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Displaying 6 results.
    • Journal article
    ESHRE Preimplantation Genetic Diagnosis (PGD) Consortium: preliminary assessment of data from January 1997 to September 1998
    Geraedts, J Handyside, A Harper, J. C.[UCL] Liebaers, I. Sermon, K Staessen, C Thornhill, A. Vanderfaeillie, A. Viville, S. (1999) Human Reproduction — Vol. 14, no. 12, p. 3138-3148 (1999)
    • Journal article
    Pyruvate-dehydrogenase Deficiency - Clinical and Biochemical-diagnosis
    Demeirleir, L. Lissens, W. Denis, R. Wayenberg, JL. Michotte, A. Brucher, Jean-Marie[UCL] Vamos, E. Gerlo, E. Liebaers, I. (1993) Pediatric Neurology — Vol. 9, no. 3, p. 216-220 (1993)
    • Journal article
    Pitfalls in the diagnosis of mtDNA mutations
    Seneca, S Van den Bergh, Peter[UCL] Lissens, W. Liebaers, I. Nassogne, Marie-Cécile[UCL] Benatar, A De Meirleir, L. (1998) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 35, no. 11, p. 963-964 (1998)
    • Journal article
    A D255H substitution in the arylsulphatase A gene of two unrelated Belgian patients with late-infantile metachromatic leukodystrophy
    Lissens, W. Vervoort, R Vanregemorter, N. VanBogaert, P Freund, M. Dumoulin, Christine[UCL] Seneca, S Liebaers, I. (1996) Journal of Inherited Metabolic Disease — Vol. 19, no. 6, p. 782-786 (1996)
    • Journal article
    Neuropathological Findings of a Patient With Pyruvate Dehydrogenase-e1-alpha Deficiency Presenting As a Cerebral Lactic-acidosis
    Michotte, A. Demeirleir, L. Lissens, W. Denis, R. Wayenberg, JL. Liebaers, I. Brucher, Jean-Marie[UCL] (1993) Acta Neuropathologica — Vol. 85, no. 6, p. 674-678 (1993)
    • Journal article
    Prenatal-diagnosis of Hunter Syndrome Using Fetal Plasma
    Lissens, W. Vanlierde, M. Decaluwe, J. Foulon, W. Evrard, Philippe[UCL] Vanhoof, F. Freund, M. Liebaers, I. (1988) Prenatal Diagnosis — Vol. 8, no. 1, p. 59-62 (1988)