Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Chung-King Lin"'
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 30, Iss 8, Pp 409-414 (2014)
Some physicians neglect the possible coexistence of an iron deficiency with a thalassemia minor and do not treat the iron deficiency accordingly. This motivated us to conduct this study. We retrospectively reviewed the records of 3892 patients who vi
Externí odkaz:
https://doaj.org/article/d36816e223944f908d8e0a84fe596214
Publikováno v:
Kaohsiung Journal of Medical Sciences, Vol 30, Iss 8, Pp 409-414 (2014)
Some physicians neglect the possible coexistence of an iron deficiency with a thalassemia minor and do not treat the iron deficiency accordingly. This motivated us to conduct this study. We retrospectively reviewed the records of 3892 patients who vi
Autor:
Han-Ting Liu, Chung-King Lin
Publikováno v:
Journal of the Chinese Medical Association, Vol 73, Iss 7, Pp 343-352 (2010)
Testicular germ cell tumor is rare in the Asian population. Nevertheless, it is a prototypic cancer of young adults because it can be highly malignant but is also highly curable, even at an advanced stage. We present a case with far-advanced embryona
Autor:
Chung-King, Lin, Yung-Chuan, Sung
Publikováno v:
Hematology/oncology and stem cell therapy. 2(3)
Multiple myeloma is a clonal plasma cell dyscrasia with clinical heterogeneity. As of now, two key questions need to be answered before starting to treat a newly diagnosed myeloma patient. One is whether the patient is a candidate for high-dose chemo
Autor:
Mo-Ping Chow, Wen-Mei Lin, Chung-King Lin, Jaw-Lin Tzeng, Chien-Hui Yung, Hui-Yu Hu, Jeong-Shi Lin
Publikováno v:
American Journal of Hematology. 39:15-19
Lymphocytotoxicity test (LCT) and platelet suspension immunofluorescence test (PSIFT) were used together to screen platelet-associated antibodies in patients who received long-term platelet transfusion. Twenty-four of 53 patients (45.3%) were immuniz
Publikováno v:
Blood. 76:495-500
Macrophage-derived granulomonopoietic enhancing activity (GM-EA) is a novel mediator that amplifies colony formation of myeloid progenitor cells (CFU-GM) in conjunction with colony-stimulating factors (CSFs), and is distinct from other hematopoietic
Publikováno v:
Acta Haematologica. 83:137-139
Two Chinese patients with hemoglobin (Hb) H disease without a history of blood transfusion developed iron overload at the age of 45 and 53 years, respectively. Human leukocyte antigen (HLA) system types of these 2 patients were A19, A11, B13, B62 and
Autor:
Hong-Wen Peng, Elizabeth Tse, Shyh-Haw Tsay, Chien-Hui Yung, Mo-Ping Chow, Chung-King Lin, Chao-Hung Ho, Hui-Chi Hsu
Publikováno v:
American journal of hematology. 34(4)
We examined the iron status of 23 adult patients with hemoglobin H (Hb H) disease. None of them had received multiple blood transfusions or prolonged iron therapy. Studies included serum iron and ferritin concentrations, transferrin saturation, a des
Publikováno v:
The American journal of Chinese medicine. 18(3-4)
Effects of the extracts from Ganoderm lucidum (GL-P) to influence immune status of the hemophiliacs with positive HIV antibody and reversed helper/suppressor T-lymphocyte ratio were studied. Since the extracts from G. lucidum have been reported to co
Publikováno v:
American Journal of Hematology. 40:74-75