Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Reyhan Diz-Kucukkaya"'
Autor:
Fehmi Hindilerden, Ipek Yonal-Hindilerden, Mustafa Nuri Yenerel, Meliha Nalcaci, Reyhan Diz-Kucukkaya
Publikováno v:
Hematology Reports, Vol 14, Iss 3, Pp 222-227 (2022)
No data exist for the association between the presence of accessory spleen after splenectomy and response to rituximab in immune thrombocytopenia (ITP). We investigated the relationship between accessory spleen presence and rituximab response in sple
Externí odkaz:
https://doaj.org/article/68343ad2459a4a9a8115e3b707839d6d
Publikováno v:
Annals of the rheumatic diseases. 81(7)
Zhu et al in their elegant population-based cohort study investigated the development of systemic lupus erythematosus (SLE) in patients with idiopathic (immune) thrombocytopenic purpura (ITP) and demonstrated the significantly higher risk compared wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aefe79645513be3ba695c61a98e62442
https://pubmed.ncbi.nlm.nih.gov/32988836
https://pubmed.ncbi.nlm.nih.gov/32988836
Autor:
Ipek Yonal-Hindilerden, Mustafa Nuri Yenerel, Reyhan Diz-Kucukkaya, Fehmi Hindilerden, Meliha Nalcaci
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 34, Iss 1, Pp 72-80 (2017)
Turkish Journal of Hematology, Vol 34, Iss 1, Pp 72-80 (2017)
This paper prospectively evaluates the long-term follow-up [mean ± standard deviation (SD) duration: 89.7±19.4 months] data of 15 patients (13 females and 2 males) with refractory symptomatic immune thrombocytopenia (ITP) treated with rituximab.Rit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::424e9ffc146c6f9a4bd919e59ce1b956
https://doi.org/10.4274/tjh.2016.0086
https://doi.org/10.4274/tjh.2016.0086
Autor:
Sabahattin Kaymakoglu, Reyhan Diz-Kucukkaya, Ipek Yonal, Binnur Pinarbasi, Meliha Nalcaci, Veysel Sabri Hancer, Fehmi Hindilerden
Polycythemia vera (PV), essential thrombocythemia (ET) and idiopathic myelofibrosis (IMF), collectively known as Philadelphia-negative (Ph-negative) chronic myeloproliferative neoplasms (MPNs), MPNs represent the most common causes of splanchnic vein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18781d4906bfdacbb75999b0b2d8bd91
https://hdl.handle.net/20.500.12713/574
https://hdl.handle.net/20.500.12713/574
Autor:
Michelle Remião Ugolini-Lopes, Paulo Ricardo Criado, Kurosh Parsi, Reyhan Diz Kucukkaya, Mary-Carmen Amigo, Maria G. Tektonidou, Danieli Andrade
Publikováno v:
Antiphospholipid Syndrome ISBN: 9783319554402
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dce79b1c8e35bed61cec16984c3073f7
https://doi.org/10.1007/978-3-319-55442-6_13
https://doi.org/10.1007/978-3-319-55442-6_13
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 31, Iss 4, Pp 357-362 (2014)
Turkish Journal of Hematology, Vol 31, Iss 4, Pp 357-362 (2014)
The selectins are cell adhesion molecules that mediate the interactions among leukocytes, activated platelets, and endothelial cells. We aimed to investigate whether P-selectin polymorphisms are associated with thrombosis in patients with antiphospho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::544b6bf198a00e1d9a911bca2047b9ca
https://doi.org/10.4274/tjh.2013.0091
https://doi.org/10.4274/tjh.2013.0091
Autor:
José A. López, Reyhan Diz-Kucukkaya
Publikováno v:
Hematology/Oncology Clinics of North America. 27:613-627
Platelet membrane glycoproteins play a key role in hemostasis and thrombosis. Although disorders of platelet membrane glycoproteins are rare, their effects on the lives of those affected are very important. Severe deficiencies manifest themselves ear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4bae5c3380916248fbe6bdc035ec2ca
https://doi.org/10.1016/j.hoc.2013.03.005
https://doi.org/10.1016/j.hoc.2013.03.005
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 30, Iss 1, Pp 8-12 (2013)
Turkish Journal of Hematology, Vol 30, Iss 1, Pp 8-12 (2013)
Objective: The MPL gene encodes the thrombopoietin receptor. Recently MPL mutations (MPL W515L or MPL W515K) were described in patients with essential thrombocythemia (ET) and primary (idiopathic) myelofibrosis (PMF). The prevalence and the clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aee419c9294722b2c1efafcdb1d8650b
http://europepmc.org/articles/PMC3781658
http://europepmc.org/articles/PMC3781658
Publikováno v:
Turkish Journal of Hematology
Turkish Journal of Hematology, Vol 34, Iss 4, Pp 350-351 (2017)
Turkish Journal of Hematology, Vol 34, Iss 4, Pp 350-351 (2017)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1617aa8ec9e13c9ae68b0daa40e638aa
http://europepmc.org/articles/PMC5774376
http://europepmc.org/articles/PMC5774376