Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ga-Young Bae"'
Autor:
Ari Song, Su Jin Kim, Min-Sun Kim, Jiyeon Kim, Insung Kim, Ga Young Bae, Eunseop Seo, Young Seok Cho, Joon Young Choi, Sung Yoon Cho, Dong-Kyu Jin
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Background/purposeGraves’ disease (GD) is the most common cause of thyrotoxicosis in children and adolescents. There is some debate regarding the optimal treatment and predicting factors of remission or relapse in children and adolescents with GD.
Externí odkaz:
https://doaj.org/article/50c9b14f435c491eba866b534645c2b1
A Korean boy with a CHD8 mutation who presented with overgrowth, intellectual disability, and autism
Autor:
Chiwoo Kim, Min-Sun Kim, Eu-seon Noh, Ga young Bae, Ja-Hyun Jang, Sae-Mi Lee, Sung Yoon Cho, Jeehun Lee, Dong-Kyu Jin
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce274e2f0f304328b57efb28aa8693be
https://doi.org/10.6065/apem.2244130.065
https://doi.org/10.6065/apem.2244130.065
Natural History and Molecular Characteristics of Korean Patients with Mucopolysaccharidosis Type III
Autor:
Min-Sun Kim, Aram Yang, Eu-seon Noh, Chiwoo Kim, Ga Young Bae, Han Hyuk Lim, Hyung-Doo Park, Sung Yoon Cho, Dong-Kyu Jin
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 5; Pages: 665
Background: Mucopolysaccharidosis type III (MPS III) is an autosomal recessive lysosomal storage disorder characterised by progressive neurocognitive deterioration. MPS III subtypes are clinically indistinguishable, with a wide range of symptoms and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e142b9ce815b6ab493237dd3f8b7a36
https://pubmed.ncbi.nlm.nih.gov/35629088
https://pubmed.ncbi.nlm.nih.gov/35629088
Autor:
Dong-Kyu Jin, Ga Young Bae, Insung Kim, Eunseop Seo, Sung Yoon Cho, Su Jin Kim, Ji-Yeon Kim, Joon Young Choi, Ari Song, Young Seok Cho, Min Sun Kim
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Frontiers in Endocrinology
Frontiers in Endocrinology
Background/purposeGraves’ disease (GD) is the most common cause of thyrotoxicosis in children and adolescents. There is some debate regarding the optimal treatment and predicting factors of remission or relapse in children and adolescents with GD.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c01343d3a66a46d595002c5d66ea41e7
https://www.frontiersin.org/articles/10.3389/fendo.2021.687834/full
https://www.frontiersin.org/articles/10.3389/fendo.2021.687834/full
Autor:
Ga Young, Bae, Min Sun, Kim, Ji-Yeon, Kim, Ja-Hyun, Jang, Sae-Mi, Lee, Sung Yoon, Cho, Dong-Kyu, Jin
Publikováno v:
Annals of clinical and laboratory science. 50(5)
Aarskog-Scott syndrome (AAS), also known as faciogenital dysplasia (FGD, OMIM # 305400), is an X-linked recessive inheritance, characterized by short stature, facial dysmorphism, and skeletal abnormalities. We report the clinical and molecular analys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::03e3bb8368e010bd81e966a0ebfade0c
https://pubmed.ncbi.nlm.nih.gov/33067218
https://pubmed.ncbi.nlm.nih.gov/33067218
Autor:
Jung Il Yoo, Jongwon Yoon, Heung Cho Ko, Woong-Ki Hong, Nam-Ho You, Seonggwang Yoo, Ga-Young Bae
Publikováno v:
Journal of Alloys and Compounds. 817:152788
Recently, deep-ultraviolet (DUV) photodetectors with useful functions including transparency and flexibility have been developed for a real-time environmental monitoring, a wearable monitoring system, transparent wireless communication, and a smart w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0bec19c710bcc3421ed73eafa1963113
https://doi.org/10.1016/j.jallcom.2019.152788
https://doi.org/10.1016/j.jallcom.2019.152788
Publikováno v:
PLoS ONE, Vol 11, Iss 1, p e0147343 (2016)
The control of radioresistance and metastatic potential of surviving cancer cells is important for improving cancer eradication by radiotheraphy. The distal-less homeobox2 (DLX2) gene encodes for a homeobox transcription factor involved in morphogene
Externí odkaz:
https://doaj.org/article/7fb54a6df5cb42f9b0e767f4d61829df