Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Fatma Keklik, Karadag"'
Autor:
Esma Evrim Dogan, Aysenur Arslan, Naciye Demirel, Demet Aydin, Ilknur Mansuroglu, Suheyla Atak, Fatma Keklik Karadag, Rafet Eren, Guray Saydam
Publikováno v:
Bulletin of the National Research Centre, Vol 46, Iss 1, Pp 1-14 (2022)
Abstract Background Multiple myeloma (MM) is characterized by infiltration of neoplastic plasma cells in the bone marrow. Although many novel agents have been developed in the last decade, MM remains a non-curable disease. The association between bon
Externí odkaz:
https://doaj.org/article/86604a17b20f42c089ac157e51eb16bf
Autor:
Karla Cavazos, Sheila Eswaran, Cathleen Maidlow, Fatma Keklik Karadag, Ramazan Idilman, Ilkay Idilman, Ira Miller, Jamile Shammo, Nancy Reau, Celalettin Ustun
Publikováno v:
Blood Advances. 6:5630-5633
[No Abstract Available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2817b30178ef2e52b9f93a375df8b7b0
https://doi.org/10.1182/bloodadvances.2022008038
https://doi.org/10.1182/bloodadvances.2022008038
Autor:
Fahir Özkalemkaş, Omer Ekinci, Elif Birtas Atesoglu, Güray Saydam, Mustafa Merter, Elif Gülsüm Ümit, İbrahim Ethem Pinar, Ufuk Demirci, Unal Atas, Merih Reis Aras, Meltem Ayli, Bengü Çöbanoğlu Şimşek, Volkan Baş, Ferda Can, Sedanur Karaman Gulsaran, Fulya Oz Puyan, Mustafa Albayrak, Vildan Gürsoy, Semra Paydas, Murat Yıldırım, Olga Meltem Akay, Selcuk Korkmaz, Özgür Mehtap, Berrin Balık Aydın, Leylagür Kaynar, Ozan Salim, Imdat Dilek, Zeynep Tuğba Güven, Meltem Kurt Yuksel, Huseyin Saffet Bekoz, Fatma Keklik Karadag, Mesut Ayer, Ahmet Demir, Hakki Onur Kirkizlar, Erman Öztürk
Background: Diffuse large B-cell lymphoma (DLBCL) is the most common sub-type of Non-Hodgkin lymphomas (NHL) and it is a very heterogeneous group of diseases. CD5 positivity is profound in a substantial patient population in DLBCL. In this population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5fe55f39d858ca81f1c51b582ab612e
https://doi.org/10.21203/rs.3.rs-987276/v1
https://doi.org/10.21203/rs.3.rs-987276/v1
Autor:
Celalettin Ustun, Smarika Sapkota, Jo Anne H. Young, Qing Cao, Daniel J. Weisdorf, Steven Richmond, Karam M. Obeid, Timothy L. Pruett, Allison P Watson, Fatma Keklik Karadag
Publikováno v:
Transplant infectious disease : an official journal of the Transplantation SocietyREFERENCES. 24(1)
Background Clostridioides difficile infection (CDI) frequently complicates allogeneic hematopoietic stem cell (allo-HCT) and solid organ transplantation (SOT). Methods We retrospectively analyzed risk factors and outcomes of CDI occurring within 30 d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df5c254ba509b978b5d790d9176f3ce8
https://pubmed.ncbi.nlm.nih.gov/34455662
https://pubmed.ncbi.nlm.nih.gov/34455662
Autor:
Fatma Keklik, Karadag, Mustafa Nuri, Yenerel, Mehmet, Yılmaz, Hava, Uskudar, Vildan, Ozkocaman, Tülin Firatli, Tuglular, Fuat, Erdem, Ali, Unal, Orhan, Ayyildiz, Gülsüm, Ozet, Melda, Comert, Emin, Kaya, Mesut, Ayer, Ozan, Salim, Birol, Guvenc, Hakan, Ozdogu, Özgur, Mehtap, Mehmet, Sonmez, Nil, Guler, Sibel, Hacioglu, İsmet, Aydogdu, Ozlen, Bektas, Selami Kocak, Toprak, Lale, Kaynar, Munci, Yagci, Salih, Aksu, Anil, Tombak, Volkan, Karakus, İrfan, Yavasoglu, Birgul, Onec, Mehmet Ali, Ozcan, Levent, Undar, Rıdvan, Ali, Osman, Ilhan, Guray, Saydam, Fahri, Sahin
Publikováno v:
Am J Blood Res
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare X-linked genetic disorder. On the contrary to its name, it is a multisystemic disease and various symptoms other than hemoglobinuria could be occurred. It could be life threatening especially becaus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::76544d69a9a4a4548ccbd6ae58f4fdae
