Výsledky vyhledávání - "Wafaa Abdelghany"

Congenital protein C deficiency with renal vein thrombosis and central retinal venous occlusion in a term neonate due to novel mutation in the PROC gene

Autor: Hussain Parappil, Mahmoud Oklah, Anant Pai, Wafaa Abdelghany, Hilal Al Rifai, Abubakr Imam

Publikováno v: Journal of Clinical Neonatology. 6:116

Severe protein C (PC) deficiency is a rare disorder caused by homozygous or compound heterozygous genetic anomalies. PC deficiency is inherited as autosomal dominant, and most patients are heterozygous for a genetic defect. Homozygous or compound het

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::96d99c2954aeec43825ebb59523cd9a2
https://doi.org/10.4103/jcn.jcn_111_16

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Multiple Packed Red Blood Cell (PRBC) Transfusions In Pediatric Patients With Acute Myeloid Leukemia (AML) Result In a Large Transfusional Iron Dose With The Potential For Long-Term Organ Dysfunction

Autor: Suleiman Al-Sweedan, Asim F. Belgaumi, Neameh Farhan, Ali Al-Ahmari, Amal Al-Seraihy, Mohammed Al-Darwish, Wafaa Abdelghany, Hassan El-Solh

Publikováno v: Blood. 122:2660-2660

The treatment of AML in children utilizes intensive chemotherapy and often myeloablative hematopoietic cell transplant (HCT). This results in significant myelosuppression, necessitating blood product transfusions. Repeated PRBC transfusions result in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0db563b7743ad5afe2f934de58adceca
https://doi.org/10.1182/blood.v122.21.2660.2660

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