HJV gene, which maps on chromosome 1q21, underlie most cases of juvenile hemochromatosis. We evaluated the frequency of the most common…”
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Hereditary hyperferritinemia cataract syndrome in three unrelated families of western Greek origin caused by the C39 > G mutation of L-ferritin IRE by Papanikolaou, George, Chandrinou, Helen, Bouzas, Evrydiki, Contopoulos-Ioannidis, Despina, Kalotychou, Vassiliki, Prentzas, Konstantinos, Lilakos, Konstantinos, Asproudis, Ioannis, Palaiologou, Danai, Premetis, Evangelos, Papassotiriou, Ioannis, Sakellaropoulos, Nikos

“…Hereditary hyperferritinemia–cataract syndrome (HHCS) is a well-characterized autosomal dominant disease caused by mutations in the iron responsive element…”
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