Seneca S - Search Results

1

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. J Inherit Metab Dis. 1996;19(2):115-8. doi: 10.1007/BF01799407. J Inherit Metab Dis. 1996. PMID: 8739943 No abstract available.

2

Importance of sequence analysis in NARP syndrome.

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

3

DNA diagnosis of X-linked adrenoleukodystrophy.

Seneca S, Lissens W. Seneca S, et al. J Inherit Metab Dis. 1995;18 Suppl 1:34-44. doi: 10.1007/BF00711427. J Inherit Metab Dis. 1995. PMID: 9053554 Review.

4

Molecular analysis in 23 Hunter disease families.

Lissens W, Seneca S, Liebaers I. Lissens W, et al. Among authors: seneca s. J Inherit Metab Dis. 1997 Jul;20(3):453-6. doi: 10.1023/a:1005335624386. J Inherit Metab Dis. 1997. PMID: 9266380 Clinical Trial. No abstract available.

5

Pyruvate dehydrogenase E1 alpha deficiency in a family: different clinical presentation in two siblings.

De Meirleir L, Specola N, Seneca S, Lissens W. De Meirleir L, et al. Among authors: seneca s. J Inherit Metab Dis. 1998 Jun;21(3):224-6. doi: 10.1023/a:1005347501111. J Inherit Metab Dis. 1998. PMID: 9686362 No abstract available.

6

A novel mitochondrial transfer RNA proline mutation.

Seneca S, Ceuterik-De Groote C, Van Coster R, De Meirleir L. Seneca S, et al. 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.

7

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: seneca s. Eur J Paediatr Neurol. 2004;8(6):299-306. doi: 10.1016/j.ejpn.2004.07.006. Eur J Paediatr Neurol. 2004. PMID: 15542384

8

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: seneca s. Arch Neurol. 2006 Aug;63(8):1194-8. doi: 10.1001/archneur.63.8.1194. Arch Neurol. 2006. PMID: 16908752

9

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: seneca s. Arch Neurol. 2007 Sep;64(9):1339-43. doi: 10.1001/archneur.64.9.1339. Arch Neurol. 2007. PMID: 17846276

10

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: seneca s. 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

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