中文 | English
Return
Total: 4 , 1/1
Show Home Prev Next End page: GO
MeSH:(Adrenal Hyperplasia, Congenital/*diagnosis/drug therapy)

1.Relationships of Basal Level of Serum 17-Hydroxyprogesterone with that of Serum Androstenedione and Their Stimulated Responses to a Low Dose of ACTH in Young Adult Patients with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency.

Min Jae KANG ; Shin Mi KIM ; Young Ah LEE ; Choong Ho SHIN ; Sei Won YANG

Journal of Korean Medical Science 2011;26(11):1454-1460

2.A novel missense mutation, GGC(Arg454) --> TGC(Cys), of CYP11B1 gene identified in a Chinese family with steroid 11beta-hydroxylase deficiency.

Zheng-qin YE ; Man-na ZHANG ; Hui-jie ZHANG ; Jing-jing JIANG ; Xiao-ying LI ; Ke-qin ZHANG

Chinese Medical Journal 2010;123(10):1264-1268

3.Clinical Features of Congenital Adrenal Insufficiency Including Growth Patterns and Significance of ACTH Stimulation Test.

Ji Won KOH ; Gu Hwan KIM ; Han Wook YOO ; Jeesuk YU

Journal of Korean Medical Science 2013;28(11):1650-1656

4.A Case of Congenital Adrenal Hyperplasia Mimicking Cushing's Syndrome.

Hye Jeong KIM ; Mira KANG ; Jae Hyeon KIM ; Sun Wook KIM ; Jae Hoon CHUNG ; Yong Ki MIN ; Moon Kyu LEE ; Kwang Won KIM ; Myung Shik LEE

Journal of Korean Medical Science 2012;27(11):1439-1443

Sort by Result Analysis

Display Mode

Output Records




File Type





Total: 4 , 1/1 Show Home Prev Next End page: GO