Smet J - Search Results

1

A systems biology strategy reveals biological pathways and plasma biomarker candidates for potentially toxic statin-induced changes in muscle.

Laaksonen R, Katajamaa M, Päivä H, Sysi-Aho M, Saarinen L, Junni P, Lütjohann D, Smet J, Van Coster R, Seppänen-Laakso T, Lehtimäki T, Soini J, Oresic M. Laaksonen R, et al. Among authors: smet j. PLoS One. 2006 Dec 20;1(1):e97. doi: 10.1371/journal.pone.0000097. PLoS One. 2006. PMID: 17183729 Free PMC article. Clinical Trial.

2

High-dose statins and skeletal muscle metabolism in humans: a randomized, controlled trial.

Päivä H, Thelen KM, Van Coster R, Smet J, De Paepe B, Mattila KM, Laakso J, Lehtimäki T, von Bergmann K, Lütjohann D, Laaksonen R. Päivä H, et al. Among authors: smet j. Clin Pharmacol Ther. 2005 Jul;78(1):60-8. doi: 10.1016/j.clpt.2005.03.006. Clin Pharmacol Ther. 2005. PMID: 16003294 Clinical Trial.

3

[Application of new techniques for locating the underlying molecular defects in patients with disorders of oxidative phosphorylation].

Van Coster R, Smet J. Van Coster R, et al. Among authors: smet j. Verh K Acad Geneeskd Belg. 2007;69(4):197-211. Verh K Acad Geneeskd Belg. 2007. PMID: 17821958 Review. Dutch.

4

Tigecycline-induced inhibition of mitochondrial DNA translation may cause lethal mitochondrial dysfunction in humans.

Vandecasteele SJ, Seneca S, Smet J, Reynders M, De Ceulaer J, Vanlander AV, van Coster R. Vandecasteele SJ, et al. Among authors: smet j. Clin Microbiol Infect. 2018 Apr;24(4):431.e1-431.e3. doi: 10.1016/j.cmi.2017.08.018. Epub 2017 Sep 1. Clin Microbiol Infect. 2018. PMID: 28870729 Free article.

5

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. Among authors: smet j. Arch Neurol. 2007 Sep;64(9):1339-43. doi: 10.1001/archneur.64.9.1339. Arch Neurol. 2007. PMID: 17846276

6

The aerobic forearm exercise test, a non-invasive tool to screen for mitochondrial disorders.

Meulemans A, Gerlo E, Seneca S, Lissens W, Smet J, Van Coster R, De Meirleir L. Meulemans A, et al. Among authors: smet j. Acta Neurol Belg. 2007 Sep;107(3):78-83. Acta Neurol Belg. 2007. PMID: 18072335

7

A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathy.

Seneca S, Goemans N, Van Coster R, Givron P, Reybrouck T, Sciot R, Meulemans A, Smet J, Van Hove JL. Seneca S, et al. Among authors: smet j. Am J Med Genet A. 2005 Aug 30;137(2):170-5. doi: 10.1002/ajmg.a.30854. Am J Med Genet A. 2005. PMID: 16059939

8

Forearm deoxyhemoglobin and deoxymyoglobin (deoxy[Hb + Mb]) measured by near-infrared spectroscopy (NIRS) using a handgrip test in mitochondrial myopathy.

Celie BM, Boone J, Smet JE, Vanlander AV, De Bleecker JL, Van Coster RN, Bourgois JG. Celie BM, et al. Among authors: smet je. Appl Spectrosc. 2015 Mar;69(3):342-7. doi: 10.1366/14-07604. Epub 2015 Feb 1. Appl Spectrosc. 2015. PMID: 25665184

9

Mass spectrometric identification of mitochondrial oxidative phosphorylation subunits separated by two-dimensional blue-native polyacrylamide gel electrophoresis.

Devreese B, Vanrobaeys F, Smet J, Van Beeumen J, Van Coster R. Devreese B, et al. Among authors: smet j. Electrophoresis. 2002 Aug;23(15):2525-33. doi: 10.1002/1522-2683(200208)23:15<2525::AID-ELPS2525>3.0.CO;2-I. Electrophoresis. 2002. PMID: 12210211

10

A new family with the mitochondrial tRNAGLU gene mutation m.14709T>C presenting with hydrops fetalis.

Meulemans A, Seneca S, Smet J, De Paepe B, Lissens W, Van Coster R, Debeer A, De Meirleir L, Jaeken J. Meulemans A, et al. Among authors: smet j. Eur J Paediatr Neurol. 2007 Jan;11(1):17-20. doi: 10.1016/j.ejpn.2006.10.004. Epub 2006 Dec 11. Eur J Paediatr Neurol. 2007. PMID: 17161635

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