Laatste update: 02/12/2016

Wetenschappelijke publicaties

Publicaties 2000

Seneca S, Ceuterik-De Groote C, Van Coster R, De Meirleir L. A novel mitochondrial transfer RNA proline mutation. J Inherit Metab Dis. 2000 Dec;23(8):853-4. PubMed PMID: 11196116.

Van de Velde H, De Vos A, Sermon K, Staessen C, De Rycke M, Van Assche E, Lissens W, Vandervorst M, Van Ranst H, Liebaers I, Van Steirteghem A. Embryo implantation after biopsy of one or two cells from cleavage-stage embryos with a view to pre-implantation genetic diagnosis. Prenat Diagn. 2000 Dec;20(13):1030-7. PubMed PMID: 11180226.

Cardozo AK, De Meirleir L, Liebaers I, Lissens W. Analysis of exonic mutations leading to exon skipping in patients with pyruvate dehydrogenase E1 alpha deficiency. Pediatr Res. 2000 Dec;48(6):748-53. PubMed PMID: 11102541.

Sermon K, Henderix P, Lissens W, De Vos A, Vandervorst M, Vanderfaeillie A, Vamos E, Van Steirteghem A, Liebaers I. Pre-implantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiency. Mol Hum Reprod. 2000 Dec;6(12):1165-8. PubMed PMID: 11101700.

Geraedts J, Handyside A, Harper J, Liebaers I, Sermon K, Staessen C, Thornhill A, Viville S, Wilton L; European Society of Human Reproduction and Embryology Pre-implantation Genetic Diagnosis Consortium Steering Committee. ESHRE pre-implantation genetic diagnosis (PGD) consortium: data collection II (May 2000). Hum Reprod. 2000 Dec;15(12):2673-83. PubMed PMID: 11098044.

Janssens K, Gershoni-Baruch R, Guañabens N, Migone N, Ralston S, Bonduelle M, Lissens W, Van Maldergem L, Vanhoenacker F, Verbruggen L, Van Hul W. Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease. Nat Genet. 2000 Nov;26(3):273-5. PubMed PMID: 11062463.

Manning M, Lissens W, Bonduelle M, Camus M, De Rijcke M, Liebaers I, Van Steirteghem A. Study of DNA-methylation patterns at chromosome 15q11-q13 in children born after ICSI reveals no imprinting defects. Mol Hum Reprod. 2000 Nov;6(11):1049-53. PubMed PMID: 11044469.

De Catte L, Liebaers I, Foulon W. Outcome of twin gestations after first trimester chorionic villus sampling. Obstet Gynecol. 2000 Nov;96(5 Pt 1):714-20. PubMed PMID: 11042306.

Vandervors M, Staessen C, Sermon K, De Vos A, Van de Velde H, Van Assche E, Bonduelle M, Vanderfaellie A, Lissens W, Tournaye H, Devroey P, Van Steirteghem A, Liebaers I. The Brussels' experience of more than 5 years of clinical pre-implantation genetic diagnosis. Hum Reprod Update. 2000 Jul-Aug;6(4):364-73. PubMed PMID: 10972523.

De Vos A, Sermon K, Van de Velde H, Joris H, Vandervorst M, Lissens W, De Paepe A, Liebaers I, Van Steirteghem A. Two pregnancies after pre-implantation genetic diagnosis for osteogenesis imperfecta type I and type IV. Hum Genet. 2000 Jun;106(6):605-13. PubMed PMID: 10942108.

Nogueira D, Staessen C, Van de Velde H, Van Steirteghem A. Nuclear status and cytogenetics of embryos derived from in vitro-matured oocytes. Fertil Steril. 2000 Aug;74(2):295-8. PubMed PMID: 10927047.

Goossens V, Sermon K, Lissens W, Vandervorst M, Vanderfaeillie A, De Rijcke M, De Vos A, Henderix P, Van De Velde H, Van Steirteghem A, Liebaers I. Clinical application of pre-implantation genetic diagnosis for cystic fibrosis. Prenat Diagn. 2000 Jul;20(7):571-81. PubMed PMID: 10913957.

Keymolen K, Van Damme-Lombaerts R, Verloes A, Fryns JP. Distal limb deficiencies, oral involvement, and renal defect: report of a third patient and confirmation of a distinct entity. Am J Med Genet. 2000 Jul 3;93(1):19-21. PubMed PMID: 10861677.

Devriendt K, Keymolen K, Roelen L, Van Goethem G, Meireleire J, Fryns JP. Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism. Clin Dysmorphol. 2000 Apr;9(2):111-4. PubMed PMID: 10826622.

Janssens K, Gershoni-Baruch R, Van Hul E, Brik R, Guañabens N, Migone N, Verbruggen LA, Ralston SH, Bonduelle M, Van Maldergem L, Vanhoenacker F, Van Hul W. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13. J Med Genet. 2000 Apr;37(4):245-9. PubMed PMID: 10745041; PubMed Central PMCID: PMC1734563.

Van Landuyt L, Lissens W, Stouffs K, Tournaye H, Liebaers I, Van Steirteghem A. Validation of a simple Yq deletion screening programme in an ICSI candidate population. Mol Hum Reprod. 2000 Apr;6(4):291-7. PubMed PMID: 10729309.

Lissens W, De Meirleir L, Seneca S, Liebaers I, Brown GK, Brown RM, Ito M, Naito E, Kuroda Y, Kerr DS, Wexler ID, Patel MS, Robinson BH, Seyda A. Mutations in the X-linked pyruvate dehydrogenase (E1) alpha subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency. Hum Mutat. 2000;15(3):209-19. Review. PubMed PMID: 10679936.