Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Dimitris, Loukopoulos"'
Autor:
Dimitris Loukopoulos
Publikováno v:
Thalassemia Reports, Vol 4, Iss 3 (2014)
The inherited hemoglobin disorders are a challenging topic for many reasons; they are caused by a variety of interesting molecular mechanisms, have a complicated pathophysiology, they constitute a multifaceted medical problem with pain and misery for
Externí odkaz:
https://doaj.org/article/02ab33e5862244f890c2afcf962fb27f
Autor:
Michael Angastiniotis, Androulla Eleftheriou, Eleni Antoniou, Dimitris Loukopoulos, Angelo Loris Brunetta, Eva Maria Knoll, Lily Cannon, Anton Skafi, George Constantinou
Publikováno v:
Thalassemia Reports; Volume 11; Issue 1; Pages: 9803
Hemoglobin disorders (thalassemia and sickle cell disease) are a group of hereditary anemias that today occur across the world. The recent population movement has led to a steady increase of carriers and patients in all countries of the European Unio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3efd3560c83ba040cf40dab655a20542
Autor:
Dimitris Loukopoulos
Publikováno v:
Thalassemia Reports, Vol 3, Iss 1s, Pp e2-e2 (2013)
Thalassemia is a disease with many challenging aspects. It is caused by a variety of interesting molecular mechanisms, has a complicated pathophysiology, constitutes a multifaceted medical problem with pain and misery for the patients and unhappiness
Externí odkaz:
https://doaj.org/article/95a5a60acef5417fb071f192d9e4ee60
Autor:
Dimitris Loukopoulos
Publikováno v:
Thalassemia Reports, Vol 3, Iss 1s, Pp e14-e14 (2013)
The inherited hemoglobin disorders not only cause suffering and unhappiness to the patients but they also absorb a large part of resources and human effort in several countries which harbor the deleterious genes. Numbers are frightening! Africa, with
Externí odkaz:
https://doaj.org/article/6089e6c0a13c4c3daba655c40129abc6
Autor:
J. Christakis, G.S. Lucas, Ronald L. Nagel, K De Ceulaer, Graham R. Serjeant, A.J. Bellingham, H.H. Billett, Dimitris Loukopoulos, John Stuart
Publikováno v:
Clinical Hemorheology and Microcirculation. 10:35-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ace401ba40397109cf4ca2235b38a2e8
https://doi.org/10.3233/ch-1990-10104
https://doi.org/10.3233/ch-1990-10104
Autor:
Angeliki Balassopoulou, Evangelia-Eleni Delaki, Veroniki Komninaka, Dimitris Loukopoulos, Maria N. Dimopoulou, Effrossyni Boutou, Ersi Voskaridou, Dimitrios Christoulas, Evangelos Terpos
Publikováno v:
European Journal of Haematology. 93:492-499
Objective Progress in the management of patients with thalassemia intermedia (TI) enabled increasing rates of pregnancies among TI women worldwide. Nevertheless, information regarding TI pregnancy management and outcome is quite limited in the litera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::319a51ac5e122414dc3a1ab1244b8854
https://doi.org/10.1111/ejh.12387
https://doi.org/10.1111/ejh.12387
Autor:
Dimitris Loukopoulos, Maria Dalekou, Effie Apostolidou, Christos Meletis, Michalis Samarkos, Konstantinos Korovesis, Evangelos Terpos, John Meletis, Veroniki Komninaka, Eleni Variami, Efstathios Paravasiliou, Konstantinos Konstantopoulos, Olga Benopoulou
Publikováno v:
Hematology (Amsterdam, Netherlands). 5(6)
During bone marrow engraftment following BMT there is a re-establishment of fetal erythropoiesis, expressed by the increase of F-cells. This seems to depend on several factors such as underlying disease, conditioning before therapy and other mechanis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d24d96321f67152b2e55ba6855793951
https://pubmed.ncbi.nlm.nih.gov/27419348
https://pubmed.ncbi.nlm.nih.gov/27419348
Autor:
Evangelos Terpos, Konstantinos Varvagiannis, Dimitris Loukopoulos, George Stamatopoulos, Ersi Voskaridou, Eleni Plata, Antonios Bilalis, Dimitrios Christoulas, Klio Sinopoulou, Aggeliki Balassopoulou
Publikováno v:
Blood. 115:2354-2363
The aim of this prospective study was to evaluate the long-term efficacy and safety of hydroxyurea (HU) in patients with sickle cell disease (SCD). Thirty-four patients with sickle cell anemia (hemoglobin S [HbS]/HbS), 131 with HbS/β0-thal, and 165
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::580414055a7d4b688ff91505aad61881
https://doi.org/10.1182/blood-2009-05-221333
https://doi.org/10.1182/blood-2009-05-221333
Autor:
Ch. Sakellariou, Dimitris Loukopoulos, A.K. Stamulakatou, N.P. Laoutaris, S.V. Alexia, George Paterakis, G.N. Terzoglou, I.G. Papassotiriou, Evangelos Premetis, P.V. Siourounis
Publikováno v:
Clinical & Laboratory Haematology. 16:235-245
Summary. Shape changes of abnormally deformed red cells in aperture impedance haematology analysers are known to affect MCV, MCHC and haematocrit estimation. However, different counters vary in the manifestation of this effect. We performed a compara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::552f62e8140d74b3dbfffbbc18ef9872
https://doi.org/10.1111/j.1365-2257.1994.tb00416.x
https://doi.org/10.1111/j.1365-2257.1994.tb00416.x
Autor:
Vassiliki Grigoraki, Franck Lellouche, Christine Dosquet, Christine Chomienne, Dimitris Loukopoulos, Bruno Cassinat, Nathalie Parquet, Katerina Zoi, Christophe Marzac, Marie-Hélène Schlageter, William Vainchenker, Christine Zoi, Jean-Jacques Kiladjian, Linda M. Scott, Eirini Kouroupi, Pierre Fenaux
Publikováno v:
British Journal of Haematology. 142:676-679
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca1b7e92b02c74551115c793b192527d
https://doi.org/10.1111/j.1365-2141.2008.07223.x
https://doi.org/10.1111/j.1365-2141.2008.07223.x