Houwen RH - Search Results

1

[From gene to disease; Wilson disease: copper storage due to mutations in ATP7B].

Stapelbroek JM, Ploos van Amstel JK, van Hattum J, van den Berg LH, Klomp LW, Houwen RH. Stapelbroek JM, et al. Among authors: houwen rh. Ned Tijdschr Geneeskd. 2003 Mar 29;147(13):603-5. Ned Tijdschr Geneeskd. 2003. PMID: 12701394 Review. Dutch.

2

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis.

Stapelbroek JM, Bollen CW, van Amstel JK, van Erpecum KJ, van Hattum J, van den Berg LH, Klomp LW, Houwen RH. Stapelbroek JM, et al. Among authors: houwen rh. J Hepatol. 2004 Nov;41(5):758-63. doi: 10.1016/j.jhep.2004.07.017. J Hepatol. 2004. PMID: 15519648

3

Long-term exclusive zinc monotherapy in symptomatic Wilson disease: experience in 17 patients.

Linn FH, Houwen RH, van Hattum J, van der Kleij S, van Erpecum KJ. Linn FH, et al. Among authors: houwen rh. Hepatology. 2009 Nov;50(5):1442-52. doi: 10.1002/hep.23182. Hepatology. 2009. PMID: 19731238

4

Reduced expression of ATP7B affected by Wilson disease-causing mutations is rescued by pharmacological folding chaperones 4-phenylbutyrate and curcumin.

van den Berghe PV, Stapelbroek JM, Krieger E, de Bie P, van de Graaf SF, de Groot RE, van Beurden E, Spijker E, Houwen RH, Berger R, Klomp LW. van den Berghe PV, et al. Among authors: houwen rh. Hepatology. 2009 Dec;50(6):1783-95. doi: 10.1002/hep.23209. Hepatology. 2009. PMID: 19937698

5

FIC1 disease: a spectrum of intrahepatic cholestatic disorders.

van Mil SW, Klomp LW, Bull LN, Houwen RH. van Mil SW, et al. Among authors: houwen rh. Semin Liver Dis. 2001 Nov;21(4):535-44. doi: 10.1055/s-2001-19034. Semin Liver Dis. 2001. PMID: 11745041 Review.

6

H714Q mutation in Wilson disease is associated with late, neurological presentation.

Houwen RH, Juyn J, Hoogenraad TU, Ploos van Amstel JK, Berger R. Houwen RH, et al. J Med Genet. 1995 Jun;32(6):480-2. doi: 10.1136/jmg.32.6.480. J Med Genet. 1995. PMID: 7666402 Free PMC article.

7

Wilson disease.

Houwen RH, van Hattum J, Hoogenraad TU. Houwen RH, et al. Neth J Med. 1993 Aug;43(1-2):26-37. Neth J Med. 1993. PMID: 8232692 Review. No abstract available.

8

Genetics of familial intrahepatic cholestasis syndromes.

van Mil SW, Houwen RH, Klomp LW. van Mil SW, et al. Among authors: houwen rh. J Med Genet. 2005 Jun;42(6):449-63. doi: 10.1136/jmg.2004.026187. J Med Genet. 2005. PMID: 15937079 Free PMC article. Review.

9

The copper connection.

Linn FH, van Erpecum KJ, Klomp LW, Houwen RH. Linn FH, et al. Among authors: houwen rh. Eur J Neurol. 2009 Oct;16(10):1073-4. doi: 10.1111/j.1468-1331.2009.02732.x. Epub 2009 Jun 29. Eur J Neurol. 2009. PMID: 19566898 No abstract available.

10

Fic1 is expressed at apical membranes of different epithelial cells in the digestive tract and is induced in the small intestine during postnatal development of mice.

van Mil SW, van Oort MM, van den Berg IE, Berger R, Houwen RH, Klomp LW. van Mil SW, et al. Among authors: houwen rh. Pediatr Res. 2004 Dec;56(6):981-7. doi: 10.1203/01.PDR.0000145564.06791.D1. Epub 2004 Oct 20. Pediatr Res. 2004. PMID: 15496606

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