Zobrazeno 1 - 10
of 170
pro vyhledávání: '"Yoo Mi Kim"'
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 1, Pp 29-37 (2024)
Purpose The impacts of growth restriction and programming in the fetal stage on metabolic and bone health in children and adolescents are poorly understood. Moreover, there is insufficient evidence for the relationship between current growth status a
Externí odkaz:
https://doaj.org/article/8be0ce6c8e8a4acbb6d56c9bfb44d9ed
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 26, Iss 3, Pp 178-184 (2021)
Purpose The gold standard for assessing pubertal activation is the gonadotropinreleasing hormone (GnRH) stimulation test (GnRHST), which is invasive, time-consuming, and inconvenient. This study evaluated whether a single random measurement of urinar
Externí odkaz:
https://doaj.org/article/3b444efd5e08445197b375a982271de8
Autor:
Kyo Jin Jo, Yoo Mi Kim, Ju Young Yoon, Yeoun Joo Lee, Young Mi Han, Han-Wook Yoo, Hyang-Sook Kim, Chong Kun Cheon
Publikováno v:
Korean Journal of Pediatrics, Vol 62, Iss 7, Pp 274-280 (2019)
Purpose To analyze the growth response to growth hormone (GH) therapy in prepubertal patients with Noonan syndrome (NS) harboring different genetic mutations. Methods Twenty-three patients with prepubertal NS treated at Pusan National University Chil
Externí odkaz:
https://doaj.org/article/9d156438ba65450eb3cb24b44d88fda4
Publikováno v:
Chinese Medical Journal, Vol 131, Iss 1, Pp 117-118 (2018)
Externí odkaz:
https://doaj.org/article/77dee31bf2ce4f68a448dc6c19918b89
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 25, Iss 1, Pp 52-56 (2020)
Prader-Willi syndrome (PWS), an imprinting disorder, results from the loss of expression of a paternal gene on chromosome 15q11-q13. Progressive obesity and its associated complications lead to increased morbidity and early death in PWS patients. The
Externí odkaz:
https://doaj.org/article/0f5659f6031a488f98fb7ae3a632eff3
Autor:
Yoo Mi Kim
Publikováno v:
The Korean Association of General Education. 17:69-81
This paper focused on checking the concept of authorship, which is necessary in college writing class, and providing students a method on how to write in actual class. The authorship required in college writing classes is basically a characteristic r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e46cbdabe4a9cec585e88c8c477b2b3
https://doi.org/10.46392/kjge.2023.17.2.69
https://doi.org/10.46392/kjge.2023.17.2.69
Autor:
Yoo-Mi Kim
Publikováno v:
Precision and Future Medicine. 6:218-225
Children with short stature are often presented to pediatric endocrinologists. Short stature is defined as the height that is more than two standard deviations below the corresponding mean height for a specific age and sex in a reference population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::083b865b924ba26218bdd750726d0af6
https://doi.org/10.23838/pfm.2022.00142
https://doi.org/10.23838/pfm.2022.00142
Publikováno v:
Journal of Genetic Medicine. 19:105-110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f84aeb171d90f78977a5acbc5c740f2
https://doi.org/10.5734/jgm.2022.19.2.105
https://doi.org/10.5734/jgm.2022.19.2.105
Autor:
Kwanghoon Kim, Ji Young Lee, Yoo-Mi Kim, Geena Kim, Eun-Hee Kim, Byoung Kook Lee, Hyejin So, Yoowon Kwon, Jeongmin Shin, Minji Kim
Publikováno v:
Scientific Reports. 13
We retrospectively analyzed National Health Insurance claims data (January 2002–December 2018) to determine the asthma prevalence and risk factors among preterm infants born in Korea. Patients with asthma were defined as those with a history of ast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::187aa22662996c1a67c78fc3f59594aa
https://doi.org/10.1038/s41598-023-31558-z
https://doi.org/10.1038/s41598-023-31558-z
Autor:
Yoo-Mi Kim, Ja Hye Kim, Jin-Ho Choi, Gu-Hwan Kim, Jae-Min Kim, Minji Kang, In-Hee Choi, Chong Kun Cheon, Young Bae Sohn, Marco Maccarana, Han-Wook Yoo, Beom Hee Lee
Publikováno v:
Molecular Medicine, Vol 22, Iss 1, Pp 147-155 (2016)
Abstract Methionine adenosyltransferase (MAT) I/III deficiency can be Inherited as autosomal dominant (AD) or as recessive (AR) traits in which mono- or biallelic MAT1A mutations have been identified, respectively. Although most patients have benign
Externí odkaz:
https://doaj.org/article/e74cf6df38bb47809edb4041f0f50894