Zobrazeno 1 - 10
of 138
pro vyhledávání: '"Jun Eun Park"'
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract The aim of this study is to identifying post treatment recurrence rates in pneumothorax patients under 35 and without any comorbidities according to the treatment types, gender, and age categories based on nationwide population data. Clinica
Externí odkaz:
https://doaj.org/article/3759168b56bf4cb59e19176316a43de9
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 29, Iss 1, Pp 25-29 (2022)
Ewing sarcoma is a solid tumor involving the bone and/or surrounding soft tissue, which requires multidisciplinary treatment, primarily through a combination of surgery and chemotherapy and, in some cases, radiation therapy. We present the case of a
Externí odkaz:
https://doaj.org/article/bbb12c611af24726adf56a8d8d5e50da
Publikováno v:
IEEE Access, Vol 8, Pp 171325-171333 (2020)
There has been vigorous debate on how different countries responded to the COVID-19 pandemic. To secure public safety, South Korea actively used personal information at the risk of personal privacy whereas France encouraged voluntary cooperation at t
Externí odkaz:
https://doaj.org/article/21cdbe2fdb8b4201aaea1755ad9512c0
Publikováno v:
Journal of International Medical Research, Vol 50 (2022)
Objective Children with acute lymphoblastic leukemia (ALL) may be at increased risk of psychiatric disorders. This study analyzed the incidence of psychiatric disorders in children with ALL in South Korea. Methods Using nationwide claims data for Jan
Externí odkaz:
https://doaj.org/article/94bcc666b59a441ea4f32dd7b676d8cf
Publikováno v:
Clinical Pediatric Hematology-Oncology, Vol 26, Iss 2, Pp 99-104 (2019)
Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease (RDD), is a rare histiocytic disorder of unknown etiology. Most patients with RDD have spontaneous remission, but in some patients, the disease recurs after complet
Externí odkaz:
https://doaj.org/article/f8f7e3f11458415386e1efabd8133414
Publikováno v:
Yeungnam University Journal of Medicine, Vol 36, Iss 2, Pp 148-151 (2019)
The dose of CD34+ cells is known to influence the outcome of allogeneic peripheral blood stem cell (PBSC) and/or T-cell-depleted transplantation. A previous study proposed that 2×106 CD34+ cells/kg is the ideal minimum dose for allogeneic transplant
Externí odkaz:
https://doaj.org/article/270dd3c4bc454851b76651316e4548ac
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
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 2, Pp 99-102 (2018)
Kikuchi-Fujimoto disease (KFD) is a benign and self-limited disease characterized by fever and lymphadenopathy. The etiology of KFD is unknown, but an autoimmune cause has been suggested. Hashimoto thyroiditis is the most common autoimmune thyroid di
Externí odkaz:
https://doaj.org/article/79450d7b0cc44f0eaab44df7ac71c6aa
Publikováno v:
Korean Journal of Pediatrics, Vol 59, Iss Suppl 1, Pp S92-S95 (2016)
Neuroblastomas are sometimes associated with abnormal constitutional karyotypes, but the XYY karyotype has been rarely described in neuroblastomas. Here, we report a case of an esthesioneuroblastoma in a boy with a 47, XYY karyotype. A 6-year-old boy
Externí odkaz:
https://doaj.org/article/09197dc9b54844bf9665dc7fcbf36846
Autor:
JUE SEONG LEE, JEHA KWON, HANNAH CHO, JU SUN HEO, KEE SOO HA, GI YOUNG JANG, KYU NOH, O., JUN EUN PARK
Publikováno v:
In Vivo; Jul/Aug2024, Vol. 38 Issue 4, p1984-1992, 9p