Zobrazeno 1 - 10
of 644
pro vyhledávání: '"H Losonczy"'
Publikováno v:
Gynecologic and Obstetric Investigation. 61:111-114
Inherited thrombophilias are associated with an increased risk of maternal thromboembolism and certain adverse pregnancy outcomes, including second- and third-trimester fetal loss, placental abruption, severe intrauterine growth restriction, and earl
Autor:
Cappelletti, Martina1 (AUTHOR) m.cappelletti@uniroma1.it, Pallotta, Lucia1 (AUTHOR) lucia.pallotta@uniroma1.it, Vona, Rosa2 (AUTHOR) rosa.vona@iss.it, Tinari, Antonella2 (AUTHOR) antonella.tinari@iss.it, Pisano, Annalinda3 (AUTHOR) annalinda.pisano@uniroma1.it, Casella, Giovanni4 (AUTHOR) giovanni.casella@uniroma1.it, Crocetti, Daniele4 (AUTHOR) daniele.crocetti@uniroma1.it, Carlomagno, Dominga1 (AUTHOR) dominga.carlomagno@uniroma1.it, Tattoli, Ivan1 (AUTHOR) ivan.tattoli70@gmail.com, Giordano, Carla3 (AUTHOR) carla.giordano@uniroma1.it, Matarrese, Paola2 (AUTHOR) paola.matarrese@iss.it, Severi, Carola1 (AUTHOR) carola.severi@uniroma1.it
Publikováno v:
International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 17, p9680. 14p.
Publikováno v:
Zeitschrift für Gastroenterologie. 46
Publikováno v:
35th Hemophilia Symposium ISBN: 3540285431
Hepatic veno-occlusive disease (VOD) is a common complication following hematopoietic stem cell transplantation (HSCT), it is reported to occur in 5–70% of patients undergoing HSCT. The different incidence of VOD between series may be related to th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a693b7385aa47591783ac35a2302d849
https://doi.org/10.1007/3-540-28546-6_53
https://doi.org/10.1007/3-540-28546-6_53
Autor:
H. Losonczy, M. Dávid
Publikováno v:
Fibrinolysis. 8:31-33
In this study a strong negative correlation was found between ECLT (citrated plasma) and t-PA activity (Stabilyte plasma) and a weak positive correlation between ECLT and PAI-1 activity in healthy volunteers before venous occlusion. Two groups of vol
Autor:
M, Kecskés, A, Nagy, T, Vidra, G, Kispál, G, Radványi, K, Vezendi, L, Hajnal, R, Kellner, H, Losonczy
Publikováno v:
Orvosi hetilap. 142(7)
The authors report the first data having applied the indirect genomic diagnosis in carrier screening in Hungary. 22 patients with haemophilia B and female family members of 14 out of them were examined by PCR based restriction fragment length polymor
Autor:
B, Gasztonyi, A, Pár, A, Szomor, A, Nagy, L, Kereskai, H, Losonczy, L, Pajor, M, Horanyi, G, Mózsik
Publikováno v:
Orvosi hetilap. 141(49)
Oncogenesis is a multifactorial process in which environmental, genetical and infectious factors may be of importance. Specific viruses are supposed to have etiological role in about 15% of human tumors. Recently the B-cell proliferation inducing eff
Publikováno v:
30th Hemophilia Symposium Hamburg 1999 ISBN: 9783540676775
Hemophilia B (factor IX deficiency) is an X-linked inherited bleeding disorder of blood coagulation. Hungary belongs to the Caucasians with its 10 million citizens. According to current statistics 179 patients with hemophilia B have been registered.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7b2bae7fb40303bff4dfcd64022933b
https://doi.org/10.1007/978-3-642-18240-2_39
https://doi.org/10.1007/978-3-642-18240-2_39
[The role of TNF-alpha in myelodysplastic syndrome: immunoserologic and immunohistochemical studies]
Publikováno v:
Orvosi hetilap. 141(33)
TNF alpha is a highly active cytokine which plays an important role in the regulation of apoptotic cell death, a mechanism involved in the pathophysiology of myelodysplastic syndrome (MDS). In this study we investigated the expression of TNF alpha on
Autor:
A, Matolcsy, Z, Borbényi, J, Demeter, M, Egyed, S, Fekete, J, Földi, L, Gergely, P, Kajtár, G, Kelényi, A, Kiss, T, László, D, Lehoczky, H, Losonczy, M, Nagy, K, Pál, K, Pálóczy, G, Radványi, I, Semsei, G, Varga, M, Udvardy
Publikováno v:
Orvosi hetilap. 141(25)
In B-cell non-Hodgkin's lymphomas (NHL), clonal rearrangement of the immunoglobulin heavy chain (IgH) gene provides a useful marker for the detection of minimal residual disease (MRD) after treatment. To explore clinical usefulness of polymerase chai