Lissens W - Search Results

1

Early onset Huntington disease: a neuronal degeneration syndrome.

Seneca S, Fagnart D, Keymolen K, Lissens W, Hasaerts D, Debulpaep S, Desprechins B, Liebaers I, De Meirleir L. Seneca S, et al. Among authors: lissens w. Eur J Pediatr. 2004 Dec;163(12):717-21. doi: 10.1007/s00431-004-1537-3. Eur J Pediatr. 2004. PMID: 15338298

2

Preimplantation genetic diagnosis for Huntington's disease with exclusion testing.

Sermon K, De Rijcke M, Lissens W, De Vos A, Platteau P, Bonduelle M, Devroey P, Van Steirteghem A, Liebaers I. Sermon K, et al. Among authors: lissens w. Eur J Hum Genet. 2002 Oct;10(10):591-8. doi: 10.1038/sj.ejhg.5200865. Eur J Hum Genet. 2002. PMID: 12357329

3

SYCP3 mutations are uncommon in patients with azoospermia.

Stouffs K, Lissens W, Tournaye H, Van Steirteghem A, Liebaers I. Stouffs K, et al. Among authors: lissens w. Fertil Steril. 2005 Oct;84(4):1019-20. doi: 10.1016/j.fertnstert.2005.04.033. Fertil Steril. 2005. PMID: 16213863

4

Preimplantation diagnosis for Huntington's disease (HD): clinical application and analysis of the HD expansion in affected embryos.

Sermon K, Goossens V, Seneca S, Lissens W, De Vos A, Vandervorst M, Van Steirteghem A, Liebaers I. Sermon K, et al. Among authors: lissens w. Prenat Diagn. 1998 Dec;18(13):1427-36. doi: 10.1002/(sici)1097-0223(199812)18:13<1427::aid-pd493>3.0.co;2-3. Prenat Diagn. 1998. PMID: 9949443

5

Cerebral palsy and pyruvate dehydrogenase deficiency: identification of two new mutations in the E1alpha gene.

Lissens W, Vreken P, Barth PG, Wijburg FA, Ruitenbeek W, Wanders RJ, Seneca S, Liebaers I, De Meirleir L. Lissens W, et al. Eur J Pediatr. 1999 Oct;158(10):853-7. doi: 10.1007/s004310051222. Eur J Pediatr. 1999. PMID: 10486093

6

PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome.

Sermon K, Seneca S, De Rycke M, Goossens V, Van de Velde H, De Vos A, Platteau P, Lissens W, Van Steirteghem A, Liebaers I. Sermon K, et al. Among authors: lissens w. Mol Cell Endocrinol. 2001 Oct 22;183 Suppl 1:S77-85. doi: 10.1016/s0303-7207(01)00572-x. Mol Cell Endocrinol. 2001. PMID: 11576738

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: lissens w. 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 single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) region.

Lissens W, Arena A, Seneca S, Rafi M, Sorge G, Liebaers I, Wenger D, Fiumara A. Lissens W, et al. Hum Mutat. 2007 Jul;28(7):742. doi: 10.1002/humu.9500. Hum Mutat. 2007. PMID: 17579360

9

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. Among authors: lissens w. Pediatr Neurol. 1995 Oct;13(3):242-6. doi: 10.1016/0887-8994(95)00184-h. Pediatr Neurol. 1995. PMID: 8554662

10

Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG.

Sermon K, Seneca S, Vanderfaeillie A, Lissens W, Joris H, Vandervorst M, Van Steirteghem A, Liebaers I. Sermon K, et al. Among authors: lissens w. Prenat Diagn. 1999 Dec;19(13):1223-30. Prenat Diagn. 1999. PMID: 10660959

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