Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Surekha Tony"'
Publikováno v:
HemaSphere, Vol 7, p e26367bb (2023)
Externí odkaz:
https://doaj.org/article/97c2ff0eb3e64bb9bfb029b83068aa4e
Publikováno v:
HemaSphere, Vol 7, p e69507c9 (2023)
Externí odkaz:
https://doaj.org/article/bb6497b18f71460ea9cfc76ff72b3803
Publikováno v:
Pediatric Hematology and Oncology. 39:48-61
BACKGROUND Rare coagulation disorders represent 3-5% of all inherited coagulation deficiencies and are usually inherited as autosomal recessive. Oman has high rate of consanguineous marriages; we aimed to study the prevalence, presentation and manage
Publikováno v:
Cardiology in the young. 31(3)
Anthracycline-related cardiomyopathy is of concern in children treated for acute myeloid leukemia (AML). Risk is dose-dependent, increasing with higher doses. We aim to highlight the risk of early-onset cardiotoxicity with low-cumulative anthracyclin
Autor:
Doaa Khater, Rashid Al Abri, Mohamed Elshinawy, Nada Al Marhoobi, Yasser Wali, Surekha Tony Mevada, Islam Elghamry, Hanan F. Nazir, Abdulhakim Al-Rawas, Manar Maktoom
Publikováno v:
Transfusion. 60
Background Many children with sickle cell disease (SCD) indicated for adenotonsillectomy receive pre-operative transfusion therapy, either simple or exchange transfusion, in order to reduce surgical and sickle cell disease-related complications. Subj
Autor:
Mohamed Elshinawy, Abdul H. Al-Rawas, Shahina Daar, Surekha Tony Mevada, Mathew Zachariah, Yasser Wali, Najma Al-Mahruqi, Ismail El-Beshlawi
Publikováno v:
Sultan Qaboos University Medical Journal, Vol 16, Iss 1, Pp 78-81 (2016)
Magnetic resonance imaging using T2* (MRI T2*) is a highly sensitive and non-invasive technique for the detection of tissue iron load. Although the single breath-hold multi-echo T2* technique has been available at the Sultan Qaboos University Hospita
Autor:
Shahina Daar, Hamoud Al-Dhuhli, Khalid Al-Rasadi, Surekha Tony Mevada, Nasser Al-Kemyani, Murtadha Al-Khabori, Sunil Bhandari
Publikováno v:
Hemoglobin. 38:365-368
Historically, renal involvement has not been a commonly recognized complication in patients with β-thalassemia major (β-TM). Herein, we studied the impact of iron overload on glomerular filtration rate (GFR) estimated by cystatin C based GFR (Cyst
Autor:
Yasser Wali, Salam Alkindi, Yasser Mahfouz, Iman Al Fadhali, Surekha Tony Mevada, Murtadha Al-Khabori, Asma Al Shezawi, Farah Al-Kindy, Naema Al-Shibli, Abdulhakim Al Rawas
Publikováno v:
Blood. 134:3577-3577
Background: Sickle cell disease is a common hemaglopinapthy worldwide and in Oman. Avascular necrosis (AVN) of the hip causes significant morbidity to patients with sickle cell disease and has a profound impact on their quality of life. This study ai
Autor:
Mathew Zachariah, Wafa Bashir, Surekha Tony, Yasser Wali, Ismail El-Beshlawi, Abdulhakim Al-Rawas, Mohamed Elshinawy
Publikováno v:
Pediatric Hematology and Oncology. 31:442-447
The role of erythropoiesis-stimulating agents (ESAs) in the management of chemotherapy-induced anemia (CIA) is becoming increasingly recognized in the field of medical oncology, with paucity of data in pediatrics. We evaluated the efficacy and tolera
Publikováno v:
Journal of pediatric hematology/oncology. 38(5)
To improve treatment outcome in young patients with homozygous β-thalassemia, evaluation of factors associated with health-related quality of life (HRQoL) is essential to develop clinical, counseling, social, and school support programs. This study