Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Canbolat Ayhan A"'
Autor:
Bülent Zülfikar, Başak Koç, Fahri Şahin, Hatice İlgen Şaşmaz, Kaan Kavaklı, Can Balkan, Ali Bülent Antmen, Sinan Akbayram, Birol Güvenç, Vahap Okan, Emine Türkkan, Canan Albayrak, Davut Albayrak, Nazan Sarper, Tülin Tiraje Celkan, Orhan Ayyıldız, Salih Aksu, Türkan Patıroğlu, Zafer Şalcıoğlu, Adalet Meral Güneş, Yasemin Altuner Torun, Ümran Çalışkan, Hüseyin Tokgöz, Yılmaz Ay, Gül Nihal Özdemir, Mehmet Sönmez, Ekrem Ünal, Ahmet Fayik Öner, Nil Güler, Osman Alphan Küpesiz, Hale Ören, Serap Karaman, Ayşegül Ünüvar, Mehmet Dağlı, Ahmet Muzaffer Demir, Murat Söker, Bülent Alioğlu, Zühre Kaya, Aylin Canbolat Ayhan, Zafer Bıçakçı, Yusuf Ziya Aral, Muhlis Cem Ar
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 8, Iss 7, Pp 102588- (2024)
Background: Hemophilia B (HB), an X-linked recessive inherited bleeding disorder, exhibits a high prevalence among males. Objectives: To present the first national cohort of persons with HB to define the demographics, clinical characteristics, and tr
Externí odkaz:
https://doaj.org/article/a0df4776626d4dedb5af1ad41e8bc5f5
Autor:
Zeynep Reyhan Onay, Yetkin Ayhan, Sinem Can Oksay, Deniz Mavi, Aysenur Toksoz Yıldırım, Aylin Canbolat Ayhan, Saniye Girit
Publikováno v:
Thoracic Research and Practice, Vol 24, Iss 1, Pp 49-52 (2023)
Externí odkaz:
https://doaj.org/article/638f34b957994687bae2d35b68c1099e
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S23- (2021)
Objective: Children with thalassemia major are prone to growth failure and micronutrient deficiency. In this study, we aimed to evaluate nutritional status, anthropometrics, bone mineralization defects in regularly transfused patients. Methodology: W
Externí odkaz:
https://doaj.org/article/f8f193168b6e4e2ca35eb74974b224c4
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S24-S25 (2021)
Objective: In this study, we aimed to investigate the nutritional status after treatment in pediatric patients who have completed treatment with the diagnosis of acute lymphoblastic leukemia. Methodology: We analyzed the data obtained by evaluating p
Externí odkaz:
https://doaj.org/article/75a809208c8745a9ab487d220c62bfcc
Autor:
Ayşegül Ünüvar, Serap Karaman, Deniz Tuğcu, Melike Sezgin Evim, Arzu Akçay, İbrahim Eker, Funda Tayfun Küpesiz, Namık Özbek, Mehmet Ertem, Sultan Aydın, Zuhal Keskin, Yusuf Ziya Aral, Zülfükar Gördü, Murat Elli, Ayşe Özkan Karagenç, Burcu Belen Apak, Hülya Uzel, Murat Söker, Tuba Karapınar, Yeşim Oymak, Nihal Karadaş, Alper Özcan, Ersin Töret, Ülker Koçak, Sinan Akbayram, Şule Ünal Cangül, Aylin Canbolat Ayhan, Tiraje Celkan, Bülent Zülfikar, Rejin Kebudi, Şadan Hacısalihoğlu, Erol Erduran, Sema Aylan Gelen, Nazan Sarper, Fatih Erbey, Emin Kürekçi, Hüseyin Gülen, Barış Yılmaz, Ömer Doğru, Ahmet Koç, Selma Ünal, Hüseyin Tokgöz, Canan Albayrak, Yılmaz Ay, Fatih Orhan, Davut Albayrak, Neslihan Karakurt, Betül Orhaner, Emine Türkkan, Yıldız Yıldırmak, Hadi Geylani, Begüm Koç, Ahmet Fayik Öner, Çetin Timur, Hale Ören
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S55-S56 (2021)
Objective: A questionnaire form was prepared by the Turkish Pediatric Hematology Society- Subcommittee of Hemostasis, Thrombosis and Hemophilia to determine the current approaches in the diagnosis and treatment of childhood ITP in our country. Our ai
