Zobrazeno 1 - 10
of 101
pro vyhledávání: '"Cheol Woo Ko"'
Autor:
Yun Jeong Lee, Yunha Choi, Han-Wook Yoo, Young Ah Lee, Choong Ho Shin, Han Saem Choi, Ho-Seong Kim, Jae Hyun Kim, Jung Eun Moon, Cheol Woo Ko, Moon Bae Ahn, Byung-Kyu Suh, Jin-Ho Choi
Publikováno v:
Endocrinology and Metabolism, Vol 37, Iss 2, Pp 359-368 (2022)
Background Discontinuing growth hormone (GH) treatment during the transition to adulthood has been associated with adverse health outcomes in patients with childhood-onset growth hormone deficiency (CO-GHD). This study investigated the metabolic chan
Externí odkaz:
https://doaj.org/article/e1e487b3084747b38e4baf71d5322918
Publikováno v:
Journal of Yeungnam Medical Science, Vol 39, Iss 1, Pp 46-52 (2022)
Background The coronavirus disease 2019 (COVID-19) outbreak in the Daegu-Gyeongbuk area in 2020 has caused difficulties in the daily life and hospital care of children with type 1 diabetes mellitus (T1DM). We detected an increase in blood sugar level
Externí odkaz:
https://doaj.org/article/9065c2ac6e234e17bced1d55c3e30773
Autor:
Jinsup Kim, Min-Sun Kim, Byung-Kyu Suh, Cheol Woo Ko, Kee-Hyoung Lee, Han-Wook Yoo, Choong Ho Shin, Jin Soon Hwang, Ho-Seong Kim, Woo Yeong Chung, Chan Jong Kim, Heon-Seok Han, Dong-Kyu Jin
Publikováno v:
BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background Short stature is the most consistent characteristic feature of Turner syndrome (TS). To improve final heights of children with TS effectively, it is important to provide them with early and appropriate treatment using growth hormo
Externí odkaz:
https://doaj.org/article/500ec73b48574b1495f48871491ae936
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 26, Iss 1, Pp 24-30 (2021)
Purpose Autosomal dominant hypocalcemia with hypercalciuria is a genetic disease characterized by hypoparathyroidism with hypercalciuria. We discovered a novel variant (p.Tyr825Phe[Y825F]) of the CASR gene in a neonate with congenital hypoparathyroid
Externí odkaz:
https://doaj.org/article/53ad1ff1165c4cfab047798c1916e261
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 25, Iss 2, Pp 132-136 (2020)
Alport syndrome (AS) is a rare genetic disorder that causes progressive nephritis and is more common among males. Studies have reported an association between thyroid antibodies and hypothyroidism in patients with AS, but the relevance of this relati
Externí odkaz:
https://doaj.org/article/39c3d5c458cd4a78a38e573810064964
Autor:
Yena Lee, Jin-Ho Choi, Arum Oh, Gu-Hwan Kim, Sook-Hyun Park, Jung Eun Moon, Cheol Woo Ko, Chong-Kun Cheon, Han-Wook Yoo
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 25, Iss 2, Pp 97-103 (2020)
Purpose Cytochrome P450 oxidoreductase (POR) deficiency is a rare autosomal recessive disorder caused by mutations in the POR gene encoding an electron donor for all microsomal P450 enzymes. It is characterized by adrenal insufficiency, ambiguous gen
Externí odkaz:
https://doaj.org/article/1322a94709504038b2d82a505f95cafc
Publikováno v:
BMC Pediatrics, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Gynecomastia develops due to the reversed estradiol-to-Testosterone ratio in adolescence, and symptoms typically improve within 2 years. The causes vary widely, including estrogen excess and tumors, and surgical treatment is usual
Externí odkaz:
https://doaj.org/article/ea8c7bd9596844aea6093429c374c026
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-4 (2018)
Abstract Background Kabuki syndrome is characterized by distinctive facial features and varying degrees of growth retardation. It leads to malformations in skeletal, urogenital and cardiac structures; moreover, endocrine conditions such as premature
Externí odkaz:
https://doaj.org/article/c9f4efd602bd46ddb3166ae3075de877
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 2, Pp 107-111 (2018)
Autosomal-dominant hypocalcemia with hypercalciuria (ADHH) is a genetic disease characterized by hypoparathyroidism with hypercalciuria. Most patients with ADHH have calcium-sensing receptor (CaSR) gene mutations. The CaSR gene controls parathyroid s
Externí odkaz:
https://doaj.org/article/2128e61c48fc45c7811ebec2a510591b
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 23, Iss 4, Pp 1-3 (2018)
Various endocrine dysfunctions occur during chemotherapy, including hypoglycemia. However, reports of hypoglycemia associated with 6-mercaptopurine (6-MP) are rare. Herein, we report an 8-year-old boy with severe symptomatic hypoglycemia likely due t
Externí odkaz:
https://doaj.org/article/5e97824a60324a62a22db5f87fcab947