Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Erzsébet, Benedek"'
Autor:
Mariana, Tilinca1, Erzsébet, Benedek Lázár2, Beáta, Kőpeczi Judith2, Anca, Bacârea3, Claudia, Bănescu4, Benedek, I.2, Simona, Băţagă5
Publikováno v:
Acta Medica Marisiensis. Dec2011, Vol. 57 Issue 6, p776-779. 4p.
Autor:
Erzsébet Benedek, Zsuzsa Pap, Aliz-Beáta Tunyogi, Enikő Kakucs, Judit Beáta Köpeczi, I Benedek, Monica Istrati
Publikováno v:
Acta Medica Marisiensis, Vol 59, Iss 2, Pp 71-74 (2013)
Introduction: Chronic myeloid leukemia (CML) is a clonal myeloproliferative disorder; the molecular hallmark of the disease is the BCR-ABL gene rearrangement, which usually occurs as the result of a reciprocal translocation between chromosomes 9 and
Autor:
I Benedek, Monica Istrati, Enikő Kakucs, Judit Beáta Köpeczi, Aranka Kurtus, Aliz Beáta Tunyogi, Erzsébet Benedek
Publikováno v:
Acta Medica Marisiensis, Vol 59, Iss 2, Pp 111-114 (2013)
Introduction: Plasmacytoid dendritic cell leukemia is a rare subtype of acute leukemia, which has recently been established as a distinct pathologic entity that typically follows a highly aggressive clinical course in adults. The aim of this report i
Autor:
Annamária, Szántó, Zsuzsánna, Pap, Lóránd, Dénes, Erzsébet, Benedek Lázár, Adrienne, Horváth, Alíz Beáta, Tunyogi, Beáta Ágota, Baróti, Zoltán, Pávai
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 56
The Philadelphia chromosome and the resulting BCR-ABL fusion gene represent the hallmark event in chronic myeloid leukemia (CML) and their discoveries radically changed the management of these patients. Currently Wilms tumor 1 gene (WT1) is intensive
Autor:
I Benedek, Monica Istrati, Aliz-Beáta Tunyogi, Judith Beáta Köpeczi, Erzsébet Benedek, Aranka Kurtus, Enikő Kakucs
Publikováno v:
Acta Medica Marisiensis, Vol 59, Iss 3, Pp 169-171 (2013)
Introduction: Anemia is a common complication of malignant lymphomas, which could be a direct consequence of the disease or secondary to the myelosupressive chemotherapy. The aim of this study was to assess the effect of erythropoietin to treat anemi
Autor:
Judit Beáta Köpeczi, Erzsébet Benedek, I Benedek, Aliz Beáta Tunyogi, Enikő Kakucs, Monica Istrati
Publikováno v:
Acta Medica Marisiensis, Vol 59, Iss 2, Pp 91-93 (2013)
Introduction: Autologous haemopoietic stem cell transplantation (SCT) is an important treatment modality for patients with acute myeloid leukemia with low and intermediate risk disease. It has served advantages over allogenic transplantation, because
Autor:
Erzsébet, Benedek Lázár, Judit Beáta, Köpeczi, Aliz Beáta, Tunyogi, Enikő, Kakucs, Emőke, Horváth, M, Turcu, I, Benedek
Publikováno v:
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie. 54(4)
We present the possibilities of diagnosis correlating the pathological, immunophenotyping and clinical aspects of a rare case of T-cell lymphoma in a 23-year-old patient with leukemic transformation. In our consideration, it is very important to desc
Autor:
Erzsébet Benedek, Istvan Benedek, Enikő Kakucs, Aliz Beáta Tunyogi, Monica Istrati, Judit Beáta Köpeczi
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 22, Iss 1, Pp 69-77 (2014)
Neoplasmul cu celule dendritice plasmocitoide blastice (NCDPB), clasificat recent în grupul leucemiilor acute mieloide este o boală hematologică malignă rară cu evoluţie clinică extrem de agresivă. Raportăm cazul unei paciente în vârstă d
Autor:
Zoltan Bajko, Smaranda Maier, Anca Moţăţăianu, Erzsébet Benedek, Otilia Moldovan, Rodica Balasa
Publikováno v:
Romanian Journal of Laboratory Medicine, Vol 22, Iss 3, Pp 325-333 (2014)
Porfiria acută intermitentă (PAI) este o boală metabolică, cu transmitere autosomal dominantă, cu alterarea căii de biosinteză a hemului prin deficitul enzimei porphobilinogen (PBG) dezaminaza. Acest diagnostic trebuie să fie evocate în toat
Autor:
Erzsébet, Benedek Lázár1, Beáta, Köpeczi Judit1,2 kopeczijb@yahoo.com, Beáta, Tunyogi Aliz1,2, Enikő, Kakucs1,2, Alina3, Cătană3, Benedek, I.1,4
Publikováno v:
Acta Medica Marisiensis. 2013, Vol. 59 Issue 1, p49-51. 3p.