- Hereditary Spherocytosis Coexisting with UDP-Glucuronosyltransferase Deficiency Highly Suggestive of Crigler-Najjar Syndrome Type II
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Iijima S, Ohzeki T, Maruo Y
- KMID: 1779679
- Yonsei Med J.
- 2011 Mar;52(2):369-372.
- doi: 10.3349/ymj.2011.52.2.369
Patients with co-existing hereditary spherocytosis (HS) and UDP-glucuronosyltransferase 1A1 (UGT1A1) deficiency as Gilbert's syndrome (GS) have been reported, and previous studies have demonstrated an increased risk for developing gallstones in... -
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- KISS1 Gene Polymorphisms in Korean Girls with Central Precocious Puberty
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Rhie YJ, Lee KH, Ko JM, Lee WJ, Kim JH, Kim HS
- KMID: 2129608
- J Korean Med Sci.
- 2014 Aug;29(8):1120-1125.
- doi: 10.3346/jkms.2014.29.8.1120
Kisspeptin/G-protein couple receptor-54 (GPR54) system plays a key role in the activation of the gonadotropic axis at puberty. Central precocious puberty (CPP) is caused by the premature activation of hypothalamic... -
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