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Pediatric Hematology and Oncology|February 1, 2019
Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parentMing-Ching Shen, Ming Chen, Shung-Ping Chang, et al.
Pediatric Hematology and Oncology|December 24, 2019
Unexpected vincristine-induced systemic capillary leak syndrome in patients with Wilm's tumor: A single institution experienceYu-Tong Zhang, Lei Zhang, Yun-Ming Yao, et al.
Pediatric Hematology and Oncology|December 25, 2019
A critical ethnographic evaluation of pediatric haematology/oncology physicians and burn-outPaula Mahon
Pediatric Hematology and Oncology|December 19, 2019
Mucormycosis with peculiar aortic involvement in a child with acute lymphoblastic leukemiaGiada Biddeci, Michele Antonello, Marco Pizzi, et al.
Pediatric Hematology and Oncology|December 13, 2019
Blood product administration during high risk neuroblastoma therapyAllison Silverstein, Kiranmye Reddy, Valeria Smith, et al.
Pediatric Hematology and Oncology|March 13, 2018
Prevalence of hypertension determined by ambulatory blood pressure monitoring (ABPM) and body composition in long-term survivors of childhood cancerElif Guler, Nilgun Col, Mithat Buyukcelik, et al.
Pediatric Hematology and Oncology|June 18, 2016
Invasive Rothia infections in children with acute myeloid leukemia: A report from the Canadian infections in AML research groupJane Y Wang, Josée Brossard, Sonia Cellot, et al.
Pediatric Hematology and Oncology|February 23, 2016
Management of a Wilms' tumor with intracardiac extension using extracorporeal circulation and deep hypothermic circulatory arrest: Case report and review of the literatureBasak Erginel, Murat Ugurlucan, Murat Basaran, et al.
Pediatric Hematology and Oncology|February 23, 2016
Concentrations of adipokines in children before and after hematopoietic stem cell transplantationSzymon Skoczen, Przemyslaw J Tomasik, Kamil Fijorek, et al.
Pediatric Hematology and Oncology|December 5, 2017
Wiskott-Aldrich syndrome: Two case reports with a novel mutationKaraman Kamuran, Mecnun Çetin, Hadi Geylan, et al.
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