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Dimitris Loukopoulos

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Publications

TOP 3
Politou M; Zoi C; Dahabreh I J; Rallidis L; Gialeraki A; Loukopoulos D; Zoi K
No evidence of frequent association of the JAK2 V617F mutation with acute myocardial infarction in young patients.
Dahabreh Issa J; Jones Amy V; Voulgarelis Michael; Giannouli Stavroula; Zoi Christine; Alafakis-Tzannatos Christina; Varla-Leftherioti Marighoula; Moutsopoulos Haralampos M; Loukopoulos Dimitris; Fotiou Stelios; Cross Nicholas C P; Zoi Katerina
No evidence for increased prevalence of JAK2 V617F in women with a history of recurrent miscarriage.
Dahabreh Issa J; Zoi Katerina; Giannouli Stavroula; Zoi Christine; Loukopoulos Dimitrios; Voulgarelis Michael
Is JAK2 V617F mutation more than a diagnostic index? A meta-analysis of clinical outcomes in essential thrombocythemia.

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All Publications

2009: Politou M; Zoi C; Dahabreh I J; Rallidis L; Gialeraki A; Loukopoulos D; Zoi K
No evidence of frequent association of the JAK2 V617F mutation with acute myocardial infarction in young patients.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2009;23(5):1008-9.
2009: Dahabreh Issa J; Jones Amy V; Voulgarelis Michael; Giannouli Stavroula; Zoi Christine; Alafakis-Tzannatos Christina; Varla-Leftherioti Marighoula; Moutsopoulos Haralampos M; Loukopoulos Dimitris; Fotiou Stelios; Cross Nicholas C P; Zoi Katerina
No evidence for increased prevalence of JAK2 V617F in women with a history of recurrent miscarriage.
British journal of haematology 2009;144(5):802-3.
2009: Dahabreh Issa J; Zoi Katerina; Giannouli Stavroula; Zoi Christine; Loukopoulos Dimitrios; Voulgarelis Michael
Is JAK2 V617F mutation more than a diagnostic index? A meta-analysis of clinical outcomes in essential thrombocythemia.
Leukemia research 2009;33(1):67-73.
2008: Kouroupi Eirini; Zoi Katerina; Parquet Nathalie; Zoi Christine; Kiladjian Jean-Jacques; Grigoraki Vassiliki; Vainchenker William; Lellouche Franck; Marzac Christophe; Schlageter Marie-Hélène; Dosquet Christine; Scott Linda M; Fenaux Pierre; Loukopoulos Dimitris; Chomienne Christine; Cassinat Bruno
Mutations in exon 12 of JAK2 are mainly found in JAK2 V617F-negative polycythaemia vera patients.
British journal of haematology 2008;142(4):676-9.
2008: Zoi Katerina; Terpos Evangelos; Zoi Christine; Loukopoulos Dimitris
Increased CD177 (PRV1) expression in thalassaemia and the underlying erythropoietic activity.
British journal of haematology 2008;141(1):100-4.
2006: Koumbi Daphne; Clement Jean-Claude; Sideratou Zili; Yaouanc Jean-Jacques; Loukopoulos Dimitris; Kollia Panagoula
Factors mediating lipofection potency of a series of cationic phosphonolipids in human cell lines.
Biochimica et biophysica acta 2006;1760(8):1151-9.
2006: Voskaridou E; Terpos E; Michail S; Hantzi E; Anagnostopoulos A; Margeli A; Simirloglou D; Loukopoulos D; Papassotiriou I
Early markers of renal dysfunction in patients with sickle cell/beta-thalassemia.
Kidney international 2006;69(11):2037-42.
2005: Jones Amy V; Kreil Sebastian; Zoi Katerina; Waghorn Katherine; Curtis Claire; Zhang Lingyan; Score Joannah; Seear Rachel; Chase Andrew J; Grand Francis H; White Helen; Zoi Christine; Loukopoulos Dimitris; Terpos Evangelos; Vervessou Elisavet-Christine; Schultheis Beate; Emig Michael; Ernst Thomas; Lengfelder Eva; Hehlmann Rüdiger; Hochhaus Andreas; Oscier David; Silver Richard T; Reiter Andreas; Cross Nicholas C P
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders.
Blood 2005;106(6):2162-8.
2005: Voskaridou Ersi; Douskou Maroussa; Terpos Evangelos; Stamoulakatou Alexandra; Meletis John; Ourailidis Akis; Papassotiriou Ioannis; Loukopoulos Dimitris
Deferiprone as an oral iron chelator in sickle cell disease.
Annals of hematology 2005;84(7):434-40.
2004: Tsantes Argirios E; Papadhimitriou Stefanos I; Tassiopoulos Stergios T; Bonovas Stefanos; Paterakis George; Meletis Ioannis; Loukopoulos Dimitrios
Red cell macrocytosis in hypoxemic patients with chronic obstructive pulmonary disease.
Respiratory medicine 2004;98(11):1117-23.
