Laatste update: 02/12/2016

Wetenschappelijke publicaties


Publicaties 2009

Quintana E, Gort L, Busquets C, Navarro-Sastre A, Lissens W, Moliner S, Lluch M, Vilaseca MA, De Meirleir L, Ribes A, Briones P; PDH Working Group. Mutational study in the PDHA1 gene of 40 patients suspected of pyruvate dehydrogenase complex deficiency. Clin Genet. 2010 May;77(5):474-82. doi: 10.1111/j.1399-0004.2009.01313.x. Epub 2009 Dec 10. Erratum in: Clin Genet. 2010 Jul;78(1):101. PubMed PMID: 20002461.

Meulemans A, Seneca S, Pribyl T, Smet J, Alderweirldt V, Waeytens A, Lissens W, Van Coster R, De Meirleir L, di Rago JP, Gatti DL, Ackerman SH. Defining the pathogenesis of the human Atp12p W94R mutation using a Saccharomyces cerevisiae yeast model. J Biol Chem. 2010 Feb 5;285(6):4099-109. doi: 10.1074/jbc.M109.046920. Epub 2009 Nov 20. PubMed PMID: 19933271; PubMed Central PMCID: PMC2823550.

Van Biervliet S, Verloo P, Vande Veldel S, Van Winckel M, Smet J, Seneca S, De Meirleir L, Van Coster R. Abdominal pain and vomiting as first sign of mitochondrial disease. Acta Gastroenterol Belg. 2009 Jul-Sep;72(3):365-8. PubMed PMID: 19902874.

Desmyttere S, Bonduelle M, Nekkebroeck J, Roelants M, Liebaers I, De Schepper J. Growth and health outcome of 102 2-year-old children conceived after pre-implantation genetic diagnosis or screening. Early Hum Dev. 2009 Dec;85(12):755-9. doi: 10.1016/j.earlhumdev.2009.10.003. Epub 2009 Nov 5. PubMed PMID: 19896307.

Van Haute L, De Block G, Liebaers I, Sermon K, De Rycke M. Generation of lung epithelial-like tissue from human embryonic stem cells. Respir Res. 2009 Nov 5;10:105. doi: 10.1186/1465-9921-10-105. PubMed PMID: 19891764; PubMed Central PMCID: PMC2777141.

Smet J, Seneca S, De Paepe B, Meulemans A, Verhelst H, Leroy J, De Meirleir L, Lissens W, Van Coster R. Subcomplexes of mitochondrial complex V reveal mutations in mitochondrial DNA. Electrophoresis. 2009 Oct;30(20):3565-72. doi: 10.1002/elps.200900213. PubMed PMID: 19862739.

De Vos A, Staessen C, De Rycke M, Verpoest W, Haentjens P, Devroey P, Liebaers I, Van de Velde H. Impact of cleavage-stage embryo biopsy in view of PGD on human blastocyst implantation: a prospective cohort of single embryo transfers. Hum Reprod. 2009 Dec;24(12):2988-96. doi: 10.1093/humrep/dep251. Epub 2009 Sep 21. PubMed PMID: 19773223.

Liebaers I, Desmyttere S, Verpoest W, De Rycke M, Staessen C, Sermon K, Devroey P, Haentjens P, Bonduelle M. Report on a consecutive series of 581 children born after blastomere biopsy for pre-implantation genetic diagnosis. Hum Reprod. 2010 Jan;25(1):275-82. doi: 10.1093/humrep/dep298. Epub 2009 Aug 27. PubMed PMID: 19713301.

Richardson P, Whittaker S, Rajesh U, Bonduelle M, Morgan J, Garry M, Weston C, Ferguson C, Fligelstone L. Caesarean delivery in a parturient with a femoro-femoral crossover graft and congenital aortic stenosis repaired by the Ross procedure. Int J Obstet Anesth. 2009 Oct;18(4):387-91. doi: 10.1016/j.ijoa.2009.02.018. Epub 2009 Aug 22. PubMed PMID: 19703763.

