Suchergebnisse - Cheol Woo Ko

Delayed diagnosis of pituitary stalk interruption syndrome with severe recurrent hyponatremia caused by adrenal insufficiency von Kyung Mi Jang, Cheol Woo Ko

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A de novo KMT2D mutation in a girl with Kabuki syndrome associated with endocrine symptoms: a case report von Jung-Eun Moon, Su-Jeong Lee, Cheol Woo Ko

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Various endocrine disorders in children with t(13;14)(q10;q10) Robertsonian translocation von Byung Ho Choi, Uk Hyun Kim, Kun Soo Lee, Cheol Woo Ko

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Severe recurrent nocturnal hypoglycemia during chemotherapy with 6-mercaptopurine in a child with acute lymphoblastic leukemia von Eun Mi Cho, Jung Eun Moon, Soo Jung Lee, Cheol Woo Ko

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Combined surgical and medical treatment in an adolescent with severe gynecomastia due to excessive estradiol secretion: a case report von Jung-Eun Moon, Cheol Woo Ko, Jung Dug Yang, Joon Seok Lee

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Changes of antithroglobulin antibody in children with congenital hypothyroidism von Eun Mi Cho, Uk Hyun Kim, Byung Ho Choi, Cheol Woo Ko

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Clinical manifestations of IgA nephropathy combined with thin glomerular basement membrane nephropathy in children von Young Ju Hwang, Dong Sub Kim, Cheol Woo Ko, Min Hyun Cho, Tae In Park

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An Alport syndrome boy with Van Wyk-Grumbach syndrome induced by prolonged untreated congenital hypothyroidism von Su-Jeong Lee, Jung-Eun Moon, Gi-Min Lee, Min-Hyun Cho, Cheol Woo Ko

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A cell function study on calcium regulation of a novel calcium-sensing receptor mutation (p.Tyr825Phe) von Jung Eun Moon, Hee-Young Yang, Gabbine Wee, Suk-Hyun ParK, Cheol Woo Ko

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Initial steroid regimen in idiopathic nephrotic syndrome can be shortened based on duration to first remission von Hee Sun Baek, Ki-Soo Park, Hee Gyung Kang, Cheol Woo Ko, Min Hyun Cho

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a novel variant of gene in a neonate with congenital hypoparathyroidism von Jung-Eun Moon, Su-Jeong Lee, Suk-Hyun Park, Jinsup Kim, Dong-Kyu Jin, Cheol Woo Ko

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Polyclonal gammopathy related to renal bleeding in a peritoneal dialysis patient von Eun-Mi Cho, Hye-Hyun Moon, Young-Ju Hwang, Seung-Jin Lee, Cheol Woo Ko, Min Hyun Cho

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Clinical, endocrinological, and molecular features of four Korean cases of cytochrome P450 oxidoreductase deficiency von 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

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