2004: Voskaridou Ersi; Douskou Maroussa; Terpos Evangelos; Papassotiriou Ioannis; Stamoulakatou Alexandra; Ourailidis Akis; Loutradi Aphroditi; Loukopoulos Dimitris
Magnetic resonance imaging in the evaluation of iron overload in patients with beta thalassaemia and sickle cell disease.
British journal of haematology 2004;126(5):736-42.
2003: Voskaridou Ersi; Terpos Evangelos; Spina Giovanna; Palermos John; Rahemtulla Amin; Loutradi Aphroditi; Loukopoulos Dimitris
Pamidronate is an effective treatment for osteoporosis in patients with beta-thalassaemia.
British journal of haematology 2003;123(4):730-7.
2003: Tsantes Argirios E; Tassiopoulos Stergios T; Papadhimitriou Stefanos I; Bonovas Stefanos; Poulakis Nikolaos; Vlachou Athina; Filioussi Kalitsa; Loukopoulos Dimitrios
Theophylline treatment may adversely affect the anoxia-induced erythropoietic response without suppressing erythropoietin production.
European journal of clinical pharmacology 2003;59(5-6):379-83.
2003: Kalotychou Vassiliki; Antonatou Katerina; Tzanetea Revekka; Terpos Evaggelos; Loukopoulos Dimitris; Rombos Yannis
Analysis of the A(TA)(n)TAA configuration in the promoter region of the UGT1 A1 gene in Greek patients with thalassemia intermedia and sickle cell disease.
Blood cells, molecules & diseases 2003;31(1):38-42.
2003: Akel Salem; Mavroyanni Despina; Yataganas Xenophon; Terpos Evagelos; Meletis John; Anargyrou Kostas; Stavrogianni Niki; Pangalis Gerasimos-Alexander; Loukopoulos Dimitris; Viniou Nora
Clonal analysis of granulocyte-monocyte colony-forming unit cells with the human androgen receptor gene in chronic myeloid leukemia.
International journal of hematology 2003;77(5):476-81.
2003: Steinberg Martin H; Voskaridou Ersi; Kutlar Abdullah; Loukopoulos Dimitris; Koshy Mabel; Ballas Samir K; Castro Oswaldo; Barton Franca
Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease.
American journal of hematology 2003;72(2):121-6.
2003: Vaiopoulos George; Papanikolaou George; Politou Marianna; Jibreel Iyad; Sakellaropoulos Nikos; Loukopoulos Dimitris
Arthropathy in juvenile hemochromatosis.
Arthritis and rheumatism 2003;48(1):227-30.
2003: Roetto Antonella; Papanikolaou George; Politou Marianna; Alberti Federica; Girelli Domenico; Christakis John; Loukopoulos Dimitris; Camaschella Clara
Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis.
Nature genetics 2003;33(1):21-2.
2002: Gogas Helen; Paterakis George; Frangia Konstantina; Bafaloukos Dimitrios; Pectasides Dimitrios; Kalofonos Haralambos P; Loukopoulos Dimitrios; Stavropoulou-Giokas Cathrin; Ioannovich John; Mihm Martin C
Lymphocyte subpopulations and interleukin levels in high-risk melanoma patients treated with high-dose interferon A-2B.
American journal of clinical oncology 2002;25(6):591-6.
2002: Akel S; Kolialexi A; Mavrou A; Metaxotou C; Loukopoulos D; Yataganas X
Efficiency of interphase fluorescence in situ hybridization for BCR/ABL on peripheral blood smears for monitoring of CML patients: a comparison with bone marrow findings.
Clinical and laboratory haematology 2002;24(6):361-7.
2002: Papanikolaou G; Papaioannou M; Politou M; Vavatsi N; Kioumi A; Tsiatsiou P; Marinaki P; Loukopoulos D; Christakis J I
Genetic heterogeneity underlies juvenile hemochromatosis phenotype: analysis of three families of northern Greek origin.
Blood cells, molecules & diseases 2002;29(2):168-73.
2002: Aessopos A; Farmakis D; Loukopoulos D
Elastic tissue abnormalities in inherited haemolytic syndromes.
European journal of clinical investigation 2002;32(9):640-2.
2002: Gogas H; Kefala G; Bafaloukos D; Frangia K; Polyzos A; Pectasides D; Tsoutsos D; Panagiotou P; Ioannovich J; Loukopoulos D
Prognostic significance of the sequential detection of circulating melanoma cells by RT-PCR in high-risk melanoma patients receiving adjuvant interferon.
British journal of cancer 2002;87(2):181-6.
2002: Mavrogianni Despina; Viniou Nora; Michali Evi; Terpos Evangelos; Meletis John; Vaiopoulos George; Madzourani Marina; Pangalis Gerasimos; Yataganas Xenophon; Loukopoulos Dimitris
Leukemogenic risk of hydroxyurea therapy as a single agent in polycythemia vera and essential thrombocythemia: N- and K-ras mutations and microsatellite instability in chromosomes 5 and 7 in 69 patients.
International journal of hematology 2002;75(4):394-400.
