Zobrazeno 1 - 10
of 91
pro vyhledávání: '"Yi-Kong Keung"'
Autor:
Eddie H. Hu, Yi-Kong Keung
Publikováno v:
Journal of Oncology Pharmacy Practice. 25:1261-1264
We report an unusual case of spontaneous intramuscular hematoma associated with antiproteinase 3 antibody in a patient with metastatic squamous cell carcinoma receiving nivolumab and the medical literature is reviewed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58ab3fde45522221c32ed8eb73b091b9
https://doi.org/10.1177/1078155218786352
https://doi.org/10.1177/1078155218786352
Publikováno v:
Journal of Oncology Pharmacy Practice. 25:234-238
5-fluorouracil and capecitabine are chemotherapeutic agents commonly used to treat solid malignancies. Increased susceptibility to 5-fluorouracil or capecitabine, caused by impaired clearance, dihydropyrimidine dehydrogenase deficiency, or other gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43ac5ffca952b6f7d2bed9cc16bf5131
https://doi.org/10.1177/1078155217732141
https://doi.org/10.1177/1078155217732141
Publikováno v:
Journal of oncology pharmacy practice : official publication of the International Society of Oncology Pharmacy Practitioners. 26(1)
We report a case of acute myeloid leukemia with complex cytogenetic abnormalities suggestive of preexisting myelodysplastic syndrome in a patient with habitual ingestion of colloidal silver as nutritional supplement for over 10 years and the medical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db527c9fd1ede0dc9e3305716ab666a9
https://pubmed.ncbi.nlm.nih.gov/30854923
https://pubmed.ncbi.nlm.nih.gov/30854923
Publikováno v:
Journal of Oncology Pharmacy Practice. 22:548-551
Pharmacogenetics is a study of how genetic variation of an individual affects the drug response. We report a case of recurrent pancytopenia resulting from maintenance chemotherapy in a patient with acute promyelocytic leukemia and two pharmacogenetic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4605a8cfe703d6d1cc58e6639f35de99
https://doi.org/10.1177/1078155215577235
https://doi.org/10.1177/1078155215577235
Autor:
Yi-Kong Keung, John Owen
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis. 10:387-391
Compared to primary thrombocytosis such as that caused by essential thrombocytosis, reactive thrombocytosis is generally regarded as benign. However, reactive thrombocytosis has infrequently been reported to cause severe and even fatal complications.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47f54876fe30d8c5664e62b97bdb1c67
https://doi.org/10.1177/107602960401000412
https://doi.org/10.1177/107602960401000412
Autor:
Bayard L. Powell, David H. Buss, Istvan Molnar, Yi-Kong Keung, Michael W. Beaty, Mark J. Pettenati
Publikováno v:
Leukemia Research. 28:579-586
We conducted a retrospective study to define the significance of Philadelphia chromosome (Ph) in myelodysplastic syndrome and acute leukemia in the adults at this institution and the literature was reviewed. One hundred forty-eight cases of t(9;22)(q
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d216de992d07db9ff9af4d0b734e7058
https://doi.org/10.1016/j.leukres.2003.10.027
https://doi.org/10.1016/j.leukres.2003.10.027
Publikováno v:
Cancer Genetics and Cytogenetics. 139:9-13
Klinefelter syndrome was first described in 1942 as an endocrine disorder characterized by gynecomastia, hypogonadism, small testes, and elevated levels of follicle-stimulating hormone. An extra X chromosome (i.e., 47,XXY) was subsequently demonstrat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::609c9565c8f31b24d9b88b5c9e342324
https://doi.org/10.1016/s0165-4608(02)00626-x
https://doi.org/10.1016/s0165-4608(02)00626-x
Publikováno v:
Cancer Genetics and Cytogenetics. 136:78-81
Chromosomal anomalies involving region 3q21q26 have been reported associated with thrombocytosis in various hematological malignancies, such as chronic myeloid leukemia, myelodysplastic syndrome, and acute myeloid leukemia (AML). Recent reports descr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038634986d9c76f92955b15783f5b0bd
https://doi.org/10.1016/s0165-4608(02)00521-6
https://doi.org/10.1016/s0165-4608(02)00521-6
Autor:
Bayard L. Powell, Mark J. Pettenati, David H. Buss, Julia M. Cruz, Ralph D. Woodruff, Yi-Kong Keung
Publikováno v:
American Journal of Hematology. 66:167-171
Cytogenetic abnormalities in association with aplastic anemia have been reported fairly infrequently. Clonal cytogenetic abnormalities at initial diagnosis are uncommon. A retrospective study was performed of the cytogenetic findings in patients with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba1c78e73374297755f0b9eb95c6b963
https://doi.org/10.1002/1096-8652(200103)66:3<167::aid-ajh1040>3.0.co
https://doi.org/10.1002/1096-8652(200103)66:3<167::aid-ajh1040>3.0.co
Publikováno v:
The Journal of the American Board of Family Medicine. 13:76-79
Porphyrias are a group of metabolic disorders, usually genetic in origin, secondary to deficiencies of various enzymes involved in the heme biosynthetic pathways. They are usually classified into hepatic and erythropoietic types based on the major si
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b686488bee81d9bda6c05e8c0e9a22b7
https://doi.org/10.3122/jabfm.13.1.76
https://doi.org/10.3122/jabfm.13.1.76