Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Eirini, Kouroupi"'
Autor:
Axel Rüfer, Hubert Angermann, Rudolf Benz, Nicolas Bonadies, Antonello Calderoni, Nathan Cantoni, Anna Efthymiou, Robert Escher, Geneviève Favre, Dorothea Friess, Andreas Gschwend, Andreas Himmelmann, Andreas Holbro, Peter Keller, Eirini Kouroupi, Thomas Lehmann, Nikolaus Pedarnig, Véronique Rigamonti, Kaveh Samii, Adrian Schmidt, Hans-Peter Schäfer, Roland Sperb, Georg Stüssi, Annette Winkler, Reinhard Zenhäusern, Jeroen S. Goede, on behalf of the SLIM-Registry Investigators
Publikováno v:
HemaSphere, Vol 6, Iss 7, p e741 (2022)
Externí odkaz:
https://doaj.org/article/96e57933677a4445bcd61d39ea571d5b
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
Autor:
Emmanuel E. Douzinas, Christina Piperi, George Creatsas, Ekaterini Koulouri, Anastasios Kalofoutis, Evanthia Diamanti-Kandarakis, Krystallenia I Alexandraki, Eirini Kouroupi, Stefanos Lazaridis, Helen A. Kandarakis, Nikolaos Katsilambros, Joanna Papailiou
Publikováno v:
Metabolism. 55:494-500
Exogenous advanced glycation endproducts (AGEs, known atherogenic molecules) abundant in everyday precooked, rich in fat, overheated meals can possibly contribute to the increased risk for diabetes and cardiovascular disease in women with polycystic
Autor:
J J Kiladjian, Christine Dosquet, Nadine Bonnin, Bruno Cassinat, Lionel Adès, Christine Chomienne, M L Menot, Eirini Kouroupi, William Vainchenker
Publikováno v:
Blood Cancer Journal
The detection of the JAK2V617F mutation has become an essential tool in BCR-ABL1-negative myeloproliferative neoplasms (MPNs) diagnosis, as it is present in 95% of polycythemia vera (PV) patients and 60% of essential thrombocytemia (ET) or myelofibro
Autor:
Eirini Kouroupi, Antoine F. Carpentier, Pierre Fenaux, Segolene Billot, Caroline Jardin, Thierry Laperche, Johan Le Guilloux, Bruno Cassinat, Jean-Jacques Kiladjian
Patients with essential thrombocythemia often complain of various subjective neurological symptoms. This prospective study aims to assess their incidence and response to therapy. Among 37 consecutive patients with essential thrombocythemia, 11 presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282675ea51db9cd9caf4c0850ebfef90
https://europepmc.org/articles/PMC3232271/
https://europepmc.org/articles/PMC3232271/
Autor:
Eirini, Kouroupi, Katerina, Zoi, Nathalie, Parquet, Christine, Zoi, Jean-Jacques, Kiladjian, Vassiliki, Grigoraki, William, Vainchenker, Franck, Lellouche, Christophe, Marzac, Marie-Hélène, Schlageter, Christine, Dosquet, Linda M, Scott, Pierre, Fenaux, Dimitris, Loukopoulos, Christine, Chomienne, Bruno, Cassinat
Publikováno v:
British journal of haematology. 142(4)
Autor:
Dominique Valla, Bruno Cassinat, Sylvia Bellucci, Eirini Kouroupi, Jean-Jacques Kiladjian, Christine Chomienne, Christine Dosquet
Publikováno v:
Blood. 117:5777-5778
To the editor: We read with interest the recently published report by Smalberg et al, which describes the frequency of the JAK2 46/1 haplotype among patients with splanchnic vein thrombosis (SVT).[1][1] Indeed, recent studies revealed that the 46/1 h
Autor:
Eirini Kouroupi, Bernard Granchamp, Dominique Valla, Bruno Cassinat, Christine Chomienne, Jean-Jacques Kiladjian, Sylvia Bellucci, Aurélie Plessier
Publikováno v:
Blood. 116:4120-4120
Abstract 4120 Aim: The majority of myeloproliferative neoplasms (MPN), i.e. Polycythemia vera (PV), Essential Thrombocytemia (ET) and Primary Myelofibrosis, are characterized by the presence of the acquired JAK2V617F gene mutation. Recent studies rev
Autor:
Eirini Kouroupi, Nathalie Parquet, Christine Zoi, Linda M. Scott, Bruno Cassinat, Christine Chomienne, Katerina Zoi, Vassiliki Grigoraki, Jean-Jacques Kiladjian, Pierre Fenaux, Dimitris Loukopoulos, Christine Dosquet
Publikováno v:
Blood. 110:2534-2534
Since the description in 2005 of the recurrent V617F JAK2 gene mutation in MPD patients, we have tested more than 1500 patients each year and confirmed the relative frequency of this mutation in distinct MPD subclasses and its usefulness in classyfyi