Kerckaert I - Search Results

1

Peroxisome mosaicism in the livers of peroxisomal deficiency patients.

Espeel M, Mandel H, Poggi F, Smeitink JA, Wanders RJ, Kerckaert I, Schutgens RB, Saudubray JM, Poll-The BT, Roels F. Espeel M, et al. Among authors: kerckaert i. Hepatology. 1995 Aug;22(2):497-504. Hepatology. 1995. PMID: 7635418

2

Hepatocellular peroxisomes in human alcoholic and drug-induced hepatitis: a quantitative study.

De Craemer D, Kerckaert I, Roels F. De Craemer D, et al. Among authors: kerckaert i. Hepatology. 1991 Nov;14(5):811-7. doi: 10.1002/hep.1840140512. Hepatology. 1991. PMID: 1937386

3

Hepatic peroxisomes in isolated hyperpipecolic acidaemia: evidence supporting its classification as a single peroxisomal enzyme deficiency.

Kerckaert I, Poll-The BT, Espeel M, Duran M, Roeleveld AB, Wanders RJ, Roels F. Kerckaert I, et al. Virchows Arch. 2000 May;436(5):459-65. doi: 10.1007/s004280050473. Virchows Arch. 2000. PMID: 10881739

4

Peroxisome mosaics in the liver of patients and the regulation of peroxisome expression in rat hepatocyte cultures.

Roels F, Tytgat T, Beken S, Giros M, Espeel M, De Prest B, Kerckaert I, Pàmpols T, Rogiers V. Roels F, et al. Among authors: kerckaert i. Ann N Y Acad Sci. 1996 Dec 27;804:502-15. doi: 10.1111/j.1749-6632.1996.tb18640.x. Ann N Y Acad Sci. 1996. PMID: 8993568 No abstract available.

5

Biogenesis of peroxisomes in fetal liver.

Espeel M, Depreter M, Nardacci R, D'Herde K, Kerckaert I, Stefanini S, Roels F. Espeel M, et al. Among authors: kerckaert i. Microsc Res Tech. 1997 Dec 1;39(5):453-66. doi: 10.1002/(SICI)1097-0029(19971201)39:5<453::AID-JEMT8>3.0.CO;2-H. Microsc Res Tech. 1997. PMID: 9408912 Review.

6

Alterations of hepatic peroxisomes in tyrosinaemia type I: return to fetal type?

Kerckaert I, de Koning TJ, Poll-The BT, Roels F. Kerckaert I, et al. J Inherit Metab Dis. 1998 Jun;21(3):186-90. doi: 10.1023/a:1005351129336. J Inherit Metab Dis. 1998. PMID: 9686353 No abstract available.

7

Hyperoxaluria with hyperglycoluria not due to alanine:glyoxylate aminotransferase defect: a novel type of primary hyperoxaluria.

Van Acker KJ, Eyskens FJ, Espeel MF, Wanders RJ, Dekker C, Kerckaert IO, Roels F. Van Acker KJ, et al. Among authors: kerckaert io. Kidney Int. 1996 Nov;50(5):1747-52. doi: 10.1038/ki.1996.494. Kidney Int. 1996. PMID: 8914045 Free article.

8

Isolated dihydroxyacetonephosphate-acyl-transferase deficiency in rhizomelic chondrodysplasia punctata: clinical presentation, metabolic and histological findings.

Hebestreit H, Wanders RJ, Schutgens RB, Espeel M, Kerckaert I, Roels F, Schmausser B, Schrod L, Marx A. Hebestreit H, et al. Among authors: kerckaert i. Eur J Pediatr. 1996 Dec;155(12):1035-9. doi: 10.1007/BF02532526. Eur J Pediatr. 1996. PMID: 8956940

9

Hepatocyte polarity and the peroxisomal compartment: a comparative study.

Depreter M, Walker T, De Smet K, Beken S, Kerckaert I, Rogiers V, Roels F. Depreter M, et al. Among authors: kerckaert i. Histochem J. 2002 Mar-Apr;34(3-4):139-51. doi: 10.1023/a:1020990414190. Histochem J. 2002. PMID: 12495220

10

Peroxisomal beta-oxidation from endogenous substrates. Demonstration through H2O2 production in the unanaesthetized mouse.

Van den Branden C, Kerckaert I, Roels F. Van den Branden C, et al. Among authors: kerckaert i. Biochem J. 1984 Mar 15;218(3):697-702. doi: 10.1042/bj2180697. Biochem J. 1984. PMID: 6372785 Free PMC article.

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