Eyskens F - Search Results

1

Roels F, Saudubray JM, Giros M, Mandel H, Eyskens F, Saracibar N, Atares Pueyo B, Prats JM, De Prest B, De Preter K, Pineda M, Krystkowiak P, Gootjes J, Wanders RJ, Espeel M, Poll-The BT. Roels F, et al. Among authors: eyskens f. Adv Exp Med Biol. 2003;544:97-106. doi: 10.1007/978-1-4419-9072-3_14. Adv Exp Med Biol. 2003. PMID: 14713220 No abstract available.

2

Novel mutations in the PEX2 gene of four unrelated patients with a peroxisome biogenesis disorder.

Gootjes J, Elpeleg O, Eyskens F, Mandel H, Mitanchez D, Shimozawa N, Suzuki Y, Waterham HR, Wanders RJ. Gootjes J, et al. Among authors: eyskens f. Pediatr Res. 2004 Mar;55(3):431-6. doi: 10.1203/01.PDR.0000106862.83469.8D. Epub 2003 Nov 19. Pediatr Res. 2004. PMID: 14630978

3

Mitochondrial mosaics in the liver of 3 infants with mtDNA defects.

Roels F, Verloo P, Eyskens F, François B, Seneca S, De Paepe B, Martin JJ, Meersschaut V, Praet M, Scalais E, Espeel M, Smet J, Van Goethem G, Van Coster R. Roels F, et al. Among authors: eyskens f. BMC Clin Pathol. 2009 Jun 5;9:4. doi: 10.1186/1472-6890-9-4. BMC Clin Pathol. 2009. PMID: 19500334 Free PMC article.

4

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: eyskens fj. Kidney Int. 1996 Nov;50(5):1747-52. doi: 10.1038/ki.1996.494. Kidney Int. 1996. PMID: 8914045 Free article.

5

Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines.

Ebberink MS, Mooyer PA, Koster J, Dekker CJ, Eyskens FJ, Dionisi-Vici C, Clayton PT, Barth PG, Wanders RJ, Waterham HR. Ebberink MS, et al. Hum Mutat. 2009 Jan;30(1):93-8. doi: 10.1002/humu.20833. Hum Mutat. 2009. PMID: 18712838

6

Disturbances of valine metabolism in patients with peroxisomal biogenesis disorders.

Eyskens FJ, Lefevere M. Eyskens FJ, et al. Adv Exp Med Biol. 2003;544:73-4. doi: 10.1007/978-1-4419-9072-3_11. Adv Exp Med Biol. 2003. PMID: 14713217 No abstract available.

7

Urinary excretion of purine and pyrimidine metabolites in the neonate.

Van Acker KJ, Eyskens FJ, Verkerk RM, Scharpé SS. Van Acker KJ, et al. Among authors: eyskens fj. Pediatr Res. 1993 Dec;34(6):762-6. doi: 10.1203/00006450-199312000-00012. Pediatr Res. 1993. PMID: 8108189

8

Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy.

Ajit Bolar N, Vanlander AV, Wilbrecht C, Van der Aa N, Smet J, De Paepe B, Vandeweyer G, Kooy F, Eyskens F, De Latter E, Delanghe G, Govaert P, Leroy JG, Loeys B, Lill R, Van Laer L, Van Coster R. Ajit Bolar N, et al. Among authors: eyskens f. Hum Mol Genet. 2013 Jul 1;22(13):2590-602. doi: 10.1093/hmg/ddt107. Epub 2013 Mar 5. Hum Mol Genet. 2013. PMID: 23462291

9

Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12.

De Meirleir L, Seneca S, Lissens W, De Clercq I, Eyskens F, Gerlo E, Smet J, Van Coster R. De Meirleir L, et al. Among authors: eyskens f. J Med Genet. 2004 Feb;41(2):120-4. doi: 10.1136/jmg.2003.012047. J Med Genet. 2004. PMID: 14757859 Free PMC article.

10

Carbohydrate-deficient glycoprotein syndrome with previously unreported features.

Eyskens F, Ceuterick C, Martin JJ, Janssens G, Jaeken J. Eyskens F, et al. Acta Paediatr. 1994 Aug;83(8):892-6. doi: 10.1111/j.1651-2227.1994.tb13166.x. Acta Paediatr. 1994. PMID: 7981572

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