Similar articles for PMID: 15448432

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1969	1
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2017	4
2018	5
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1

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. 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.

2

A case of progressive familial intrahepatic cholestasis type 1 with compound heterozygous mutations of ATP8B1.

Numakura C, Abukawa D, Kimura T, Tanabe S, Hayasaka K. Numakura C, et al. Pediatr Int. 2011 Feb;53(1):107-10. doi: 10.1111/j.1442-200X.2010.03238.x. Pediatr Int. 2011. PMID: 21342337 No abstract available.

3

[The bones and parathyroid hormone].

Gennari C. Gennari C. Minerva Med. 1979 Jun 8;70(27):1945-9. Minerva Med. 1979. PMID: 221861 Italian. No abstract available.

4

Effects of short-term maximal work on plasma calcium, parathyroid hormone, osteocalcin and biochemical markers of collagen metabolism.

Kristoffersson A, Hultdin J, Holmlund I, Thorsen K, Lorentzon R. Kristoffersson A, et al. Int J Sports Med. 1995 Apr;16(3):145-9. doi: 10.1055/s-2007-972982. Int J Sports Med. 1995. PMID: 7649703

5

Type I procollagen propeptide in patients on CAPD: its relationships with bone histology, osteocalcin, and parathyroid hormone.

Joffe P, Heaf JG, Jensen LT. Joffe P, et al. Nephrol Dial Transplant. 1995 Oct;10(10):1912-7. Nephrol Dial Transplant. 1995. PMID: 8592603

6

Effects of long-term treatment with growth hormone on bone and mineral metabolism in children with growth hormone deficiency.

Saggese G, Baroncelli GI, Bertelloni S, Cinquanta L, Di Nero G. Saggese G, et al. J Pediatr. 1993 Jan;122(1):37-45. doi: 10.1016/s0022-3476(05)83484-5. J Pediatr. 1993. PMID: 8419613

7

NR1H4 analysis in patients with progressive familial intrahepatic cholestasis, drug-induced cholestasis or intrahepatic cholestasis of pregnancy unrelated to ATP8B1, ABCB11 and ABCB4 mutations.

Davit-Spraul A, Gonzales E, Jacquemin E. Davit-Spraul A, et al. Clin Res Hepatol Gastroenterol. 2012 Dec;36(6):569-73. doi: 10.1016/j.clinre.2012.08.008. Epub 2012 Nov 9. Clin Res Hepatol Gastroenterol. 2012. PMID: 23142591

8

ATP8B1 mutations in British cases with intrahepatic cholestasis of pregnancy.

Müllenbach R, Bennett A, Tetlow N, Patel N, Hamilton G, Cheng F, Chambers J, Howard R, Taylor-Robinson SD, Williamson C. Müllenbach R, et al. Gut. 2005 Jun;54(6):829-34. doi: 10.1136/gut.2004.058115. Gut. 2005. PMID: 15888793 Free PMC article.

9

Progressive familial intrahepatic cholestasis: genetic disorders of biliary transporters.

Harris MJ, Le Couteur DG, Arias IM. Harris MJ, et al. J Gastroenterol Hepatol. 2005 Jun;20(6):807-17. doi: 10.1111/j.1440-1746.2005.03743.x. J Gastroenterol Hepatol. 2005. PMID: 15946126 Review.

10

A Novel Truncation Mutation in ATP8B1 Gene in Progressive Familial Intrahepatic Cholestasis.

Sharma A, Poddar U, Agnihotry S, Aggarwal R. Sharma A, et al. Indian Pediatr. 2016 Dec 15;53(12):1099-1101. Indian Pediatr. 2016. PMID: 28064265 Free article.

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