Choeh K - Search Results

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US identification of the anal sphincter complex and levator ani muscle in neonates: infracoccygeal approach.

Han TI, Kim IO, Kim WS, Chung JY, Choeh K, Song MK, Yoon YG. Han TI, et al. Among authors: choeh k. Radiology. 2000 Nov;217(2):392-4. doi: 10.1148/radiology.217.2.r00nv21392. Radiology. 2000. PMID: 11058633

Rhabdoid tumour of the kidney: imaging findings.

Han TI, Kim MJ, Yoon HK, Chung JY, Choeh K. Han TI, et al. Among authors: choeh k. Pediatr Radiol. 2001 Apr;31(4):233-7. doi: 10.1007/s002470000417. Pediatr Radiol. 2001. PMID: 11321739

Screening of nine SLC25A13 mutations: their frequency in patients with citrin deficiency and high carrier rates in Asian populations.

Kobayashi K, Bang Lu Y, Xian Li M, Nishi I, Hsiao KJ, Choeh K, Yang Y, Hwu WL, Reichardt JK, Palmieri F, Okano Y, Saheki T. Kobayashi K, et al. Among authors: choeh k. Mol Genet Metab. 2003 Nov;80(3):356-9. doi: 10.1016/S1096-7192(03)00140-9. Mol Genet Metab. 2003. PMID: 14680984

A genetic factor for age-related cataract: identification and characterization of a novel galactokinase variant, "Osaka," in Asians.

Okano Y, Asada M, Fujimoto A, Ohtake A, Murayama K, Hsiao KJ, Choeh K, Yang Y, Cao Q, Reichardt JK, Niihira S, Imamura T, Yamano T. Okano Y, et al. Among authors: choeh k. Am J Hum Genet. 2001 Apr;68(4):1036-42. doi: 10.1086/319512. Epub 2001 Feb 23. Am J Hum Genet. 2001. PMID: 11231902 Free PMC article.

Novel mutations, including the second most common in Japan, in the beta-hexosaminidase alpha subunit gene, and a simple screening of Japanese patients with Tay-Sachs disease.

Tanaka A, Fujimaru M, Choeh K, Isshiki G. Tanaka A, et al. Among authors: choeh k. J Hum Genet. 1999;44(2):91-5. doi: 10.1007/s100380050116. J Hum Genet. 1999. PMID: 10083731

Two mutations remote from an exon/intron junction in the beta-hexosaminidase beta-subunit gene affect 3'-splice site selection and cause Sandhoff disease.

Fujimaru M, Tanaka A, Choeh K, Wakamatsu N, Sakuraba H, Isshiki G. Fujimaru M, et al. Among authors: choeh k. Hum Genet. 1998 Oct;103(4):462-9. doi: 10.1007/s004390050851. Hum Genet. 1998. PMID: 9856491

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