Kobayashi K - Search Results

1

Adult onset type II citrullinemia as a cause of non-alcoholic steatohepatitis.

Takagi H, Hagiwara S, Hashizume H, Kanda D, Sato K, Sohara N, Kakizaki S, Takahashi H, Mori M, Kaneko H, Ohwada S, Ushikai M, Kobayashi K, Saheki T. Takagi H, et al. Among authors: kobayashi k. J Hepatol. 2006 Jan;44(1):236-9. doi: 10.1016/j.jhep.2005.08.024. Epub 2005 Sep 26. J Hepatol. 2006. PMID: 16278034

2

Mitochondrial aspartate glutamate carrier (citrin) deficiency as the cause of adult-onset type II citrullinemia (CTLN2) and idiopathic neonatal hepatitis (NICCD).

Saheki T, Kobayashi K. Saheki T, et al. Among authors: kobayashi k. J Hum Genet. 2002;47(7):333-41. doi: 10.1007/s100380200046. J Hum Genet. 2002. PMID: 12111366 Review.

3

Citrin deficiency as a cause of chronic liver disorder mimicking non-alcoholic fatty liver disease.

Komatsu M, Yazaki M, Tanaka N, Sano K, Hashimoto E, Takei Y, Song YZ, Tanaka E, Kiyosawa K, Saheki T, Aoyama T, Kobayashi K. Komatsu M, et al. Among authors: kobayashi k. J Hepatol. 2008 Nov;49(5):810-20. doi: 10.1016/j.jhep.2008.05.016. Epub 2008 Jun 10. J Hepatol. 2008. PMID: 18620775

4

Adult-onset type II citrullinemia and idiopathic neonatal hepatitis caused by citrin deficiency: involvement of the aspartate glutamate carrier for urea synthesis and maintenance of the urea cycle.

Saheki T, Kobayashi K, Iijima M, Horiuchi M, Begum L, Jalil MA, Li MX, Lu YB, Ushikai M, Tabata A, Moriyama M, Hsiao KJ, Yang Y. Saheki T, et al. Among authors: kobayashi k. Mol Genet Metab. 2004 Apr;81 Suppl 1:S20-6. doi: 10.1016/j.ymgme.2004.01.006. Mol Genet Metab. 2004. PMID: 15050970 Review.

5

[Molecular basis of citrin deficiency].

Kobayashi K, Saheki T. Kobayashi K, et al. Seikagaku. 2004 Dec;76(12):1543-59. Seikagaku. 2004. PMID: 15675368 Review. Japanese. No abstract available.

6

Variant clinical courses of 2 patients with neonatal intrahepatic cholestasis who have a novel mutation of SLC25A13.

Takaya J, Kobayashi K, Ohashi A, Ushikai M, Tabata A, Fujimoto S, Yamato F, Saheki T, Kobayashi Y. Takaya J, et al. Among authors: kobayashi y, kobayashi k. Metabolism. 2005 Dec;54(12):1615-9. doi: 10.1016/j.metabol.2005.06.009. Metabolism. 2005. PMID: 16311094

7

A case of adult-onset type II citrullinemia--deterioration of clinical course after infusion of hyperosmotic and high sugar solutions.

Takahashi H, Kagawa T, Kobayashi K, Hirabayashi H, Yui M, Begum L, Mine T, Takagi S, Saheki T, Shinohara Y. Takahashi H, et al. Among authors: kobayashi k. Med Sci Monit. 2006 Feb;12(2):CS13-5. Epub 2006 Jan 26. Med Sci Monit. 2006. PMID: 16449956

8

Adult-onset type II citrullinemia associated with idopathic hypertriglyceridemia as a preceding feature.

Terada R, Yamamoto K, Kobayashi K, Sakaguchi K, Iwasaki Y, Saheki T, Shiratori Y. Terada R, et al. Among authors: kobayashi k. J Gastroenterol Hepatol. 2006 Oct;21(10):1634-5. doi: 10.1111/j.1440-1746.2006.04339.x. J Gastroenterol Hepatol. 2006. PMID: 16928234 No abstract available.

9

Identification of 13 novel mutations including a retrotransposal insertion in SLC25A13 gene and frequency of 30 mutations found in patients with citrin deficiency.

Tabata A, Sheng JS, Ushikai M, Song YZ, Gao HZ, Lu YB, Okumura F, Iijima M, Mutoh K, Kishida S, Saheki T, Kobayashi K. Tabata A, et al. Among authors: kobayashi k. J Hum Genet. 2008;53(6):534-545. doi: 10.1007/s10038-008-0282-2. Epub 2008 Apr 5. J Hum Genet. 2008. PMID: 18392553

10

A patient with adult-onset type II citrullinemia on long-term hemodialysis: reversal of clinical symptoms and brain MRI findings.

Oshiro S, Kochinda T, Tana T, Yamazato M, Kobayashi K, Komine Y, Muratani H, Saheki T, Iseki K, Takishita S. Oshiro S, et al. Among authors: kobayashi k. Am J Kidney Dis. 2002 Jan;39(1):189-92. doi: 10.1053/ajkd.2002.29915. Am J Kidney Dis. 2002. PMID: 11774119

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