2002: Viniou N; Terpos E; Galanopoulos A; Kritikou-Griva E; Akel S; Michalis E; Apostolidou E; Georgiadou D; Kouraklis A; Parharidou A; Kokkini G; Symeonidis A; Anagnostopoulos N I; Christakis J I; Tasiopoulou A; Loukopoulos D; Yataganas X
Treatment of anemia in low-risk myelodysplastic syndromes with amifostine. In vitro testing of response.
Annals of hematology 2002;81(4):182-6.
2002: Kalotychou Vassiliki; Kollia Panagoulia; Voskaridou Ersi; Patargias Theoharis; Anagnou Nicholas P; Loukopoulos Dimitris
Functional role of the four different types of (AT)(x)T(y) motifs 5' to the beta-globin gene and their distribution in the Greek population.
Blood cells, molecules & diseases 2002;28(1):39-46.
2002: Voskaridou Ersi; Terpos Evangelos; Komninaka Veroniki; Eftyhiadis Eftyhios; Mantzourani Marina; Loukopoulos Dimitris
Chronic myeloid leukaemia with marked thrombocytosis in a patient with thalassaemia major: complete haematological remission under the combination of hydroxyurea and anagrelide.
British journal of haematology 2002;116(1):155-7.
2002: Aessopos Athanasios; Farmakis Dimitrios; Loukopoulos Dimitris
Elastic tissue abnormalities resembling pseudoxanthoma elasticum in beta thalassemia and the sickling syndromes.
Blood 2002;99(1):30-5.
2002: Viniou Nora; Plata Eleni; Terpos Evangelos; Variami Eleni; Meletis John; Vaiopoulos George; Loukopoulos Dimitris; Chatzidimitriou Georgia; Yataganas Xenophon
Danazol therapy for thrombocytopenia in patients with myelodysplastic syndromes.
Acta haematologica 2002;107(4):234-6.
2002: Konstantopoulos Kostas; Agapitos Emmanouel; Komninaka Veroniki; Kritsova Vasso; Meletis John; Delaveris Emmanouel; Loukopoulos Dimitris
Acute Aspergillosis gastritis in a case of fatal aplastic anemia.
Scandinavian journal of infectious diseases 2002;34(2):148-9.
2001: Konstantopoulos K; Kanta A; Tzoulianos M; Dimou S; Sotsiou F; Politou M; Loukopoulos D
Familial Mediterranean fever phenotype II in Greece.
The Israel Medical Association journal : IMAJ 2001;3(11):862-3.
2001: Kollia P; Stavroyianni N; Stamatopoulos K; Zoi K; Viniou N; Mantzourani M; Noguchi C T; Paterakis G; Abazis D; Pangalos C; Loukopoulos D; Yataganas X
Molecular analysis of transferrin receptor mRNA expression in acute myeloid leukaemia.
British journal of haematology 2001;115(1):19-24.
2001: Aessopos A; Tsironi M; Vassiliadis I; Farmakis D; Fountos A; Voskaridou E; Perakis A; Defteraios S; Loutradi A; Loukopoulos D
Exercise-induced myocardial perfusion abnormalities in sickle beta-thalassemia: Tc-99m tetrofosmin gated SPECT imaging study.
The American journal of medicine 2001;111(5):355-60.
2001: Papanikolaou G; Politou M; Roetto A; Bosio S; Sakelaropoulos N; Camaschella C; Loukopoulos D
Linkage to chromosome 1q in Greek families with juvenile hemochromatosis.
Blood cells, molecules & diseases 2001;27(4):744-9.
2001: Marianna P; Kollia P; Akel S; Papassotiriou Y; Stamoulakatou A; Loukopoulos D
Valproic acid, trichostatin and their combination with hemin preferentially enhance gamma-globin gene expression in human erythroid liquid cultures.
Haematologica 2001;86(7):700-5.
2001: Konstantopoulos K; Psatha M; Kalotychou V; Frangia N; Ioannovits I; Meletis I; Loukopoulos D
Clinical significance of the molecular detection of melanoma cells circulating in the peripheral blood in melanoma patients.
Panminerva medica 2001;43(2):109-13.
2001: Aessopos A; Farmakis D; Karagiorga M; Voskaridou E; Loutradi A; Hatziliami A; Joussef J; Rombos J; Loukopoulos D
Cardiac involvement in thalassemia intermedia: a multicenter study.
Blood 2001;97(11):3411-6.
2001: Patrinos G P; Kollia P; Papapanagiotou E; Loutradi-Anagnostou A; Loukopoulos D; Papadakis M N
Agamma-haplotypes: a new group of genetic markers for thalassemic mutations inside the 5' regulatory region of the human Agamma-globin gene.
American journal of hematology 2001;66(2):99-104.
2001: Vaiopoulos G; Terpos E; Viniou N; Nodaros K; Rombos J; Loukopoulos D
Behcet's disease in a patient with chronic myelogenous leukemia under hydroxyurea treatment: a case report and review of the literature.
American journal of hematology 2001;66(1):57-8.
