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Resistance to parathyroid hormone in two patients with familial intrahepatic cholestasis: possible involvement of the ATP8B1 gene in calcium regulation via parathyroid hormone.
Nagasaka H, Yorifuji T, Kosugiyama K, Egawa H, Kawai M, Murayama K, Hasegawa M, Sumazaki R, Tsubaki J, Kikuta H, Matsui A, Tanaka K, Matsuura N, Kobayashi K. Nagasaka H, et al. Among authors: matsui a. J Pediatr Gastroenterol Nutr. 2004 Oct;39(4):404-9. doi: 10.1097/00005176-200410000-00018. J Pediatr Gastroenterol Nutr. 2004. PMID: 15448432 No abstract available.
Evaluation of risk for atherosclerosis in Alagille syndrome and progressive familial intrahepatic cholestasis: two congenital cholestatic diseases with different lipoprotein metabolisms.
Nagasaka H, Yorifuji T, Egawa H, Yanai H, Fujisawa T, Kosugiyama K, Matsui A, Hasegawa M, Okada T, Takayanagi M, Chiba H, Kobayashi K. Nagasaka H, et al. Among authors: matsui a. J Pediatr. 2005 Mar;146(3):329-35. doi: 10.1016/j.jpeds.2004.10.047. J Pediatr. 2005. PMID: 15756213
Gradual improvement of liver function after administration of ursodeoxycholic acid in an infant with a novel ABCB11 gene mutation with phenotypic continuum between BRIC2 and PFIC2.
Takahashi A, Hasegawa M, Sumazaki R, Suzuki M, Toki F, Suehiro T, Onigata K, Tomomasa T, Suzuki T, Matsui A, Morikawa A, Kuwano H. Takahashi A, et al. Among authors: matsui a. Eur J Gastroenterol Hepatol. 2007 Nov;19(11):942-6. doi: 10.1097/MEG.0b013e3282ef4795. Eur J Gastroenterol Hepatol. 2007. PMID: 18049162
Clinical heterogeneity of neonatal intrahepatic cholestasis caused by citrin deficiency: case reports from 16 patients.
Tazawa Y, Kobayashi K, Abukawa D, Nagata I, Maisawa S, Sumazaki R, Iizuka T, Hosoda Y, Okamoto M, Murakami J, Kaji S, Tabata A, Lu YB, Sakamoto O, Matsui A, Kanzaki S, Takada G, Saheki T, Iinuma K, Ohura T. Tazawa Y, et al. Among authors: matsui a. Mol Genet Metab. 2004 Nov;83(3):213-9. doi: 10.1016/j.ymgme.2004.06.018. Mol Genet Metab. 2004. PMID: 15542392
813 results