Verpoest W, Van Landuyt L, Desmyttere S, Cremers A, Devroey P, Liebaers I. The incidence of monozygotic twinning following PGD is not increased. Hum Reprod. 2009 Nov;24(11):2945-50. doi: 10.1093/humrep/dep280. Epub 2009 Aug 6. PubMed PMID: 19661123.

Verpoest W, Haentjens P, De Rycke M, Staessen C, Sermon K, Bonduelle M, Devroey P, Liebaers I. Cumulative reproductive outcome after pre-implantation genetic diagnosis: a report on 1498 couples. Hum Reprod. 2009 Nov;24(11):2951-9. doi: 10.1093/humrep/dep272. Epub 2009 Aug 3. PubMed PMID: 19654112.

Vanneste E, Voet T, Melotte C, Debrock S, Sermon K, Staessen C, Liebaers I, Fryns JP, D'Hooghe T, Vermeesch JR. What next for pre-implantation genetic screening? High mitotic chromosome instability rate provides the biological basis for the low success rate. Hum Reprod. 2009 Nov;24(11):2679-82. doi: 10.1093/humrep/dep266. Epub 2009 Jul 24. PubMed PMID: 19633308; PubMed Central PMCID: PMC2763130.

Geens M, Mateizel I, Sermon K, De Rycke M, Spits C, Cauffman G, Devroey P, Tournaye H, Liebaers I, Van de Velde H. Human embryonic stem cell lines derived from single blastomeres of two 4-cell stage embryos. Hum Reprod. 2009 Nov;24(11):2709-17. doi: 10.1093/humrep/dep262. Epub 2009 Jul 24. PubMed PMID: 19633307; PubMed Central PMCID: PMC2763129.

Konno T, Abe Y, Kawaguchi M, Storm K, Biervliet M, Courtens W, Kono M, Tomita Y, Suzuki T. Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2. Am J Med Genet A. 2009 Aug;149A(8):1773-6. doi: 10.1002/ajmg.a.32964. PubMed PMID: 19610114.

Mateizel I, Spits C, Verloes A, Mertzanidou A, Liebaers I, Sermon K. Characterization of CD30 expression in human embryonic stem cell lines cultured in serum-free media and passaged mechanically. Hum Reprod. 2009 Oct;24(10):2477-89. doi: 10.1093/humrep/dep234. Epub 2009 Jul 7. PubMed PMID: 19584135.

Zecic A, Smet JE, De Praeter CM, Vanhaesebrouck P, Viscomi C, Van Den Broecke C, De Paepe B, Lohse P, Martin JJ, Jackson JG, Campbell CR, De Meirleir LJ, Zeviani M, Seneca SH, Lissens W, Van Coster RN. Lactic acidosis in a newborn with adrenal calcifications. Pediatr Res. 2009 Sep;66(3):317-22. doi: 10.1203/PDR.0b013e3181b40a80. PubMed PMID: 19581830.

Goossens E, De Rycke M, Haentjens P, Tournaye H. DNA methylation patterns of spermatozoa and two generations of offspring obtained after murine spermatogonial stem cell transplantation. Hum Reprod. 2009 Sep;24(9):2255-63. doi: 10.1093/humrep/dep213. Epub 2009 Jun 12. PubMed PMID: 19525299.

Stouffs K, Tournaye H, Liebaers I, Lissens W. Male infertility and the involvement of the X chromosome. Hum Reprod Update. 2009 Nov-Dec;15(6):623-37. doi: 10.1093/humupd/dmp023. Epub 2009 Jun 10. Review. PubMed PMID: 19515807.

Ramos-Arroyo MA, Hualde J, Ayechu A, De Meirleir L, Seneca S, Nadal N, Briones P. Clinical and biochemical spectrum of mitochondrial complex III deficiency caused by mutations in the BCS1L gene. Clin Genet. 2009 Jun;75(6):585-7. doi: 10.1111/j.1399-0004.2009.01160.x. PubMed PMID: 19508421.

