Laatste update: 02/12/2016

Wetenschappelijke publicaties


Publicaties 2003

Vernaeve V, Bonduelle M, Tournaye H, Camus M, Van Steirteghem A, Devroey P. Pregnancy outcome and neonatal data of children born after ICSI using testicular sperm in obstructive and non-obstructive azoospermia. Hum Reprod. 2003 Oct;18(10):2093-7. PubMed PMID: 14507827.

Geuns E, De Rycke M, Van Steirteghem A, Liebaers I. Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and pre-implantation embryos. Hum Mol Genet. 2003 Nov 15;12(22):2873-9. Epub 2003 Sep 18. PubMed PMID: 14500540.

Staessen C, Tournaye H, Van Assche E, Michiels A, Van Landuyt L, Devroey P, Liebaers I, Van Steirteghem A. PGD in 47,XXY Klinefelter's syndrome patients. Hum Reprod Update. 2003 Jul-Aug;9(4):319-30. Review. PubMed PMID: 12926526.

Joris H, De Vos A, Janssens R, Devroey P, Liebaers I, Van Steirteghem A. Comparison of the results of human embryo biopsy and outcome of PGD after zona drilling using acid Tyrode medium or a laser. Hum Reprod. 2003 Sep;18(9):1896-902. PubMed PMID: 12923146.

Temperley RJ, Seneca SH, Tonska K, Bartnik E, Bindoff LA, Lightowlers RN, Chrzanowska-Lightowlers ZM. Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria. Hum Mol Genet. 2003 Sep 15;12(18):2341-8. Epub 2003 Jul 22. PubMed PMID: 12915481.

De Meirleir L, Seneca S, Damis E, Sepulchre B, Hoorens A, Gerlo E, García Silva MT, Hernandez EM, Lissens W, Van Coster R. Clinical and diagnostic characteristics of complex III deficiency due to mutations in the BCS1L gene. Am J Med Genet A. 2003 Aug 30;121A(2):126-31. PubMed PMID: 12910490.

Goossens V, Sermon K, Lissens W, De Rycke M, Saerens B, De Vos A, Henderix P, Van de Velde H, Platteau P, Van Steirteghem A, Devroey P, Liebaers I. Improving clinical pre-implantation genetic diagnosis for cystic fibrosis by duplex PCR using two polymorphic markers or one polymorphic marker in combination with the detection of the DeltaF508 mutation. Mol Hum Reprod. 2003 Sep;9(9):559-67. PubMed PMID: 12900515.

Gao HZ, Kobayashi K, Tabata A, Tsuge H, Iijima M, Yasuda T, Kalkanoglu HS, Dursun A, Tokatli A, Coskun T, Trefz FK, Skladal D, Mandel H, Seidel J, Kodama S, Shirane S, Ichida T, Makino S, Yoshino M, Kang JH, Mizuguchi M, Barshop BA, Fuchinoue S, Seneca S, Zeesman S, Knerr I, Rodés M, Wasant P, Yoshida I, De Meirleir L, Abdul Jalil M, Begum L, Horiuchi M, Katunuma N, Nakagawa S, Saheki T. Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients. Hum Mutat. 2003 Jul;22(1):24-34. PubMed PMID: 12815590.

De Vos A, Sermon K, De Rijcke M, Goossens V, Henderix P, Van Ranst N, Platteau P, Lissens W, Devroey P, Van Steirteghem A, Liebaers I. Pre-implantation genetic diagnosis for Charcot-Marie-Tooth disease type 1A. Mol Hum Reprod. 2003 Jul;9(7):429-35. PubMed PMID: 12802050.

Van Coster R, Seneca S, Smet J, Van Hecke R, Gerlo E, Devreese B, Van Beeumen J, Leroy JG, De Meirleir L, Lissens W. Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II. Am J Med Genet A. 2003 Jul 1;120A(1):13-8. PubMed PMID: 12794685.

Sock E, Pagon RA, Keymolen K, Lissens W, Wegner M, Scherer G. Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia. Hum Mol Genet. 2003 Jun 15;12(12):1439-47. PubMed PMID: 12783851.

Platteau P, Staessen C, Liebaers I, Van Steirteghem A, Devroey P. "Floating denominators"--effect of verification bias on accuracy estimates for pre-implantation diagnosis. Fertil Steril. 2003 Apr;79(4):1041-2; author reply 1042. PubMed PMID: 12749456.

Bonduelle M, Ponjaert I, Steirteghem AV, Derde MP, Devroey P, Liebaers I. Developmental outcome at 2 years of age for children born after ICSI compared with children born after IVF. Hum Reprod. 2003 Feb;18(2):342-50. PubMed PMID: 12571172.

Kolibianakis E, Osmanagaoglu K, De Catte L, Camus M, Bonduelle M, Liebaers I, Van Steirteghem A, Devroey P. Prenatal genetic testing by amniocentesis appears to result in a lower risk of fetal loss than chorionic villus sampling in singleton pregnancies achieved by intracytoplasmic sperm injection. Fertil Steril. 2003 Feb;79(2):374-8. PubMed PMID: 12568848.