De Meirleir L - Search Results

1

A novel mitochondrial transfer RNA proline mutation.

Seneca S, Ceuterik-De Groote C, Van Coster R, De Meirleir L. Seneca S, et al. Among authors: de meirleir l. J Inherit Metab Dis. 2000 Dec;23(8):853-4. doi: 10.1023/a:1026729223050. J Inherit Metab Dis. 2000. PMID: 11196116 No abstract available.

2

A novel mitochondrial transfer RNA(Asn) mutation causing multiorgan failure.

Meulemans A, Seneca S, Lagae L, Lissens W, De Paepe B, Smet J, Van Coster R, De Meirleir L. Meulemans A, et al. Among authors: de meirleir l, de paepe b. Arch Neurol. 2006 Aug;63(8):1194-8. doi: 10.1001/archneur.63.8.1194. Arch Neurol. 2006. PMID: 16908752

3

Importance of sequence analysis in NARP syndrome.

Seneca S, De Meirleir L, Liebaers I, Lissens W. Seneca S, et al. Among authors: de meirleir l. J Inherit Metab Dis. 1995;18(1):97-8. doi: 10.1007/BF00711391. J Inherit Metab Dis. 1995. PMID: 7623460 No abstract available.

4

A mitochondrial DNA microdeletion in a newborn girl with transient lactic acidosis.

Seneca S, Abramowicz M, Lissens W, Muller MF, Vamos E, de Meirleir L. Seneca S, et al. Among authors: de meirleir l. J Inherit Metab Dis. 1996;19(2):115-8. doi: 10.1007/BF01799407. J Inherit Metab Dis. 1996. PMID: 8739943 No abstract available.

5

A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome.

Seneca S, Verhelst H, De Meirleir L, Meire F, Ceuterick-De Groote C, Lissens W, Van Coster R. Seneca S, et al. Among authors: de meirleir l. Arch Neurol. 2001 Jul;58(7):1113-8. doi: 10.1001/archneur.58.7.1113. Arch Neurol. 2001. PMID: 11448301 Review.

6

Analysis of the mitochondrial encoded subunits of complex I in 20 patients with a complex I deficiency.

Meulemans A, Lissens W, Van Coster R, De Meirleir L, Smet J, Nassogne MC, Liebaers I, Seneca S. Meulemans A, et al. Among authors: de meirleir l. Eur J Paediatr Neurol. 2004;8(6):299-306. doi: 10.1016/j.ejpn.2004.07.006. Eur J Paediatr Neurol. 2004. PMID: 15542384

7

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: de meirleir l, de paepe b. 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

8

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: de meirleir l, de paepe b, de bleecker j. Arch Neurol. 2007 Sep;64(9):1339-43. doi: 10.1001/archneur.64.9.1339. Arch Neurol. 2007. PMID: 17846276

9

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. Among authors: de meirleir l, de paepe b. 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

10

Bilateral striatal necrosis with a novel point mutation in the mitochondrial ATPase 6 gene.

De Meirleir L, Seneca S, Lissens W, Schoentjes E, Desprechins B. De Meirleir L, et al. Pediatr Neurol. 1995 Oct;13(3):242-6. doi: 10.1016/0887-8994(95)00184-h. Pediatr Neurol. 1995. PMID: 8554662

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