2001: Voskaridou E; Kyrtsonis M C; Terpos E; Skordili M; Theodoropoulos I; Bergele A; Diamanti E; Kalovidouris A; Loutradi A; Loukopoulos D
Bone resorption is increased in young adults with thalassaemia major.
British journal of haematology 2001;112(1):36-41.
2001: Meletis J; Terpos E; Samarkos M; Meletis C; Apostolidou E; Komninaka V; Korovesis K; Mavrogianni D; Boutsis D; Variami E; Viniou N; Konstantopoulos K; Loukopoulos D
Detection of CD55- and/or CD59-deficient red cell populations in patients with lymphoproliferative syndromes.
The hematology journal : the official journal of the European Haematology Association / EHA 2001;2(1):33-7.
2001: Meletis J; Terpos E; Samarkos M; Meletis C; Konstantopoulos K; Komninaka V; Apostolidou E; Benopoulou O; Korovesis K; Mavrogianni D; Variami E; Yataganas X; Loukopoulos D
Detection of CD55 and/or CD59 deficient red cell populations in patients with aplastic anaemia, myelodysplastic syndromes and myeloproliferative disorders.
Haematologia 2001;31(1):7-16.
2000: Loukopoulos D; Voskaridou E; Kalotychou V; Schina M; Loutradi A; Theodoropoulos I
Reduction of the clinical severity of sickle cell/beta-thalassemia with hydroxyurea: the experience of a single center in Greece.
Blood cells, molecules & diseases 2000;26(5):453-66.
2000: Akel S; Kolialexi A; Mavrou A; Metaxotou C; Loukopoulos D; Yataganas X
Evaluation at single cell level of residual Philadelphia negative hemopoietic stem cells in chronic phase CML patients.
Cancer genetics and cytogenetics 2000;122(2):93-100.
2000: Andreopoulos T; Papanikolaou G; Politou M; Konstantopoulos K; Stefanou J; Loukopoulos D
Micrococcus luteus: a putative cause of hepatic abscess?
Panminerva medica 2000;42(3):231-2.
2000: Papanikolaou G; Politou M; Terpos E; Fourlemadis S; Sakellaropoulos N; Loukopoulos D
Hereditary hemochromatosis: HFE mutation analysis in Greeks reveals genetic heterogeneity.
Blood cells, molecules & diseases 2000;26(2):163-8.
2000: Rombos Y; Tzanetea R; Konstantopoulos K; Simitzis S; Zervas C; Kyriaki P; Kavouklis M; Aessopos A; Sakellaropoulos N; Karagiorga M; Kalotychou V; Loukopoulos D
Chelation therapy in patients with thalassemia using the orally active iron chelator deferiprone (L1).
Haematologica 2000;85(2):115-7.
2000: Samarkos M; Aessopos A; Fragodimitri C; Karagiorga M; Kalotychou V; Voskaridou E; Kavouklis E; Loukopoulos D
Neutrophil elastase in patients with homozygous beta-thalassemia and pseudoxanthoma elasticum-like syndrome.
American journal of hematology 2000;63(2):63-7.
2000: Papassotiriou I; Voskaridou E; Stamoulakatou A; Loukopoulos D
Increased erythropoietin level induced by hydroxyurea treatment of sickle cell patients.
The hematology journal : the official journal of the European Haematology Association / EHA 2000;1(5):295-300.
1999: Stamatopoulos K; Kosmas C; Belessi C; Kyriazopoulos P; Papadaki T; Anagnostou D; Loukopoulos D
Molecular analysis of bcl-1/IgH junctional sequences in mantle cell lymphoma: potential mechanism of the t(11;14) chromosomal translocation.
British journal of haematology 1999;105(1):190-7.
1998: Papassotiriou I; Kister J; Griffon N; Stamoulakatou A; Abraham D J; Marden M C; Loukopoulos D; Poyart C
Modulating the oxygen affinity of human fetal haemoglobin with synthetic allosteric modulators.
British journal of haematology 1998;102(5):1165-71.
1998: Patrinos G P; Kollia P; Loutradi-Anagnostou A; Loukopoulos D; Papadakis M N
The Cretan type of non-deletional hereditary persistence of fetal hemoglobin [A gamma-158C-->T] results from two independent gene conversion events.
Human genetics 1998;102(6):629-34.
1998: Kollia P; Fibach E; Politou M; Noguchi C T; Schechter A N; Loukopoulos D
Hydroxyurea and hemin affect both the transcriptional and post-transcriptional mechanisms of some globin genes in human adult erythroid cells.
Annals of the New York Academy of Sciences 1998;850():449-51.
1998: Loukopoulos D; Voskaridou E; Stamoulakatou A; Papassotiriou Y; Kalotychou V; Loutradi A; Cozma G; Tsiarta H; Pavlides N
Hydroxyurea therapy in thalassemia.
Annals of the New York Academy of Sciences 1998;850():120-8.
1998: Kosmas C; Stamatopoulos K; Papadaki T; Belessi C; Yataganas X; Anagnostou D; Loukopoulos D
Somatic hypermutation of immunoglobulin variable region genes: focus on follicular lymphoma and multiple myeloma.
