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Displaying 13 results.
    • 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)
    • Speech
    Early involvement of corpus callosum in late infantile form of metachromatic leukodystropity
    Nassogne, Marie-Cécile[UCL] Clapuyt, Philippe[UCL] Vermylen, Christiane[UCL] Vincent, Marie-Françoise[UCL] Lissens, W. van der Knaap, M. S. (2007) —
    • Journal article
    Hypoceruloplasminemia and Ultrastructural-changes Resembling Wilsons-disease in Non-alcoholic Liver Steatosis - a Clinical and Pathological-study of 5 Cases
    Geubel, André[UCL] Grégoire, Vincent[UCL] Rahier, Jacques[UCL] Lissens, W. Dive, Charles[UCL] (1988) Liver — Vol. 8, no. 5, p. 299-306 (1988)
    • 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)
    • Speech
    Camurati-Engelmann disease is caused by mutations in the TGFB1 gene
    Janssens, K Gershoni-Baruch, R Guanabens, N Migone, N. Ralston, SH MacPherson, H Bonduelle, M. Lissens, W. Van Maldergem, L. Vanhoenacker, F. Verbruggen, L. Van Hul, W. (2001) —
    • 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)
    • Speech
    Retinitis pigmentosa and adult-onset neurological deterioration revealing Sanfilippo a disease
    Nassogne, Marie-Cécile[UCL] Jeanjean, Anne[UCL] Grandin, Cécile[UCL] Vincent, Marie-Françoise[UCL] Kestens, C. Lissens, W. (2008) —
    • 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)
    • Speech
    Gene Deletions and Point Mutations Leading To Type-1 Antithrombin Deficiency in 6 Belgian Kindreds
    Jochmans, Koen[UCL] Lissens, W. Capel, P. Chatelain, Bernard Meeus, Peter[UCL] Osselaer, Jean-Claude[UCL] Vermylen, I. Dewaele, Magali[UCL] Liebaers, I. (1995) —
    • Journal article
    Hypoceruloplasminemia and ultrastructural changes resembling Wilson's disease in nonalcoholic liver steatosis. A clinical and pathological study of five cases.
    Geubel, André[UCL] Grégoire, Vincent[UCL] Rahier, Jacques[UCL] Lissens, W. Dive, Charles[UCL] (1988) Liver — Vol. 8, no. 5, p. 299-306 (1988)
    • Speech
    Hypoceruloplasminemia and Nonalcoholic Liver Steatosis
    Grégoire, Vincent[UCL] Geubel, André[UCL] Lievens, M. Lissens, W. Dive, Charles[UCL] (1987) —
    • Speech
    Heterozygosity for the Wilsons-disease (wd) Gene and Nonalcoholic Liver Steatosis
    Grégoire, Vincent[UCL] Geubel, André[UCL] Rahier, Jacques[UCL] Lievens, M. Lissens, W. Dive, Charles[UCL] (1987) —
    • 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)