Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Moonbae Ahn"'
1
Akademický článek
HLA alleles, especially amino-acid signatures of HLA-DPB1, might contribute to the molecular pathogenesis of early-onset autoimmune thyroid disease.
Autor: Dong-Hwan Shin, In-Cheol Baek, Hyung Jae Kim, Eun-Jeong Choi, Moonbae Ahn, Min Ho Jung, Byung-Kyu Suh, Won Kyoung Cho, Tai-Gyu Kim
Publikováno v: PLoS ONE, Vol 14, Iss 5, p e0216941 (2019)
The major histocompatibility complex region has been suggested to play an important role in the development of autoimmune thyroid disease (AITD). In this study, we investigated the associations of human leukocyte antigen (HLA) alleles and amino acid
Externí odkaz: https://doaj.org/article/9f20d78d80fd4b35bca99154648efa73
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2
Akademický článek
Association of Polymorphisms in Toll-Like Receptors 4 and 9 with Autoimmune Thyroid Disease in Korean Pediatric Patients
Autor: Won Kyoung Cho, Jung-Pil Jang, Eun-Jeong Choi, Moonbae Ahn, Shin Hee Kim, Kyoung Soon Cho, So Hyun Park, In Cheol Baek, Min Ho Jung, Tai-Gyu Kim, Byung-Kyu Suh
Publikováno v: International Journal of Endocrinology, Vol 2017 (2017)
Background. Toll-like receptors (TLRs) have been suggested to be associated with the development of AITD. Methods. Fifteen single-nucleotide polymorphisms in 7 TLR genes were analyzed in 104 Korean children (girls = 86, boys = 18) with AITD (Hashimot
Externí odkaz: https://doaj.org/article/6f6e70911cfa456da0813cfb036787b4
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3
Discriminatory performance of insulin-like growth factor 1 and insulin-like growth factor binding protein-3 by correlating values to chronological age, bone age, and pubertal status for diagnosis of isolated growth hormone deficiency
Autor: Kyoungsoon Cho, Seulki Kim, Yoon Ji Lee, Moonbae Ahn, Byung Kyu Suh, Shin Hee Kim, Yu Jung Choi, Na Yeong Lee, Seonhwa Lee, Min Ho Jung, Won Kyoung Cho
Publikováno v: Annals of Pediatric Endocrinology & Metabolism, Vol 25, Iss 4, Pp 240-247 (2020)
Annals of Pediatric Endocrinology & Metabolism
Purpose The discriminatory performance of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor binding protein-3 (IGFBP-3) was investigated by correlating their values with chronological age (CA), bone age (BA), and pubertal status (PS
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c145fbeaa7dbeaa46911ec4167e48e40
https://doi.org/10.6065/apem.2040018.009
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4
ODP505 Polymorphisms of ITM2A rs1751094 on×Chromosome Is Associated with intractable Graves’ disease in Korean Children
Autor: Moonbae Ahn, Kyoung Soon Cho, Min Ho Jung, Byung-Kyu Suh, Sung Eun Kim, Won Kyoung Cho, Mirae Kim, In-Cheol Baek, Tai-Gyu Kim, Chungwoo Shin, Min Jeong Jang, Young Ju Choi, Na Yeong Lee, Seul K Kim, Shin Hee Kim
Publikováno v: Journal of the Endocrine Society. 6:A777-A777
Background Autoimmune thyroid diseases (AITDs) are female predominant and much attention has been focused on integral membrane protein 2A (ITM2A) on the X chromosome as Grave's disease (GD) susceptible locus. Methods We genotyped ITM2A rs1751094 sing
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c4a6be38856a7fd75938e5d761c04b5
https://doi.org/10.1210/jendso/bvac150.1605
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5
Transient Hyperinsulinemic Hypoglycemia Linked to PAX6 Mutation
Autor: Moonbae Ahn, Kyoungsoon Cho, Shin Hee Kim, Won Kyoung Cho, Jee-Min Kim, Min-Ho Jung, Byung Kyu Suh, Seulki Kim
Publikováno v: Medicina
Medicina, Vol 57, Iss 582, p 582 (2021)
Prolonged hyperinsulinemic hypoglycemia in infancy can result in developmental sequelae. A mutation in the paired box-6 gene (PAX6) has been reported to cause disorders in oculogenesis and neurogenesis. A limited number of cases of diabetes mellitus
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::012afdf407a70cf157add547d70f521c
