Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vildan Culha"'
Autor:
Tahir Atik, Esra Işık, Hüseyin Onay, Bilçağ Akgün, Moharram Shamsali, Kaan Kavaklo, Melike Evim, Gülen Tüysüz, Namık Yaşar Özbek, Fahri Şahin, Zafer Salcıoğlu, Canan Albayrak, Yeşim Oymak, Ekrem Ünal, Fatma Burcu Belen, Ebru Yılmaz Keskin, Can Balkan, Birol Baytan, Alphan Küpesiz, Vildan Culha, Tuba Nur Tahtakesen, Adalet Meral Güneş, Ferda Özkınay
Publikováno v:
Turkish Journal of Hematology, Vol 37, Iss 3, Pp 145-153 (2020)
Objective: Hemophilia A (HA) is the most severe X-linked inherited bleeding disorder caused by hemizygous mutations in the factor 8 (F8) gene. The aim of this study is to determine the mutation spectrum of the F8 gene in a large HA cohort from Turkey
Externí odkaz:
https://doaj.org/article/739b1796010f4465a28442c9b6243a1b
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
Autor:
Şerife Öztekin Güntaş, Volkan Köse, Ayça Koca Yozgat, Vildan Çulha, Namık Yaşar Özbek, Aslınur Parlakay, Neşe Yaralı
Publikováno v:
The Journal of Pediatric Academy, Vol 4, Iss 4, Pp 122-127 (2023)
Infections are a significant cause of morbidity and mortality of chemotherapy-induced neutropenia in children with acute leukemia. The aim of this study was to evaluate microbiologically documented infections (MDIs) during febrile neutropenia (FN) ep
Externí odkaz:
https://doaj.org/article/b7123f08ea8b43fe9a86a277dee4b33e
Publikováno v:
Journal of back and musculoskeletal rehabilitation. 27(3)
BACKGROUNDS AND OBJECTIVES: Hemophilic arthropathy due to recurrent joint bleeding leads to physical, psychological and socioeconomic problems in children with hemophilia and reduces their quality of life. The purpose of this study was to evaluate jo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98fd035ef5549fdd2280236fc2731943
https://pubmed.ncbi.nlm.nih.gov/24346152
https://pubmed.ncbi.nlm.nih.gov/24346152
Autor:
Gökcen MERAL, Volkan KÖSE, Vildan ÇULHA, AYÇA KOCA YOZGATLI, NAMIK YAŞAR ÖZBEK, HÜSNİYE NEŞE YARALI
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S55- (2021)
Objective: This cross-sectional study aimed to reveal possible hemostatic disorders in patients referred to the Pediatric Hematology Department due to the prolongation of the prothrombin test (PT) or activated partial thromboplastin test (aPTT). Meth
Externí odkaz:
https://doaj.org/article/d9230d001a464e47a6d1e36aa2667d7f
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S56-S57 (2021)
Case report: Immune thrombocytopenia (ITP) is the most common platelet disorder in children, peaking between the ages of 1-7.The first line therapy consists of intravenous immunoglobulin, anti-D immunoglobulin or corticosteroids. Second-line treatmen
Externí odkaz:
https://doaj.org/article/e532f33be60f441e91ddee70a06808f3
Publikováno v:
Turkish Journal of Hematology, Vol 34, Iss 2, Pp 183-183 (2017)
Externí odkaz:
https://doaj.org/article/236f59cfc68d40108dbf08bef332a2d7