Externí odkaz:
https://doaj.org/article/0eb80f230816404ab892c71ef0fed017
Autor:
Zeliha Guzelkucuk, Deniz Yılmaz Karapınar, Sema Aylan Gelen, Huseyin Tokgoz, Alper Ozcan, Yılmaz Ay, Aysenur Bahadır, Namik Yasar Ozbek, Ayse Ceyda Oren, Aylin Canbolat Ayhan, Arzu Akyay, Burcu Akıncı, Nihal Karadas, Aysegul Unuvar, Hale Oren, Ali Fettah, Zuhre Kaya, Bilgen Isık, İbrahim Eker, Serap Karaman, Aysen Turedi Yıldırım, Mehmet Fatih Orhan, Yesim Oymak, Cetin Timur, Nalan Yazici, Ayse Simsek, Neslihan Karakurt, Ersin Toret, Melike Sezgin Evim
Background: In patients with acute lymphoblastic leukemia (ALL), the risk of thromboembolism increases due to hemostatic changes secondary to the primary disease and due to treatment-related factors. In this multicenter study, we aimed to research th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::120b9f448b2357ebc3be82c8438e5a7b
https://avesis.deu.edu.tr/publication/details/25ff087a-08e0-48ca-aaa8-6acf9baa6f73/oai
https://avesis.deu.edu.tr/publication/details/25ff087a-08e0-48ca-aaa8-6acf9baa6f73/oai
Autor:
BULGURCU, Serap Cevher1, CANBOLAT AYHAN, Aylin2 canbolataylin@hotmail.com, EMEKSIZ, Hamdi Cihan3, OVALI, Fahri1
Publikováno v:
Medeniyet Medical Journal. 2021, Vol. 36 Issue 4, p325-332. 8p.
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S23-(2021)
Medeniyet Medical Journal, Vol 36, Iss 4, Pp 325-332 (2021)
Medeniyet Medical Journal
Medeniyet Medical Journal, Vol 36, Iss 4, Pp 325-332 (2021)
Medeniyet Medical Journal
Children with thalassemia major (TM) are prone to growth failure and micronutrient deficiency. Thus, this study aimed to evaluate nutritional status, anthropometrics, and bone mineralization defects in patients with regular blood transfusion.Data obt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22929e94358d3077a24a0a48171ff62b
https://doi.org/10.4274/mmj.galenos.2021.66915
https://doi.org/10.4274/mmj.galenos.2021.66915
Publikováno v:
Gazzetta Medica Italiana Archivio per le Scienze Mediche. 181
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f6e83e42c47e6424373989ae8fe45a08
https://doi.org/10.23736/s0393-3660.21.04715-x
https://doi.org/10.23736/s0393-3660.21.04715-x
Autor:
ÖZCAN, ALPER, Bulduk, Tuba, KARATAŞ, AYŞE, Sengoz, Ceyda Ozcelik, ÇAĞLIYAN, GÜLSÜM AKGÜN, Kucukdiler, Ayse Hilal Eroglu, Celkan, Tiraje, AKDENİZ, AYDAN, GÜVEN, ZEYNEP TUĞBA, Kis, Cem, Ipek, Yildiz, Ekinci, Omer, Maral, Senem, Karakus, Sema, ÇENELİ, ÖZCAN, PAYDAŞ, SEMRA, Kucukyurt, Selin, ELVERDİ, TUĞRUL, CANDAR, ÖMER, ÖZKALEMKAŞ, FAHİR, ÖZKOCAMAN, VİLDAN, KARAMAN GÜLSARAN, SEDANUR, Umit, Elif Gulsum, KIRKIZLAR, HAKKI ONUR, GÜNDÜZ, EREN, ÖREN, HALE, Ozdemir, Gul Nihal, Ozturk, Sule Mine Bakanay, TÖRET, ERSİN, KARTAL, İBRAHİM, CANBOLAT AYHAN, AYLİN, Apak, Fatma Burcu Belen
Castleman disease (CD) is a rare disease also known as angiofollicular lymph node hyperplasia. The two main histological subtypes are the hyaline vascular and plasma cell variants. It is further classified as unicentric CD (UCD) or multicentric CD (M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1355213137d9a3af624c19cb8a3db66
https://avesis.deu.edu.tr/publication/details/c06ffedc-d6b2-4d2c-9f3f-50f856e787e1/oai
https://avesis.deu.edu.tr/publication/details/c06ffedc-d6b2-4d2c-9f3f-50f856e787e1/oai