Immunological reviews 1998;162():281-92.
1998: Aessopos A; Samarkos M; Voskaridou E; Papaioannou D; Tsironi M; Kavouklis E; Vaiopoulos G; Stamatelos G; Loukopoulos D
Arterial calcifications in beta-thalassemia.
Angiology 1998;49(2):137-43.
1998: Meletis J; Samarkos M; Mesogitis S; Meletis C; Mougiou A; Terpos E; Tsimberidou A; Andreopoulos A; Konstantopoulos K; Loukopoulos D
Severe aplastic anaemia relapsing during a pregnancy; spontaneous remission following termination.
Haematologia 1998;29(2):147-51.
1997: Meletis J; Michali E; Samarkos M; Konstantopoulos K; Meletis C; Terpos E; Tsimberidou A; Chandrinou E; Viniou N; Rombos Y; Pangalis G A; Yataganas X; Loukopoulos D
Detection of "PNH red cell" populations in hematological disorders using the Sephacryl Gel Test micro typing system.
Leukemia & lymphoma 1997;28(1-2):177-82.
1997: Stamatopoulos K; Kosmas C; Belessi C; Papadaki T; Afendaki S; Anagnostou D; Loukopoulos D
t(14;18) chromosomal translocation in follicular lymphoma: an event occurring with almost equal frequency both at the D to J(H) and at later stages in the rearrangement process of the immunoglobulin heavy chain gene locus.
British journal of haematology 1997;99(4):866-72.
1997: Kosmas C; Stamatopoulos K; Loukopoulos D
Antigen selection of multiple myeloma clonogenic B cells as evidenced by V(H) and V(L) gene mutations.
Blood 1997;90(3):1334-5.
1997: Kollia P; Noguchi C T; Fibach E; Loukopoulos D; Schechter A N
Modulation of globin gene expression in cultured erythroid precursors derived from normal individuals: transcriptional and posttranscriptional regulation by hemin.
Proceedings of the Association of American Physicians 1997;109(4):420-8.
1997: Viniou N; Abazis D; Yataganas X; Benkhalifa M; Stamatopoulos K; Vayopoulos G; Plata E; Loukopoulos D; Pangalos C
A novel chromosomal abnormality involving chromosomes 2 and 18 in a patient with myelodysplastic syndrome.
Cancer genetics and cytogenetics 1997;96(1):7-12.
1997: Viniou N; Michali E; Meletis J; Andreopoulos A; Vaiopoulos G; Stavroyianni N; Loukopoulos D; Yataganas X
Trisomy 8 in a patient who responded to therapy with all-trans-retinoic acid and developed paroxysmal nocturnal haemoglobinuria.
British journal of haematology 1997;97(1):135-6.
1997: Stamatopoulos K; Kosmas C; Papadaki T; Pouliou E; Belessi C; Afendaki S; Anagnostou D; Loukopoulos D
Follicular lymphoma immunoglobulin kappa light chains are affected by the antigen selection process, but to a lesser degree than their partner heavy chains.
British journal of haematology 1997;96(1):132-46.
1997: Tassiopoulos T; Konstantopoulos K; Tassiopoulos S; Rombos Y; Alevizou-Terzaki V; Kyriaki P; Loukopoulos D
Erythropoietin levels and microcytosis in heterozygous beta-thalassaemia.
Acta haematologica 1997;98(3):147-9.
1997: Loukopoulos D
New therapies for the haemoglobinopathies.
Journal of internal medicine. Supplement 1997;740():43-8.
1996: Mantzourani M; Stamatopoulos K; Abazis D; Kontopidou F; Viniou N; Pangalis G A; Pangalos C; Loukopoulos D
Molecular demonstration of BCR/ABL fusion in two cases with chronic myeloproliferative disorder carrying variant Philadelphia t(14;22)(q32;q11).
Cancer genetics and cytogenetics 1996;91(1):82-7.
1996: Stamatopoulos K; Kosmas C; Stavroyianni N; Loukopoulos D
Evidence for immunoglobulin heavy chain variable region gene replacement in a patient with B cell chronic lymphocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(9):1551-6.
1996: Kosmas C; Viniou N A; Stamatopoulos K; Courtenay-Luck N S; Papadaki T; Kollia P; Paterakis G; Anagnostou D; Yataganas X; Loukopoulos D
Analysis of the kappa light chain variable region in multiple myeloma.
British journal of haematology 1996;94(2):306-17.
1996: Vaiopoulos G; Viniou N; Plata E; Konstantopoulos K; Andreopoulos A; Rombos Y; Meletis J; Loukopoulos D; Yataganas X
Development of plasma cell tumors during treatment of multiple myeloma.
Annals of hematology 1996;72(5):317-20.
1996: Paterakis G S; Tsavaris N; Loukopoulos D
The effect of GM-CSF on reticulocytes, haemoglobin and haematocrit in patients receiving chemotherapy for solid tumours.
