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European Journal of Haematology|June 18, 2014
Clinical features, genetics, and outcome of pediatric patients with hemophagocytic lymphohistiocytosis in Korea: report of a nationwide survey from Korea Histiocytosis Working PartyKyung-Nam Koh, Ho Joon Im, Nak-Gyun Chung, et al.Annals of Laboratory Medicine|May 12, 2025
Chromosomal Rearrangements in 1,787 Cases of Acute Leukemia in Korea over 15 yearsDongGeun Son, Ho Cheol Jang, Young Eun Lee, et al.Sensors (Basel, Switzerland)|December 11, 2025
Novel Wearable-Based Real-Time Temperature Monitoring in Hospitals for Febrile Adverse Events in Patients with Cancer: A Prospective Feasibility StudyYun Kwan Kim, Seo-Yeon Ahn, Sun Jung Lee, et al.Journal of Korean Medical Science|May 4, 2010
Efficacy of tandem high-dose chemotherapy and autologous stem cell rescue in patients over 1 year of age with stage 4 neuroblastoma: the Korean Society of Pediatric Hematology-Oncology experience over 6 years (2000-2005)Ki Woong Sung, Hyo Seop Ahn, Bin Cho, et al.Pediatric Transplantation|February 2, 2010
The outcome of hematopoietic stem cell transplantation in Korean children with hemophagocytic lymphohistiocytosisHoi Soo Yoon, Ho Joon Im, Hyung Nam Moon, et al.Journal of Korean Medical Science|August 2, 2016
Characteristics and Outcomes of Second Malignant Neoplasms after Childhood Cancer Treatment: Multi-Center Retrospective SurveyKyung-Nam Koh, Keon Hee Yoo, Ho Joon Im, et al.Haematologica|July 29, 2010
Weekly rituximab followed by monthly rituximab treatment for steroid-refractory chronic graft-versus-host disease: results from a prospective, multicenter, phase II studySeok Jin Kim, Jong Wook Lee, Chul Won Jung, et al.Journal of Korean Medical Science|April 15, 2003
Autologous stem cell transplantation for the treatment of neuroblastoma in KoreaKyung Ha Ryu, Hyo Seop Ahn, Hong Hoe Koo, et al.Human Mutation|April 14, 2025
Genome Sequencing of Rare Disease Patients Through the Korean Regional Rare Disease Diagnostic Support ProgramRin Khang, Hane Lee, Jihye Kim, et al.Medicine|July 21, 2017
Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotypeJin-Ho Choi, Beom Hee Lee, Sun Hee Heo, et al.Pageof 13