https://pubmed.ncbi.nlm.nih.gov/34322292
https://pubmed.ncbi.nlm.nih.gov/34322292
The goal of complete remission (CR) in acute leukemias could be achieved with intensive induction chemotherapy however patients need post remission consolidation strategies such as high-dose chemotherapy, or autologous (ASCT) or allogeneic (allo-SCT)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67f8a6934dda60dd817f84774836726d
https://doi.org/10.5772/intechopen.94424
https://doi.org/10.5772/intechopen.94424
Autor:
Fatma Keklik Karadag, Sait Şen, Banu Sarsik, Huseyin Toz, Mehmet Ozkahya, Gulay Asci, Güray Saydam, Aygul Celtik
Background: Kidney involvement is a common manifestation that contributes to morbidity and mortality in systemic amyloidosis. Amyloid load can be predicted by histopathological grading of amyloid deposits in kidney biopsy specimens. Our aim was to de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d2e44cbd3cd479f9cfa420694bd49a3b
https://doi.org/10.21203/rs.3.rs-194799/v1
https://doi.org/10.21203/rs.3.rs-194799/v1
Publikováno v:
European Medical Journal Hematology (2020)
Paroxysmal nocturnal haemoglobinuria (PNH) is a rare, nonmalignant, haematopoietic clonal disorder that manifests with haemolytic anaemia, thrombosis, and peripheral blood cytopenias. The diagnosis is based on laboratory findings of intravascular hae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85b2e88b11b798ffa138a8170f63afbf
https://www.emjreviews.com/hematology/article/is-allogeneic-stem-cell-transplantation-a-good-option-for-paroxysmal-nocturnal-haemoglobinuria/
https://www.emjreviews.com/hematology/article/is-allogeneic-stem-cell-transplantation-a-good-option-for-paroxysmal-nocturnal-haemoglobinuria/
Autor:
Meltem Sezis Demirci, Cenk Gokalp, Matthias C. Braunisch, Mahmut Töbü, Fatma Keklik Karadag, Celalettin Ustun, Mehmet Ozkahya, Hatice Demet Kiper, Christoph Schmaderer, Emrah Gunay
Introduction Platelet dysfunction is not uncommon in patients with end-stage renal disease (ESRD). Type of renal replacement therapy may have an effect on platelet functions, which has not been well investigated. We evaluated in vitro closure time (C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1499225fb6597758fca0d27459030a1
https://hdl.handle.net/11454/70183
https://hdl.handle.net/11454/70183
Autor:
Mehmet Ali Özcan, Orhan Ayyildiz, Celalettin Ustun, Rıdvan Ali, Birgül Öneç, Emin Kaya, Güray Saydam, Ismet Aydogdu, Nil Güler, Mesut Ayer, Anil Tombak, Hakan Ozdogu, Yılmaz Mehmet, Vildan Ozkocaman, Ozlen Bektas, Hava Üsküdar Teke, Salih Aksu, Ali Ünal, Fatma Keklik Karadag, Özgür Mehtap, Fuat Erdem, Ozan Salim, Fahri Şahin, Osman Ilhan, Sibel Hacioglu, Gülsüm Özet, Levent Undar, Birol Guvenc, Irfan Yavasoglu, Tulin Firatli Tuglular, Volkan Karakuş, Münci Yağcı, Selami Kocak Toprak, Lale Aydın Kaynar, Melda Cömert Özkan, Mehmet Sönmez, Mustafa Nuri Yenerel
61st Annual Meeting and Exposition of the American-Society-of-Hematology (ASH) -- DEC 07-10, 2019 -- Orlando, FL
Onec, Birgul/0000-0003-2824-1044; OZDOGU, HAKAN/0000-0002-8902-1283
WOS:000577164604216
[No Abstract Available]
Amer
Onec, Birgul/0000-0003-2824-1044; OZDOGU, HAKAN/0000-0002-8902-1283
WOS:000577164604216
[No Abstract Available]
Amer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f366027d86b2d64784d06ed0c39a2800
https://hdl.handle.net/20.500.12684/10987
https://hdl.handle.net/20.500.12684/10987