Clinical and laboratory haematology 1996;18(1):7-12.
1996: Aessopos A; Samarcos M; Hadjinikolaou P; Vaiopoulos G; Skoumas V; Kolainis I; Loukopoulos D
Myocardial infarction with normal coronary arteries in S/beta thalassaemia patients.
European heart journal 1996;17(2):317-8.
1996: Loukopoulos D
Current status of thalassemia and the sickle cell syndromes in Greece.
Seminars in hematology 1996;33(1):76-86.
1996: Meletis J; Samarkos M; Abazis D; Michali E; Vavourakis S; Plata E; Rombos J; Konstantopoulos K; Pangalos K; Yataganas X; Loukopoulos D
Trisomy 11 with loss of the Y chromosome and trisomy 13 in a case of de novo acute myeloid leukemia.
Cancer genetics and cytogenetics 1996;86(1):65-8.
1995: Konstantopoulos K; Androulaki A; Aessopos A; Patsouris E; Dosios T H; Psychogios A; Loukopoulos D
Pure red cell aplasia associated with true thymic hyperplasia.
Human pathology 1995;26(10):1160-2.
1995: Rombos Y; Tassiopoulos T; Tzanetea R; Tsekoura C; Loukopoulos D
Clinical improvement of beta-Thal-HbS anemia by iron deficiency.
American journal of hematology 1995;50(1):68-9.
1995: Konstantopoulos K; Delladetsima I; Kosmas C; Androulaki A; Stamatopoulos K; Rekoumi L; Patsouris S; Loukopoulos D
Diffuse hepatic calcinosis and hypercalcemia in association with a B-cell (centroblastic) lymphoma.
American journal of hematology 1995;50(1):67.
1995: Viniou N A; Matzourani M; Yataganas X; Meletis J; Pangalis G; Loukopoulos D
Correlation of the site of M-bcr breakpoint with chronic phase duration, blastic crisis lineage and thrombocytosis in Ph1-positive chronic myelogenous leukemia.
Leukemia & lymphoma 1995;18(3-4):335-9.
1995: Voskaridou E; Konstantopoulos K; Kollia P; Papadakis M; Loukopoulos D
Hb Lepore (Pylos)/Hb S compounds heterozygosity in two Greek families.
American journal of hematology 1995;49(2):131-4.
1995: Viniou N; Yataganas X; Abazis D; Paterakis G; Vavourakis S; Stamatopoulos K; Matzourani M; Loukopoulos D; Pangalos C
Hypereosinophilia associated with monosomy 7.
Cancer genetics and cytogenetics 1995;80(1):68-71.
1995: Voskaridou E; Kalotychou V; Loukopoulos D
Clinical and laboratory effects of long-term administration of hydroxyurea to patients with sickle-cell/beta-thalassaemia.
British journal of haematology 1995;89(3):479-84.
1995: Mantzourani M; Konstantopoulos K; Voskaridou E; Loukopoulos D
Molecular genetics of "X-linked" sideroblastic anemia.
American journal of hematology 1995;48(2):131.
1995: Konstantopoulos K; Androulaki A; Voskaridou E; Archontis E; Kosmopoulou O; Mantzourani M; Dosios T; Karakitsos P; Patsouris E; Loukopoulos D
Accelerated phase of chronic myeloid leukemia presenting as pericadial extramedullary hematopoiesis.
Annals of hematology 1995;70(1):43-5.
1995: Aessopos A; Stamatelos G; Skoumas V; Vassilopoulos G; Mantzourani M; Loukopoulos D
Pulmonary hypertension and right heart failure in patients with beta-thalassemia intermedia.
Chest 1995;107(1):50-3.
1995: Vaiopoulos G; Konstantopoulos K; Kittas C; Hatzakis A; Bogdanos K; Mastrovassilopoulos A; Meletis J; Loukopoulos D
Histological and functional changes in the salivary glands in thalassaemia major.
Haematologia 1995;27(1):33-8.
1995: Konstantopoulos K; Plataniotis G; Maris T; Voskaridou E; Rekoumi L; Stratigaki M; Loukopoulos D
Extramedullary haemopoiesis in thalassaemia intermedia: an unusual case of relapsing paraparesis in pregnancy.
Haematologia 1995;27(1):29-32.
1994: Balassopoulou A; Papadakis M; Loukopoulos D
A novel nonsense mutation identified in the first nucleotide binding fold of the CFTR gene in a Greek patient.
Human molecular genetics 1994;3(10):1887-8.
1994: Paterakis G S; Laoutaris N P; Alexia S V; Siourounis P V; Stamulakatou A K; Premetis E E; Sakellariou C; Terzoglou G N; Papassotiriou I G; Loukopoulos D
The effect of red cell shape on the measurement of red cell volume. A proposed method for the comparative assessment of this effect among various haematology analysers.
Clinical and laboratory haematology 1994;16(3):235-45.
1994: Paterakis G; Konstantopoulos K; Loukopoulos D
Spuriously increased platelet count due to microcyte interference: value of the R-1000 (Sysmex) reticulocyte analyzer.
