Laatste update: 02/12/2016

Wetenschappelijke publicaties


Publicaties 2001


Van Coster R, Smet J, George E, De Meirleir L, Seneca S, Van Hove J, Sebire G, Verhelst H, De Bleecker J, Van Vlem B, Verloo P, Leroy J. Blue native polyacrylamide gel electrophoresis: a powerful tool in diagnosis of oxidative phosphorylation defects. Pediatr Res. 2001 Nov;50(5):658-65. PubMed PMID: 11641463.

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. PGD in the lab for triplet repeat diseases - myotonic dystrophy, Huntington's disease and Fragile-X syndrome. Mol Cell Endocrinol. 2001 Oct 22;183 Suppl 1:S77-85. PubMed PMID: 11576738.

Georgiou I, Sermon K, Lissens W, De Vos A, Platteau P, Lolis D, Van Steirteghem A, Liebaers I. Pre-implantation genetic diagnosis for spinal and bulbar muscular atrophy (SBMA). Hum Genet. 2001 Jun;108(6):494-8. PubMed PMID: 11499674.

Manning M, Lissens W, Weidner W, Liebaers I. DNA methylation analysis in immature testicular sperm cells at different developmental stages. Urol Int. 2001;67(2):151-5. PubMed PMID: 11490210.

Seneca S, Verhelst H, De Meirleir L, Meire F, Ceuterick-De Groote C, Lissens W, Van Coster R. A new mitochondrial point mutation in the transfer RNA(Leu) gene in a patient with a clinical phenotype resembling Kearns-Sayre syndrome. Arch Neurol. 2001 Jul;58(7):1113-8. Review. PubMed PMID: 11448301.

Olivennes F, Mannaerts B, Struijs M, Bonduelle M, Devroey P. Perinatal outcome of pregnancy after GnRH antagonist (ganirelix) treatment during ovarian stimulation for conventional IVF or ICSI: a preliminary report. Hum Reprod. 2001 Aug;16(8):1588-91. PubMed PMID: 11473947.

De Baere E, Dixon MJ, Small KW, Jabs EW, Leroy BP, Devriendt K, Gillerot Y, Mortier G, Meire F, Van Maldergem L, Courtens W, Hjalgrim H, Huang S, Liebaers I, Van Regemorter N, Touraine P, Praphanphoj V, Verloes A, Udar N, Yellore V, Chalukya M, Yelchits S, De Paepe A, Kuttenn F, Fellous M, Veitia R, Messiaen L. Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation. Hum Mol Genet. 2001 Jul 15;10(15):1591-600. PubMed PMID: 11468277.

Taillandier A, Lia-Baldini AS, Mouchard M, Robin B, Muller F, Simon-Bouy B, Serre JL, Bera-Louville A, Bonduelle M, Eckhardt J, Gaillard D, Myhre AG, Körtge-Jung S, Larget-Piet L, Malou E, Sillence D, Temple IK, Viot G, Mornet E. Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia. Hum Mutat. 2001;18(1):83-4. PubMed PMID: 11438998.

Van Landuyt L, Lissens W, Stouffs K, Tournaye H, Van Steirteghem A, Liebaers I, Blagosklonova O, Bresson JL. The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis. Mol Hum Reprod. 2001 Jul;7(7):691-3. PubMed PMID: 11420393.

Stouffs K, Lissens W, Van Landuyt L, Tournaye H, Van Steirteghem A, Liebaers I. Characterization of the genomic organization, localization and expression of four PRY genes (PRY1, PRY2, PRY3 and PRY4). Mol Hum Reprod. 2001 Jul;7(7):603-10. PubMed PMID: 11420382.

Manning M, Lissens W, Liebaers I, Van Steirteghem A, Weidner W. Imprinting analysis in spermatozoa prepared for intracytoplasmic sperm injection (ICSI). Int J Androl. 2001 Apr;24(2):87-94. PubMed PMID: 11298842.

Bonduelle M. [Neurological history - Charles-Edouard Brown-Séquard]. Rev Neurol (Paris). 2001 Feb;157(2):234-8. French. PubMed PMID: 11283471.


De Rycke M, Van de Velde H, Sermon K, Lissens W, De Vos A, Vandervorst M, Vanderfaeillie A, Van Steirteghem A, Liebaers I. Pre-implantation genetic diagnosis for sickle-cell anemia and for beta-thalassemia. Prenat Diagn. 2001 Mar;21(3):214-22. PubMed PMID: 11260611.