De Schepper J, Belva F, Schiettecatte J, Anckaert E, Tournaye H, Bonduelle M. Testicular growth and tubular function in prepubertal boys conceived by intracytoplasmic sperm injection. Horm Res. 2009;71(6):359-63. doi: 10.1159/000223421. Epub 2009 Jun 9. PubMed PMID: 19506394.

Roels F, Verloo P, Eyskens F, François B, Seneca S, De Paepe B, Martin JJ, Meersschaut V, Praet M, Scalais E, Espeel M, Smet J, Van Goethem G, Van Coster R. Mitochondrial mosaics in the liver of 3 infants with mtDNA defects. BMC Clin Pathol. 2009 Jun 5;9:4. doi: 10.1186/1472-6890-9-4. PubMed PMID: 19500334; PubMed Central PMCID: PMC2706255.

Keymolen K, Staessen C, Verpoest W, Michiels A, Bonduelle M, Haentjens P, Vanderelst J, Liebaers I. A proposal for reproductive counselling in carriers of Robertsonian translocations: 10 years of experience with pre-implantation genetic diagnosis. Hum Reprod. 2009 Sep;24(9):2365-71. doi: 10.1093/humrep/dep201. Epub 2009 Jun 3. PubMed PMID: 19493873.

Brachet C, Boros E, Tenoutasse S, Lissens W, Andry G, Martin P, Bergmann P, Heinrichs C. Association of parathyroid adenoma and familial hypocalciuric hypercalcaemia in a teenager. Eur J Endocrinol. 2009 Jul;161(1):207-10. doi: 10.1530/EJE-09-0257. Epub 2009 May 7. PubMed PMID: 19423559.

Gil-Borlado MC, González-Hoyuela M, Blázquez A, García-Silva MT, Gabaldón T, Manzanares J, Vara J, Martín MA, Seneca S, Arenas J, Ugalde C. Pathogenic mutations in the 5' untranslated region of BCS1L mRNA in mitochondrial complex III deficiency. Mitochondrion. 2009 Sep;9(5):299-305. doi: 10.1016/j.mito.2009.04.001. Epub 2009 Apr 21. PubMed PMID: 19389488.

Devroey P, Fauser BC, Diedrich K; Evian Annual Reproduction (EVAR) Workshop Group 2008. Approaches to improve the diagnosis and management of infertility. Hum Reprod Update. 2009 Jul-Aug;15(4):391-408. doi: 10.1093/humupd/dmp012. Epub 2009 Apr 20. Review. PubMed PMID: 19380415; PubMed Central PMCID: PMC2691653.

De Rademaeker M, Verpoest W, De Rycke M, Seneca S, Sermon K, Desmyttere S, Bonduelle M, Van der Elst J, Devroey P, Liebaers I. Pre-implantation genetic diagnosis for myotonic dystrophy type 1: upon request to child. Eur J Hum Genet. 2009 Nov;17(11):1403-10. doi: 10.1038/ejhg.2009.56. Epub 2009 Apr 15. PubMed PMID: 19367318; PubMed Central PMCID: PMC2986672.

Kirchhoff M, Bisgaard AM, Stoeva R, Dimitrov B, Gillessen-Kaesbach G, Fryns JP, Rose H, Grozdanova L, Ivanov I, Keymolen K, Fagerberg C, Tranebjaerg L, Skovby F, Stefanova M. Phenotype and 244k array-CGH characterization of chromosome 13q deletions: an update of the phenotypic map of 13q21.1-qter. Am J Med Genet A. 2009 May;149A(5):894-905. doi: 10.1002/ajmg.a.32814. PubMed PMID: 19363806.

De Paepe B, Smet J, Lammens M, Seneca S, Martin JJ, De Bleecker J, De Meirleir L, Lissens W, Van Coster R. Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects. J Clin Pathol. 2009 Feb;62(2):172-6. doi: 10.1136/jcp.2008.061267. PubMed PMID: 19181635.