American journal of hematology 1994;46(1):57-8.
1994: Aessopos A; Voskaridou E; Kavouklis E; Vassilopoulos G; Rombos Y; Gavriel L; Loukopoulos D
Angioid streaks in sickle-thalassemia.
American journal of ophthalmology 1994;117(5):589-92.
1994: Konstantopoulos K; Kasparian T; Sideris J; Voskaridou E; Loukopoulos D
Mechanical hemolysis associated with a bioprosthetic mitral valve combined with a calcified aortic valve stenosis.
Acta haematologica 1994;91(3):164-5.
1994: Konstantopoulos K; Avlami A; Demarongona K; Sideris G; Rekoumi L; Stefanou J; Voskaridou E; Loukopoulos D
Bacteroides fragilis arthritis in a sickle cell-thalassaemia patient.
Scandinavian journal of infectious diseases 1994;26(4):495-7.
1994: Viniou N; Georgiou J; Loutradi A; Rombos J; Fessas P; Loukopoulos D
Molecular basis and haplotype analysis of delta, beta-thalassemic chromosomes in Greece.
Acta haematologica 1994;92(2):83-7.
1993: Meletis J; Vavourakis S; Andreopoulos T; Yataganas X; Poziopoulos C; Lafioniatis S; Konstantopoulos K; Loukopoulos D
Recovery of carbimazole-induced agranulocytosis following recombinant granulocyte-macrophage colony stimulating factor (rhGM-CSF) administration.
Haematologica 1993;78(5):329-31.
1993: Paterakis G S; Lykopoulou L; Papassotiriou J; Stamulakatou A; Kattamis C; Loukopoulos D
Flow-cytometric analysis of reticulocytes in normal cord blood.
Acta haematologica 1993;90(4):182-5.
1992: Kollia P; Karababa P H; Sinopoulou K; Voskaridou E; Boussiou M; Papadakis M; Loukopoulos D
Beta-thalassaemia mutations and the underlying beta gene cluster haplotypes in the Greek population.
Gene geography : a computerized bulletin on human gene frequencies 1992;6(1-2):59-70.
1991: Paterakis G S; Voskaridou E; Loutradi A; Rombos J; Loukopoulos D
Reticulocyte counting in thalassemic and other conditions with the R-1000 Sysmex analyzer.
Annals of hematology 1991;63(4):218-22.
1991: Jankovic L; Dimovski A J; Kollia P; Karageorga M; Loukopoulos D; Huisman T H
A C----G mutation at nt position 6 3' to the terminating codon may be the cause of a silent beta-thalassemia.
International journal of hematology 1991;54(4):289-93.
1991: Loukopoulos D
Thalassemia: genotypes and phenotypes.
Annals of hematology 1991;62(5):145-50.
1991: Loudianos G; Cao A; Pirastu M; Vassilopoulos G; Kollia P; Loukopoulos D
Molecular basis of the delta thalassemia in cis to hemoglobin Knossos variant.
Blood 1991;77(9):2087-8.
1991: Loukopoulos D
Thalassemia: genotypes and phenotypes.
Annals of hematology 1991;62(4):85-94.
1991: Christakis J; Vavatsi N; Hassapopoulou H; Angeloudi M; Papadopoulou M; Loukopoulos D; Morris J S; Serjeant B E; Serjeant G R
A comparison of sickle cell syndromes in northern Greece.
British journal of haematology 1991;77(3):386-91.
1991: Boussiou M; Loukopoulos D; Christakis J; Fessas P
The origin of the sickle mutation in Greece; evidence from beta S globin gene cluster polymorphisms.
Hemoglobin 1991;15(6):459-67.
1990: Balassopoulou A; Loukopoulos D; Kollia P; Devoto M; Adam G; Arvanitakis S; Hadjisevastou H
Cystic fibrosis in Greece: typing with DNA probes and identification of the common molecular defect.
Human genetics 1990;85(4):393-4.
1990: Christakis J; Vavatsi N; Hassapopoulou H; Papadopoulou M; Mandraveli K; Loukopoulos D; Morris J S; Serjeant B E; Serjeant G R
Comparison of homozygous sickle cell disease in northern Greece and Jamaica.
Lancet 1990;335(8690):637-40.
1990: Loukopoulos D; Hadji A; Papadakis M; Karababa P; Sinopoulou K; Boussiou M; Kollia P; Xenakis M; Antsaklis A; Mesoghitis S
Prenatal diagnosis of thalassemia and of the sickle cell syndromes in Greece.
Annals of the New York Academy of Sciences 1990;612():226-36.
1990: Lymberi P; Aessopos A; Karageorga M; Hadzigianni D; Loukopoulos D; Kaklamanis P
Increased IgA natural autoantibody activity in sera of patients with homozygous beta-thalassaemia.
Autoimmunity 1990;8(1):81-2.
1989: Galacteros F; Loukopoulos D; Fessas P; Kister J; Arous N; Bohn B; Loutradi A; Tsitrakis G; Poyart C
Hemoglobin Köln occurring in association with a beta zero thalassemia: hematologic and functional consequences.
