Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Sifa Sahın"'
Autor:
Deniz Tugcu, Leyla Valıyeva, Sifa Sahın, Rumeysa Tuna, Mustafa Bılıcı, Ayşegül Unuvar, Serap Karaman, Gülşah Tanyıldız, Selda Hancerli, Sevim Mese, Ali Agacfıdan, Ayper Somer, Zeynep Karakas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S29- (2023)
Objective: Respiratory viruses are an important cause of morbidity and mortality in pediatric hematology oncology patients. We aimed to determine the infection rate, clinical and epidemiological characteristics of respiratory viruses in pediatric pat
Externí odkaz:
https://doaj.org/article/a5ac561e39a84f96a97da1c4a21f9fff
Autor:
Melda Berber Hamamcı, Şule Yeşil, Firdevs Aydın, Gülcan Erbaş, Deniz Tuğcu, Şifa Şahin, Zuhal Bayramoğlu, Yasin Ateş, Serap Karaman, Hikmet Gülşah Yıldız, Hakan Kocaman, Elif Dede, Ayper Somer, Ayşegül Ünüvar, Zeynep Karakaş
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S46-S47 (2023)
Case report: The 22-month-old male and 15-day-old female patients presented with persistent stridor since birth. Tracheoscopy of the first patient revealed a 90% obstructing hemangioma in the subglottic area, while the second patient's CT scan showed
Externí odkaz:
https://doaj.org/article/a72efa10807e48008a63c0fe551f4dc2
Autor:
Şifa Şahin, Serap Karaman, Yasin Yılmaz, Mustafa Bilici, Saadet Aslan, Hikmet Gülşah Tanyıldız, Deniz Tuğcu, Zeynep Karakaş, Ayşegül Ünüvar
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S21-S22 (2022)
Objective: It is known that there were transportation problems to the hospital and treatment experienced in many disease groups during the pandemic process. The negative impact of the pandemic is particularly evident in chronic diseases and in situat
Externí odkaz:
https://doaj.org/article/303e82360c2a4b31a26bbff631e8ec50
Autor:
Serap Karaman, Şifa Şahin, Edibe Pembegül Yıldız, Hikmet Gülşah Tanyıldız, Mehmet Barburoğlu, Tutku Turgut, Yasin Yılmaz, Zeynep Karakaş, Deniz Tuğcu, Ayşegül Ünüvar
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S43- (2022)
Introduction: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder. NF-1 vasculopathy is a significant complication of the disease. It affects both arterial and venous blood vessels of all sizes. Also Moyamoya syn
Externí odkaz:
https://doaj.org/article/b07cf4caf4d54ed5be7db4a2086bdcb2
Autor:
Aysegul Unuvar, Levent Aydemir, Mehmet Barburoglu, Sifa Sahin, Mustafa Bilici, Deniz Tugcu, Gulsah Tanyildiz, Zeynep Karakas, Serap Karaman
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss , Pp S38- (2022)
Objective: The bleeding phenotype of patients with inherited FVII deficiency is variable, and epistaxis is one of the most frequent symptoms. Interestingly, the bleeding risk does not correlate with the level of FVII activity. The severity of FVII de
Externí odkaz:
https://doaj.org/article/053327ea2a074902baa51921d11d0d93
Autor:
Mustafa Bilici, Serap Karaman, Aysegul Unuvar, Deniz Tugcu, Gülsah Tanyildiz, Ayca Dilruba Aslanger, Oya Uyguner, Rumeysa Tuna Deveci, Sifa Sahin, Zeynep Karakas
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S62-S63 (2021)
Objective: Polycythemia is a rare condition in which an increase in erythrocyte mass is observed. It can be primary or secondary. Primary polycythemia occurs as a result of congenital or acquired mutations that regulate erythroid development. Althoug
Externí odkaz:
https://doaj.org/article/09a147323fc14bf7894b83150b43b840
Autor:
Serap Karaman, Mustafa Bilici, Ayşegül Ünüvar, Deniz Tuğcu, Gülşah Tanyıldız, Rumeysa Tuna Deveci, Gülçin Yegen, Şifa Şahin, Zeynep Karakaş
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss , Pp S60-S61 (2021)
Objective: Chronic myeloid leukemia (CML) is rarely seen in children. The development of myelofibrosis in CML is not uncommon and is associated with a poor prognosis. In cases unresponsive to treatment, tyrosine kinase mutation should be checked for
Externí odkaz:
https://doaj.org/article/a1adf842c03041b58f9bd8dd0082a76e