Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Evi Michali"'
Autor:
Niki Stavrogianni, Christos Poziopoulos, Christos Meletis, Evi Michali, Stathis Vavourakis, John Meletis, Kostas Konstantopoulos, George Vaiopoulos, Michalis Samarkos, Xenophon Yataganas, Dimitris Loukopoulos
Publikováno v:
British Journal of Haematology. 89:911-913
A case of adult osteopetrosis Type I was diagnosed in a 22-year-old female. She presented for investigation of anaemia with 'myelophthisic' characteristics and extramedullary haemopoiesis which was resistant to haematinics, nandrolone and low-dose co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae0258c60d3bada890ddc1f189ab6c2c
https://doi.org/10.1111/j.1365-2141.1995.tb08436.x
https://doi.org/10.1111/j.1365-2141.1995.tb08436.x
Autor:
Kostas Konstantopoulos, Yannis Rombos, Eleni Chandrinou, Evangelos Terpos, Evi Michali, Xenophon Yataganas, Apostolia Maria Tsimberidou, Dimitris Loukopoulos, Christos Meletis, Gerassimos A. Pangalis, Nora Viniou, John Meletis, Michalis Samarkos
Publikováno v:
Leukemia & Lymphoma. 28:177-182
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal disorder characterised by an unusual sensitivity of abnormal red cell population(s) to complement lysis, due to a complete or incomplete defect of various surface molecules, including CD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8923b42fe5e3f3bc3f847a0f8896c35e
https://doi.org/10.3109/10428199709058344
https://doi.org/10.3109/10428199709058344
Autor:
Dimitris Loukopoulos, Despina Mavrogianni, Gerasimos Pangalis, John Meletis, Nora Viniou, Evi Michali, Evangelos Terpos, Xenophon Yataganas, George Vaiopoulos, Marina Madzourani
Publikováno v:
International journal of hematology. 75(4)
Polycythemia vera (PV) and essential thrombocythemia (ET) are chronic myeloproliferative diseases that carry intrinsically the potential for leukemic transformation. The aims of this study were (1) to detect involvement of N- and K-ras mutations in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41726588ea06cb84ad87e3fcf09ba6da
https://pubmed.ncbi.nlm.nih.gov/12041671
https://pubmed.ncbi.nlm.nih.gov/12041671
Autor:
Stathis Vavourakis, Kostas Konstantopoulos, Xenophon Yataganas, Dimitris Loukopoulos, Konstantinos Pangalos, Michalis Samarkos, Evi Michali, John Rombos, Eleni Plata, John Meletis, Danae Abazis
Publikováno v:
Cancer genetics and cytogenetics. 86(1)
We report a man with de novo acute myeloid leukemia (M4 of the FAB classification) bearing two abnormal clones in the bone marrow cells. The clones showed trisomy 11 with loss of the Y chromosome and trisomy 13, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c13fec1a94acb1811c2222c2b7688ec3
https://pubmed.ncbi.nlm.nih.gov/8616790
https://pubmed.ncbi.nlm.nih.gov/8616790
Autor:
Anastasios Andreopoulos, John Meletis, Evi Michali, Nora Viniou, Dimitris Loukopoulos, N. Stavroyianni, G. Vaiopoulos, Xenophon Yataganas
Publikováno v:
British Journal of Haematology. 97:135-136
Trisomy 8 is the most common numerical chromosomal abnormality in myelodysplastic syndromes (MDS). Paroxysmal nocturnal haemoglobinuria (PNH) is an aquired haemolytic anaemia, clonal in nature, due to somatic mutation. PNH may evolve to aplastic anae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b0754c68edde6fd4726a65204b32ebed
https://doi.org/10.1046/j.1365-2141.1997.d01-2123.x
https://doi.org/10.1046/j.1365-2141.1997.d01-2123.x