Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Simge Erdem"'
Autor:
Simge Erdem, Meliha Nalçacı
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 1, Pp 55-56 (2024)
Externí odkaz:
https://doaj.org/article/1c8abba7fdb845d3ae2d62ffefb33c65
Publikováno v:
İstanbul Medical Journal, Vol 24, Iss 2, Pp 204-209 (2023)
Introduction:Venous thromboembolism (VTE) is an important cause of mortality and morbidity in cancer patients. Both cancer itself and its treatment have been reported to result in an increased risk of VTE. Several scoring systems have been developed
Externí odkaz:
https://doaj.org/article/531157df21694c92b01375cadfe3f3bc
Autor:
Ulviyya Hasanzade, Yunus Catma, Nur Seda Ibılı Cetınkaya, Beyza Oluk, Simge Erdem, Cem Hacıalıoglu, Ahmet Oguz Celık, Musa Falay, Sevgi Kalayoglu Besısık
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S36- (2023)
Case report: Richter transformation may develop in lymph nodes or rarely extranodally. A 70-year-old male with an exhausted appearance had a large malodorous wound progressing to necrosis on the left chest wall. He received two treatment lines 5 year
Externí odkaz:
https://doaj.org/article/494d214dec944003af10ef2fd6bf4878
Autor:
Shirkhan Amikishiyev, Sevgi Kalayoglu Besisik, Ipek Yonal Hindilerden, Mustafa Nuri Yenerel, Arif Atahan Cagatay, Simge Erdem, Gulkan Ozkan, Meliha Nalcaci, Deniz Sargin
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S37- (2023)
Objective: This study aimed to investigate the frequency of infections after autologous hematopoietic stem cell transplantation (HSCT) in patients who were diagnosed with multiple myeloma (MM) in our tertiary center. Methodology: We conducted a singl
Externí odkaz:
https://doaj.org/article/3f147dce0f584f36b1ede9ddfea89d1a
Autor:
Tarık Onur Tiryaki, Sıdıka Gülkan Özkan, Simge Erdem, Aynur Dağlar Aday, İpek Yönal Hindilerden, Aslı Gelincik, Can Baykal, Gülçin Yegen, İbrahim Öner Doğan, Nesimi Büyükbabani, Meliha Nalçacı, Akif Selim Yavuz
Publikováno v:
BMC Cancer, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Mastocytosis is a very rare disorder and is divided into three prognostically distinct variants by World Health Organization: Cutaneous mastocytosis (CM), systemic mastocytosis (SM), and mast cell sarcoma or localized mast cell (MC) tumors.
Externí odkaz:
https://doaj.org/article/b3e0e63abb90432b9167a0783d6e5362
Autor:
Murat Özbalak, Metban Mastanzade, Dilek Özden Özlük, Tarık Onur Tiryaki, Simge Erdem, Ezgi Pınar Özbalak, Tuğrul Elverdi, İpek Yçnal Hindilerden, Ali Yılmaz Altay, Gülçin Yeğen, Ahmet Emre Eşkazan, Muhlis Cem Ar, Mustafa Nuri Yenerel, Teoman Soysal, Meliha Nalçacı, Burhan Ferhanoğlu, Sevgi Kalayoğlu Beşışık
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 4, Pp 254-261 (2022)
Objective: Redditux® (RED), as a biosimilar rituximab, was approved in Turkey for all indications of the original Mabthera® (MAB) in March 2018. The aim of our study was to evaluate the efficacy and safety of RED in de novo diffuse large B-cell lym
Externí odkaz:
https://doaj.org/article/2a9fff72faa5467abb4cb2fad80cdfb5
Autor:
Hilal Konyaoglu, Ali Yilmaz Altay, Emine Göknur Işik, Beyza Oluk, Nigar Taghiyeva, Elif Sakci, Simge Erdem, Gülçin Yeğen, İpek Yönal Hindilerden, Mustafa Nuri Yenerel, Meliha Nalcaci, Sevgi Kalayoglu Besisik
Publikováno v:
HemaSphere, Vol 7, p e09840e4 (2023)
Externí odkaz:
https://doaj.org/article/8681a538aca2453e8063d447cb685277
Publikováno v:
Turkish Journal of Hematology, Vol 39, Iss 3, Pp 215-217 (2022)
Externí odkaz:
https://doaj.org/article/af982ce5c9444520a3cbae42dfc86e38
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S19- (2022)
Objective: Erdheim Chester disease (ECD) is a rare non-Langerhans histiocytic multisystem disorder. ECD is most commonly manifested as multifocal sclerotic long bone lesions. Orbital and intraocular manifestations are rare. We report an unusual bilat
Externí odkaz:
https://doaj.org/article/15207114f69c4ec2b5cf9df6cdb7c409
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S19- (2022)
Objective: Involvement of the lung is common in systemic AL amyloidosis in post-mortem series. However, the diagnosis is challenging. Histology is the gold standard but may result in bleeding. Consequently, diagnosis during life is rare. Case report:
Externí odkaz:
https://doaj.org/article/8865ad5fc29d4eb3b5477d604f058021