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Annals of Laboratory Medicine|March 14, 2013
A case of systemic mastocytosis associated with acute myeloid leukemia terminating as aleukemic mast cell leukemia after allogeneic hematopoietic stem cell transplantationMi Hyun Bae, Hyun-Ki Kim, Chan-Jeoung Park, et al.Annals of Laboratory Medicine|January 10, 2013
Activated protein C anticoagulant system dysfunction and thrombophilia in AsiaNaotaka Hamasaki, Hiroyuki Kuma, Hiroko TsudaAnnals of Laboratory Medicine|January 10, 2013
Point of care D-dimer testing in the emergency department: a bioequivalence studyShuhana Perveen, Danielle Unwin, Amith Loknath ShettyAnnals of Laboratory Medicine|January 10, 2013
Elevated levels of T helper 17 cells are associated with disease activity in patients with rheumatoid arthritisJimyung Kim, Seongwook Kang, Jinhyun Kim, et al.Annals of Laboratory Medicine|January 10, 2013
Identification of two novel NPM1 mutations in patients with acute myeloid leukemiaYongbum Jeon, Sang Won Seo, Seonyang Park, et al.Annals of Laboratory Medicine|September 5, 2013
An Increase in the clinical isolation of acquired AmpC β-lactamase-producing Klebsiella pneumoniae in Korea from 2007 to 2010Min-Jeong Park, Taek-Kyung Kim, Wonkeun Song, et al.Annals of Laboratory Medicine|July 5, 2013
Molecular epidemiology of integron-associated antimicrobial gene cassettes in the clinical isolates of Acinetobacter baumannii from northern TaiwanMing-Feng Lin, Ming-Li Liou, Chi-Chao Tu, et al.Annals of Laboratory Medicine|July 5, 2013
Comparison of the accuracy of noninvasive hemoglobin sensor (NBM-200) and portable hemoglobinometer (HemoCue) with an automated hematology analyzer (LH500) in blood donor screeningMoon Jung Kim, Quehn Park, Myung Hee Kim, et al.Annals of Laboratory Medicine|July 5, 2013
Rapid determination of chimerism status using dihydrorhodamine assay in a patient with X-linked chronic granulomatous disease following hematopoietic stem cell transplantationHyun-Young Kim, Hee-Jin Kim, Chang-Seok Ki, et al.Annals of Laboratory Medicine|July 5, 2013
A novel UMOD mutation (c.187T>C) in a Korean family with juvenile hyperuricemic nephropathyMi-Na Lee, Ji-Eun Jun, Ghee Young Kwon, et al.Pageof 101