Blood 1989;74(1):496-500.
1989: Kollia P; Gonzalez-Redondo J M; Stoming T A; Loukopoulos D; Politis C; Huisman T H
Frameshift codon 5 [Fsc-5 (-CT)] thalassemia; a novel mutation detected in a Greek patient.
Hemoglobin 1989;13(6):597-604.
1988: Loukopoulos D; Kaltsoya-Tassiopoulou A; Fessas P
Thalassemia control in Greece.
Birth defects original article series 1988;23(5B):405-16.
1986: Loukopoulos D; Poyart C; Delanoe-Garin J; Matsis C; Arous N; Kister J; Loutradi-Anagnostou A; Blouquit Y; Fessas P; Thillet J
Hemoglobin San Diego/beta zero thalassemia in a Greek adult.
Hemoglobin 1986;10(2):143-59.
1985: Meletis J; Yataganas X; Eliopoulos G; Panourgias J; Loukopoulos D; Fessas P
Hemoglobin content of single erythrocytes from fetuses with parents having heterozygous beta-thalassemia.
Acta haematologica 1985;73(1):16-21.
1985: Yataganas X; Meletis J; Loukopoulos D; Fessas P
The hemoglobin content and concentration of single fetal erythrocytes obtained by placentocentesis from mothers with heterozygous beta-thalassemia.
Annals of the New York Academy of Sciences 1985;445():376-9.
1985: Tassiopoulos T; Fessas P; Rombos J; Loukopoulos D
Observations on oxygen delivery, methemoglobinemia, and arterial oxygenation in patients with beta-thalassemia.
Annals of the New York Academy of Sciences 1985;445():135-47.
1985: Loukopoulos D; Karababa P; Antsaklis A; Panourgias J; Boussiou M; Karayannopoulos K; Politis J; Rombou D; Kaltsoya-Tassiopoulou A; Fessas P
Prenatal diagnosis of thalassemia and Hb S syndromes in Greece: an evaluation of 1500 cases.
Annals of the New York Academy of Sciences 1985;445():357-75.
1984: Antsaklis A; Politis J; Karagiannopoulos C; Kaskarelis D; Karababa P; Panourgias J; Boussiou M; Loukopoulos D
Selective survival of only the healthy fetus following prenatal diagnosis of thalassaemia major in binovular twin gestation.
Prenatal diagnosis 1984;4(4):289-96.
1984: Dash S; Panourgias J; Karababa P; Loukopoulos D
Prenatal diagnosis of thalassaemia by haemoglobin chromatography on Biorex. An evaluation of the method.
Prenatal diagnosis 1984;4(1):11-20.
1983: Loukopoulos D; Kaltsoya-Tassiopoulou A; Fessas P
Prevention of thalassemia.
Schweizerische medizinische Wochenschrift 1983;113(40):1419-27.
1983: Antsaklis A; Papantoniou N; Loukopoulos D; Kaskarelis D
Prenatal diagnosis of hemoglobinopathies in twin pregnancies by double simultaneous fetoscopy.
Prenatal diagnosis 1983;3(1):21-7.
1983: Rosa J; Fessas P; Galacteros F; Monplaisir N; Loukopoulos D; Blouquit Y; Komis G; Arous N; Boussiou M
Hb Knossos, beta 27 Ala leads to Ser (B 9): a new hemoglobinopathy presenting as a silent beta-thalassemia.
Progress in clinical and biological research 1983;134():129-30.
1983: Tassiopoulos T; Fessas P; Pangalis G; Andreopoulos A; Loukopoulos D
[Erythrocyte volume and 2,3-DPG level. A study on a primary polycythemia model]
Nouvelle revue française d'hématologie 1983;25(4):263-6.
1982: Arous N; Galacteros F; Fessas P; Loukopoulos D; Blouquit Y; Komis G; Sellaye M; Boussiou M; Rosa J
Structural study of hemoglobin Knossos, beta 27 (B9) Ala leads to Ser. A new abnormal hemoglobin present as a silent beta-thalassemia.
FEBS letters 1982;147(2):247-50.
1982: Fessas P; Loukopoulos D; Loutradi-Anagnostou A; Komis G
'Silent' beta-thalassaemia caused by a 'silent' beta-chain mutant: the pathogenesis of a syndrome of thalassaemia intermedia.
British journal of haematology 1982;51(4):577-83.
1982: Loukopoulos D; Antsaklis A; Aleporou-Marinou V; Panourgias J; Karababa P; Fessas P
Prenatal diagnosis of beta-thalassemia; the greek experience.
Birth defects original article series 1982;18(7):293-301.
1980: Kaltsoya-Tassiopoulou A; Zoumbos N; Loukopoulos D; Fessas P; Kattamis C; Metaxotou-Mavromati A; Wood W G; Weatherall D J
'Silent' beta thalassaemia and normal HbA2 beta thalassaemia.
British journal of haematology 1980;45(1):177-8.

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