Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pamir IŞIK"'
Autor:
Pamir IŞIK, Namık Yaşar ÖZBEK
Publikováno v:
Volume: 13, Issue: 2 57-62
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Amac: Pediatrik agir edinsel aplastik anemide eger hastanin HLA-ozdes bir aile ici donoru varsa hematopoetik kok hucre nakli ilk basamak tedavi olarak onerilmektedir. Calismada edinsel aplastik anemi tanisi ile izlenen hastalarimizin allojenik kok hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fa8dfe5d26de39accc857a3b99e46f9
https://dergipark.org.tr/tr/pub/tchd/issue/44097/539132
https://dergipark.org.tr/tr/pub/tchd/issue/44097/539132
Autor:
Zeynep Selen KARALÖK, Birce Dilge TAŞKIN, Ömer BEKTAŞ, Sevgin TANER, Pamir IŞIK, Cahide YILMAZ
Publikováno v:
Turkish Journal of Pediatric Disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90013ab70e30f02f4d6c79266226aea6
https://doi.org/10.12956/tjpd.2015.152
https://doi.org/10.12956/tjpd.2015.152
Autor:
Ayça Koca Yozgat, Ikbal Ok Bozkaya, Tekin Aksu, Pamir Isik, Mehtap Kanbur, Tugrul Tiryaki, Nese Yarali, Namik Yasar Özbek
Publikováno v:
Indian Journal of Transplantation, Vol 16, Iss 2, Pp 174-179 (2022)
Purpose: Hemorrhagic cystitis (HC) which occurs in 9%–31% of recipients after hematopoietic stem cell transplantation (HSCT) is an important cause of morbidity and mortality. Various treatment approaches have been applied for such as conservative t
Externí odkaz:
https://doaj.org/article/4774ec2133634c86a7904e96568fd5d1
Publikováno v:
Eurasian Journal of Medicine, Vol 51, Iss 1, Pp 38-41 (2019)
Externí odkaz:
https://doaj.org/article/d9baa61aea284f43987908ee492ac552
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 3, Pp 228-233 (2015)
INTRODUCTION: Venous thromboembolism (VTE) in children who undergo hematopoietic stem cell transplantation (HSCT) has high morbidity. The aim of this study is to assess the incidence of VTE in allogeneic pediatric HSCT recipients and the contribution
Externí odkaz:
https://doaj.org/article/b025ecd3ee3a4ab39f699c5b0401fd39
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 2, Pp 172-174 (2015)
Congenital amegakaryocytic thrombocytopenia (CAMT) generally begins at birth with severe thrombocytopenia and progresses to pancytopenia. It is caused by mutations in the thrombopoietin receptor gene, the myeloproliferative leukemia virus oncogene (c
Externí odkaz:
https://doaj.org/article/7ac6280e78b948fdaa4d80cbfd108a28
CANDIDA ASSOCIATED BLOODSTREAM INFECTIONS IN PEDIATRIC HEMATOLOGY PATIENTS: SINGLE CENTER EXPERIENCE
Autor:
Dilek Gurlek Gokcebay, Nese Yarali, Pamir Isik, Cengiz Bayram, Aslinur Ozkaya-Parlakay, Abdurrahman Kara, Bahattin Tunç
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 8, Iss 0, Pp e2016018-e2016018 (2016)
Background and Objectives: Candida-associated bloodstream infections are frequent and potentially life-threatening conditions in hematology patients. The aim of this study is to evaluate the characteristics, risk factors, and outcome of Candida-assoc
Externí odkaz:
https://doaj.org/article/f60577e8c3824728bd09301dd4185e1d
Autor:
Pamir Işık, Namik Özbek, Emine Dibek Mısırlıoğlu, Turan Bayhan, Suna Emir, Fatih Mehmet Azık, Bahattin Tunç
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 4, Pp 432-433 (2014)
Externí odkaz:
https://doaj.org/article/687b0ba49b894acb9bc772163b4b9c33
Autor:
Ali Fettah, Cengiz Bayram, Nese Yarali, Pamir Isik, Abdurrahman Kara, Vildan Culha, Bahattin Tunc
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 5, Iss 1, Pp e2013055-e2013055 (2013)
Introduction: The beta thalassemias are common genetic disorders in Turkey and in this retrospective study our aim was to evaluate β-globin chain mutations and the phenotypic severity of β-thalassemia patients followed-up in our hospital, a tertiar
Externí odkaz:
https://doaj.org/article/a561a7c1ea684cc9b50a8fff83fb0f5e