http://europepmc.org/articles/PMC8227506
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6
Nonautoimmune congenital hyperthyroidism due to p.Asp633Glu mutation in the TSHR gene
Autor: Won Kyoung Cho, Myungshin Kim, Woori Jang, Hyojin Chae, Byung Kyu Suh, Moonbae Ahn
Publikováno v: Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 4, Pp 235-239 (2018)
Annals of Pediatric Endocrinology & Metabolism
Most cases of congenital hyperthyroidism are autoimmune forms caused by maternal thyroid stimulating antibodies. Nonautoimmune forms of congenital hyperthyroidism caused by activating mutations of the thyrotropin receptor (TSHR) gene are rare. A woma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f48c092132cd2d3f9546754958982034
https://doi.org/10.6065/apem.2018.23.4.235
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7
The effect of overweight on the luteinizing hormone level after gonadorelin stimulation test in girls with idiopathic central precocious puberty
Autor: Won Kyoung Cho, Moonbae Ahn, Byung Kyu Suh, Yoonji Lee, Hyun Young Lee
Publikováno v: Annals of Pediatric Endocrinology & Metabolism
Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 4, Pp 215-219 (2018)
Purpose We investigated the effect of overweight on luteinizing hormone (LH) levels after a gonadorelin stimulation test in Korean girls with idiopathic central precocious puberty (CPP). Methods Medical records of 234 girls diagnosed with idiopathic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62028880d385f536f5daae19ad3651f0
http://europepmc.org/articles/PMC6312921
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8
SAT-246 Insulin-Like Growth Factor-1 and Binding Protein-3 in Children with Metabolic Syndrome
Autor: Kyoungsoon Cho, Min-Ho Jung, Moonbae Ahn, Byung Kyu Suh, Seulki Kim, Yujung Choi, Won Kyoung Cho, Shin Hee Kim, Seonhwa Lee
Publikováno v: Journal of the Endocrine Society
Purpose: To examine the association of insulin-like growth factor-1 (IGF-1) and binding protein-3 (IGFBP-3) with metabolic parameters of childhood obesity and assess their relationship with the prevalence of metabolic syndrome (MetS) in childrenMetho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::249da47bde5f118551076108a6a26d34
https://doi.org/10.1210/js.2019-sat-246
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9
HLA alleles, especially amino-acid signatures of HLA-DPB1, might contribute to the molecular pathogenesis of early-onset autoimmune thyroid disease
Autor: Min Ho Jung, In-Cheol Baek, Tai-Gyu Kim, Moonbae Ahn, Hyung J. Kim, Dong-Hwan Shin, Won Kyoung Cho, Eun-Jeong Choi, Byung Kyu Suh
Publikováno v: PLoS ONE, Vol 14, Iss 5, p e0216941 (2019)
PLoS ONE
The major histocompatibility complex region has been suggested to play an important role in the development of autoimmune thyroid disease (AITD). In this study, we investigated the associations of human leukocyte antigen (HLA) alleles and amino acid
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::015a4d004e9aadb1ffc3185ba1b67632
https://doaj.org/article/9f20d78d80fd4b35bca99154648efa73
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10
Birth Weight Could Influence Bone Mineral Contents of 10- to 18-Year-Old Korean Adolescents: Results from the Korea National Health and Nutrition Examination Survey (KNHANES) 2010
Autor: Min Ho Jung, Moonbae Ahn, Yeon Jin Jeon, Kyoung Soon Cho, Won Kyoung Cho, In Ah Jung, Kyungdo Han, So Hyun Park, Shin Hee Kim, Byung Kyu Suh
Publikováno v: Hormone research in paediatrics. 85(2)
Background: We investigate the relationship between birth weight (BW) and bone mineral content (BMC) in Korean adolescents. Methods: Data were obtained from the Korea National Health and Nutrition Examination Survey conducted in 2010. Baseline charac
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a295308deed54e225883f9159392bbfc
https://pubmed.ncbi.nlm.nih.gov/26756382
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