Zobrazeno 1 - 10
of 347
pro vyhledávání: '"Keon-Hee Yoo"'
Autor:
Ju-Yong Song, Jae-Suh Park, Joo-Hwan Kim, Joon-Ho Wang, Holly C. Heck, Bruce E. Heck, Dong-Hyun Kim, Keon-Hee Yoo
Publikováno v:
Cells, Vol 11, Iss 19, p 2934 (2022)
Osteoarthritis (OA) is a chronic degenerative joint disease accompanied by an inflammatory milieu that results in painful joints. The pathogenesis of OA is multifactorial, with genetic predisposition, environmental factors, and traumatic injury resul
Externí odkaz:
https://doaj.org/article/08270eb952a54f159b511486a6aac354
Autor:
Hoi Soo Yoon, Hee-Jin Kim, Keon-Hee Yoo, Ki-Woong Sung, Hong-Hoe Koo, Hyoung Jin Kang, Hee Young Shin, Hyo Seop Ahn, Ji-Yoon Kim, Young-Tak Lim, Keun-Wook Bae, Ki-O Lee, Ji-Sook Shin, Seung-Tae Lee, Hae-Sun Chung, Sun-Hee Kim, Chan-Jeoung Park, Hyun-Sook Chi, Ho-Joon Im, Jong Jin Seo
Publikováno v:
Haematologica, Vol 95, Iss 4 (2010)
Background Familial hemophagocytic lymphohistiocytosis is a fatal disease characterized by immune dysregulation from defective function of cytotoxic lymphocytes. Three causative genes have been identified for this autosomal recessive disorder (PRF1,
Externí odkaz:
https://doaj.org/article/644623faa5ee4dbb8e3e7e918e15446e
Autor:
Hyungsuk Jin, Ji Won Lee, Hee Young Ju, Hee Won Cho, Ju Kyung Hyun, Ki Woong Sung, Hong Hoe Koo, Hee-Jin Kim, Keon Hee Yoo
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 27, Iss 2, Pp 120-123 (2020)
Hereditary spherocytosis (HS) is the most common inherited red cell membrane disorder. Its main laboratory finding is anemia with reticulocytosis. However, in the case of an aplastic crisis, there may be no reticulocytosis, making the diagnosis of HS
Externí odkaz:
https://doaj.org/article/ef2d719eff8f4036a9f9a4a7fca45ef5
Autor:
Won Kyung Kwon, Jee Ah Kim, Jong-Ho Park, Doo Ri Kim, Su Eun Park, Yae Jean Kim, Keon Hee Yoo, Ja-Hyun Jang, Eun Suk Kang
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
X-linked lymphoproliferative disease type 1 (XLP1), an X-linked recessive genetic disorder, is associated with primary immunodeficiency. Patients with XLP1 are susceptible to Epstein–Barr virus (EBV) infection. SH2D1A gene is known as the causative
Externí odkaz:
https://doaj.org/article/ad08c6141b274b5fa132ad899acc930b
Autor:
Yoomi Park, Hyery Kim, Heewon Seo, Jung Yoon Choi, Youngeun Ma, Sunmin Yun, Byung-Joo Min, Myung-Eui Seo, Keon Hee Yoo, Hyoung Jin Kang, Ho Joon Im, Ju Han Kim
Publikováno v:
Journal of Translational Medicine, Vol 18, Iss 1, Pp 1-13 (2020)
Abstract Background NUDT15 and TPMT variants are strong genetic determinants of thiopurine-induced hematological toxicity that results in therapeutic failure in pediatric acute lymphoblastic leukemia (ALL). However, many patients with both wild-type
Externí odkaz:
https://doaj.org/article/b2dcb0a3832a43a88b9fad6b99480b16
Autor:
Hyoung Soo Choi, Qute Choi, Jung-Ah Kim, Kyong Ok Im, Si Nae Park, Yoomi Park, Hee Young Shin, Hyoung Jin Kang, Hoon Kook, Seon Young Kim, Soo-Jeong Kim, Inho Kim, Ji Yoon Kim, Hawk Kim, Kyung Duk Park, Kyung Bae Park, Meerim Park, Sang Kyu Park, Eun Sil Park, Jeong-A Park, Jun Eun Park, Ji Kyoung Park, Hee Jo Baek, Jeong Ho Seo, Ye Jee Shim, Hyo Seop Ahn, Keon Hee Yoo, Hoi Soo Yoon, Young-Woong Won, Kun Soo Lee, Kwang Chul Lee, Mee Jeong Lee, Sun Ah. Lee, Jun Ah Lee, Jae Min Lee, Jae Hee Lee, Ji Won Lee, Young Tak Lim, Hyun Joo Jung, Hee Won Chueh, Eun Jin Choi, Hye Lim Jung, Ju Han Kim, Dong Soon Lee, The Hereditary Hemolytic Anemia Working Party of the Korean Society of Hematology
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)
Abstract Background Current diagnostic tests for hereditary spherocytosis (HS) focus on the detection of hemolysis or indirectly assessing defects of membrane protein, whereas direct methods to detect protein defects are complicated and difficult to
Externí odkaz:
https://doaj.org/article/abee68d56a8e4cec884160b107e54fd9
Autor:
Young Bae Choi1, Keon Hee Yoo2,3,4 hema2170@skku.edu
Publikováno v:
Cancer Research & Treatment. Apr2022, Vol. 54 Issue 2, p572-578. 7p.
Autor:
Eunsang Suh, Sunghwan Shin, Hee Young Ju, Keon Hee Yoo, Hyun-Young Kim, Duck Cho, Sun-Hee Kim, Hee-Jin Kim
Publikováno v:
Annals of Laboratory Medicine. 43:204-207
Autor:
Kyung Mi Park1, Keon Hee Yoo2, Seong Koo Kim3, Jae Wook Lee3, Nack-Gyun Chung3, Hee Young Ju2, Hong Hoe Koo2, Chuhl Joo Lyu4, Seung Min Han4, Jung Woo Han4, Jung Yoon Choi5, Kyung Taek Hong5, Hyoung Jin Kang5, Hee Young Shin5, Ho Joon Im6, Kyung-Nam Koh6, Hyery Kim6, Hoon Kook7, Hee Jo Baek7, Bo Ram Kim7
Publikováno v:
Cancer Research & Treatment. Jan2022, Vol. 54 Issue 1, p269-276. 8p.
Publikováno v:
Korean Journal of Pediatrics, Vol 61, Iss 2, Pp 53-58 (2018)
PurposeAlthough the prognosis is generally good in patients with intermediate-risk neuroblastoma, no consensus has been reached on the ideal treatment regimen. This study analyzed treatment outcomes and toxicities in patients younger than 18 months w
Externí odkaz:
https://doaj.org/article/bc6b32945b234f9cb3a01602010bbe8a