Van Coster RN - Search Results

1

Lactic acidosis in a newborn with adrenal calcifications.

Zecic A, Smet JE, De Praeter CM, Vanhaesebrouck P, Viscomi C, Van Den Broecke C, De Paepe B, Lohse P, Martin JJ, Jackson JG, Campbell CR, De Meirleir LJ, Zeviani M, Seneca SH, Lissens W, Van Coster RN. Zecic A, et al. Among authors: van coster rn. Pediatr Res. 2009 Sep;66(3):317-22. doi: 10.1203/PDR.0b013e3181b40a80. Pediatr Res. 2009. PMID: 19581830 Free PMC article.

2

Neonatal lactic acidosis explained by LARS2 defect.

De Paepe B, Smet J, Kopajtich R, Prokisch H, Van Coster R, Vanlander A. De Paepe B, et al. Pediatr Res. 2023 Mar;93(4):740-743. doi: 10.1038/s41390-022-02169-7. Epub 2022 Jun 24. Pediatr Res. 2023. PMID: 35750896 No abstract available.

3

Diagnostic value of immunostaining in cultured skin fibroblasts from patients with oxidative phosphorylation defects.

de Paepe B, Smet J, Leroy JG, Seneca S, George E, Matthys D, van Maldergem L, Scalais E, Lissens W, de Meirleir L, Meulemans A, van Coster R. de Paepe B, et al. Pediatr Res. 2006 Jan;59(1):2-6. doi: 10.1203/01.pdr.0000191294.34122.ab. Epub 2005 Dec 2. Pediatr Res. 2006. PMID: 16327006

4

Complex III staining in blue native polyacrylamide gels.

Smet J, De Paepe B, Seneca S, Lissens W, Kotarsky H, De Meirleir L, Fellman V, Van Coster R. Smet J, et al. J Inherit Metab Dis. 2011 Jun;34(3):741-7. doi: 10.1007/s10545-011-9315-7. Epub 2011 Apr 12. J Inherit Metab Dis. 2011. PMID: 21484424

5

Fluorescence imaging of mitochondria in cultured skin fibroblasts: a useful method for the detection of oxidative phosphorylation defects.

De Paepe B, Smet J, Vanlander A, Seneca S, Lissens W, De Meirleir L, Vandewoestyne M, Deforce D, Rodenburg RJ, Van Coster R. De Paepe B, et al. Pediatr Res. 2012 Sep;72(3):232-40. doi: 10.1038/pr.2012.84. Epub 2012 Jun 22. Pediatr Res. 2012. PMID: 22728747

6

Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II.

Van Coster R, Seneca S, Smet J, Van Hecke R, Gerlo E, Devreese B, Van Beeumen J, Leroy JG, De Meirleir L, Lissens W. Van Coster R, et al. Am J Med Genet A. 2003 Jul 1;120A(1):13-8. doi: 10.1002/ajmg.a.10202. Am J Med Genet A. 2003. PMID: 12794685

7

Two novel mitochondrial DNA mutations in muscle tissue of a patient with limb-girdle myopathy.

Meulemans A, De Paepe B, De Bleecker J, Smet J, Lissens W, Van Coster R, De Meirleir L, Seneca S. Meulemans A, et al. Arch Neurol. 2007 Sep;64(9):1339-43. doi: 10.1001/archneur.64.9.1339. Arch Neurol. 2007. PMID: 17846276

8

Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA.

Smet J, Seneca S, De Paepe B, Meulemans A, Verhelst H, Leroy J, De Meirleir L, Lissens W, Van Coster R. Smet J, et al. Electrophoresis. 2009 Oct;30(20):3565-72. doi: 10.1002/elps.200900213. Electrophoresis. 2009. PMID: 19862739

9

Unraveling the mechanisms behind the enhanced MTT conversion by irradiated breast cancer cells.

Blockhuys S, Vanhoecke B, Smet J, De Paepe B, Van Coster R, Bracke M, De Wagter C. Blockhuys S, et al. Radiat Res. 2013 Apr;179(4):433-43. doi: 10.1667/RR3070.1. Epub 2013 Mar 6. Radiat Res. 2013. PMID: 23465060

10

Effect of resveratrol on cultured skin fibroblasts from patients with oxidative phosphorylation defects.

De Paepe B, Vandemeulebroecke K, Smet J, Vanlander A, Seneca S, Lissens W, Van Hove JL, Deschepper E, Briones P, Van Coster R. De Paepe B, et al. Phytother Res. 2014 Feb;28(2):312-6. doi: 10.1002/ptr.4988. Epub 2013 Apr 26. Phytother Res. 2014. PMID: 23620374

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