Zobrazeno 1 - 10
of 264
pro vyhledávání: '"Sung Yoon, Cho"'
Autor:
Ga young Bae, Insung Kim, Juyoung Sung, JiHoon Hwang, Min-Sun Kim, Ji-Hye Park, Sung Yoon Cho
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 5, Pp 344-346 (2024)
Externí odkaz:
https://doaj.org/article/36aec7d15d114d62ac8123b71cbbf3db
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 1, Pp 67-69 (2024)
Externí odkaz:
https://doaj.org/article/a6d61c8879a04961a4ac0b7d91960b0b
Autor:
Eujin Choi, Min-Sun Kim, Juhee Cho, Sooyeon Kim, Eun Kyung Kwon, Youngha Kim, Danbee Kang, Sung Yoon Cho
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Insulin injections are stressful but necessary for people with diabetes. This study aimed to develop and validate the Distress of Self-Injection (DSI) scale for patients with diabetes aged ≥ 10 years. We created a questionnaire to evaluate
Externí odkaz:
https://doaj.org/article/2bb5cdb7d183455f86fe1ba3b58487d1
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 28, Iss Suppl 1, Pp S1-S2 (2023)
Externí odkaz:
https://doaj.org/article/2b86e953ec63477f9775983bb94c8d0d
Autor:
Minji Im, Ari Song, Jiyeon Kim, Min-Sun Kim, Sae-Mi Lee, Mi Jin Kim, Sung Yoon Cho, Dong-Kyu Jin
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 27, Iss 3, Pp 229-235 (2022)
Wilson disease (WD) is a relatively common genetic hepatic disease in children and is characterized by excessive copper accumulation, predominantly in the liver and brain. It is an autosomal recessive disease caused by an ATP7B mutation that causes b
Externí odkaz:
https://doaj.org/article/a7cb551c04b24bd08b38f19c71ec32b5
Autor:
Young Ah Lee, Ahreum Kwon, Jae Hyun Kim, Hyo-Kyoung Nam, Jae-Ho Yoo, Jung Sub Lim, Sung Yoon Cho, Won Kyoung Cho, Kye Shik Shim
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 27, Iss 1, Pp 5-14 (2022)
The Committee on Pediatric Bone Health of the Korean Society of Pediatric Endocrinology has newly developed evidence-based clinical practice guidelines for optimizing bone health in Korean children and adolescents. These guidelines present recommenda
Externí odkaz:
https://doaj.org/article/17dc4e7103804b528c0ee64417e8aa35
Autor:
Hyojung Park, Min-Sun Kim, Jiyeon Kim, Sae-Mi Lee, Sung Yoon Cho, Eun-Gyong Yoo, Dong-Kyu Jin
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 27, Iss 1, Pp 73-77 (2022)
Diabetic ketoacidosis (DKA) is a medically fatal condition in poorly controlled hyperglycemia or newly diagnosed diabetes mellitus. Severe hypertriglyceridemia (HTG) is an uncommon complication of DKA and can be associated with acute pancreatitis (AP
Externí odkaz:
https://doaj.org/article/832da1d3853f435bb919451faa88e5ec
Publikováno v:
Medicine; 10/18/2024, Vol. 103 Issue 42, p1-7, 7p
Autor:
Piero Pavone, Xena Giada Pappalardo, Naira Mustafa, Sung Yoon Cho, Dong Kyu Jin, Gemma Incorpora, Raffaele Falsaperla, Simona Domenica Marino, Giovanni Corsello, Enrico Parano, Martino Ruggieri
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-11 (2022)
Abstract Background Alternating of Childhood (AHC) is an uncommon and complex disorder characterized by age of onset before 18 months with recurrent hemiplegia of one or either sides of the body or quadriplegia. The disorder is mainly caused by mutat
Externí odkaz:
https://doaj.org/article/860c8ce952474fad8d239f8abc246a64
Autor:
Ari Song, Minji Im, Min-Sun Kim, Eu Seon Noh, Chiwoo Kim, Jahyun Jang, Sae-Mi Lee, Chang-Seok Ki, Sung Yoon Cho, Dong-Kyu Jin
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 28, Iss 1, Pp 67-72 (2022)
Coffin-Lowry syndrome (CLS, OMIM # 303600) is a rare X-linked disorder caused by mutations in RPS6KA3. CLS is characterized by facial dysmorphism, digit abnormalities, developmental delays, growth retardation, and progressive skeletal changes in male
Externí odkaz:
https://doaj.org/article/2c7a73e1f338406a9c811f673589a668