Kemp S - Search Results

1

Bezafibrate for X-linked adrenoleukodystrophy.

Engelen M, Tran L, Ofman R, Brennecke J, Moser AB, Dijkstra IM, Wanders RJ, Poll-The BT, Kemp S. Engelen M, et al. Among authors: kemp s. PLoS One. 2012;7(7):e41013. doi: 10.1371/journal.pone.0041013. Epub 2012 Jul 20. PLoS One. 2012. PMID: 22911730 Free PMC article. Clinical Trial.

2

Identification of a two base pair deletion in five unrelated families with adrenoleukodystrophy: a possible hot spot for mutations.

Kemp S, Ligtenberg MJ, van Geel BM, Barth PG, Wolterman RA, Schoute F, Sarde CO, Mandel JL, van Oost BA, Bolhuis PA. Kemp S, et al. Biochem Biophys Res Commun. 1994 Jul 29;202(2):647-53. doi: 10.1006/bbrc.1994.1979. Biochem Biophys Res Commun. 1994. PMID: 8048932

3

Two intronic mutations in the adrenoleukodystrophy gene.

Kemp S, Ligtenberg MJ, van Geel BM, Barth PG, Sarde CO, van Oost BA, Bolhuis PA. Kemp S, et al. Hum Mutat. 1995;6(3):272-3. doi: 10.1002/humu.1380060316. Hum Mutat. 1995. PMID: 8535452 No abstract available.

4

ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophy.

Kemp S, Mooyer PA, Bolhuis PA, van Geel BM, Mandel JL, Barth PG, Aubourg P, Wanders RJ. Kemp S, et al. J Inherit Metab Dis. 1996;19(5):667-74. doi: 10.1007/BF01799844. J Inherit Metab Dis. 1996. PMID: 8892025

5

Gene redundancy and pharmacological gene therapy: implications for X-linked adrenoleukodystrophy.

Kemp S, Wei HM, Lu JF, Braiterman LT, McGuinness MC, Moser AB, Watkins PA, Smith KD. Kemp S, et al. Nat Med. 1998 Nov;4(11):1261-8. doi: 10.1038/3242. Nat Med. 1998. PMID: 9809549

6

Pharmacological induction of peroxisomes in peroxisome biogenesis disorders.

Wei H, Kemp S, McGuinness MC, Moser AB, Smith KD. Wei H, et al. Among authors: kemp s. Ann Neurol. 2000 Mar;47(3):286-96. Ann Neurol. 2000. PMID: 10716247

7

ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.

Kemp S, Pujol A, Waterham HR, van Geel BM, Boehm CD, Raymond GV, Cutting GR, Wanders RJ, Moser HW. Kemp S, et al. Hum Mutat. 2001 Dec;18(6):499-515. doi: 10.1002/humu.1227. Hum Mutat. 2001. PMID: 11748843 Review.

8

A very long-chain acyl-CoA synthetase-deficient mouse and its relevance to X-linked adrenoleukodystrophy.

Heinzer AK, Watkins PA, Lu JF, Kemp S, Moser AB, Li YY, Mihalik S, Powers JM, Smith KD. Heinzer AK, et al. Among authors: kemp s. Hum Mol Genet. 2003 May 15;12(10):1145-54. doi: 10.1093/hmg/ddg126. Hum Mol Genet. 2003. PMID: 12719378

9

Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry.

Valianpour F, Selhorst JJ, van Lint LE, van Gennip AH, Wanders RJ, Kemp S. Valianpour F, et al. Among authors: kemp s. Mol Genet Metab. 2003 Jul;79(3):189-96. doi: 10.1016/s1096-7192(03)00098-2. Mol Genet Metab. 2003. PMID: 12855224

10

Method for measurement of peroxisomal very-long-chain fatty acid beta-oxidation in human skin fibroblasts using stable-isotope-labeled tetracosanoic acid.

Kemp S, Valianpour F, Mooyer PA, Kulik W, Wanders RJ. Kemp S, et al. Clin Chem. 2004 Oct;50(10):1824-6. doi: 10.1373/clinchem.2004.038539. Clin Chem. 2004. PMID: 15388659 No abstract available.

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