Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hyoun-Ah Kim"'
Autor:
Kyung Eun Lee, In Ah Choi, Ju-Yang Jung, Ha Rim Yeon, Hyoun-Ah Kim, Nga Thi Trinh, Hyun Jeong Kim, Joohee Kim, Woorim Kim
Publikováno v:
Pharmacogenetics and Genomics. 32:10-15
Objectives Nuclear factor of activated T cells C2 (NFATC2) is known as a member of the transcription family and enhances tumor necrosis factor-alpha (TNF-α) synthesis in human T cells at the gene transcription level. Although NFATC2 has a potential
Publikováno v:
Medicine. 101:e28908
Systemic lupus erythematosus (SLE) is an autoimmune disease of unknown etiology with diverse clinical and laboratory manifestations, including thrombocytopenia. About 25% of patients with SLE may be affected by thrombocytopenia, many of whom are asym
Publikováno v:
Medicine. 100:e26843
INTRODUCTION Secondary amyloidosis is a rare complication of rheumatoid arthritis (RA) that is histologically characterized by the deposition of amyloid fibrils in target organs, such as the kidneys and gastrointestinal tract. Controlling the inflamm
Publikováno v:
Medicine
MEDICINE(96): 45
MEDICINE(96): 45
Rheumatoid arthritis (RA) is a risk factor for bone fragility, and its effect on fracture risk is independent of bone mineral density (BMD). The trabecular bone score (TBS) is a new indirect parameter of bone quality. In this study, BMD and the TBS w
Autor:
Chang Hee Suh, Hyoun-Ah Kim, Moon Seung Soh, Yoo Jin Um, Jin Hee Jung, Young Hwan Ahn, Ju-Yang Jung
Publikováno v:
Medicine. 95:e2818
The aim of the study was to examine the clinical characteristics and prognosis according to severity of thrombocytopenia and response to treatment for thrombocytopenia in patients with systemic lupus erythematosus (SLE).We retrospectively evaluated 2
Publikováno v:
Medicine
Adult-onset Still disease (AOSD) is characterized by fever, skin rash, and lymphadenopathy with leukocytosis and anemia as common laboratory findings. We investigated the characteristic pathologic findings of skin, lymph node, liver, and bone marrow
Publikováno v:
Medicine. 94:e451
Hemophagocytic syndrome (HPS) is a potentially life-threatening complication of systemic inflammatory disorders. Adult-onset Still disease (AOSD) is one of the systemic autoimmune diseases associated with reactive hemophagocytic syndrome (RHS). This
Publikováno v:
JCR: Journal of Clinical Rheumatology. 15:40-41