User menu

Search

Displaying 1 - 25 of 169 results.

Pages

    • Journal article
    Cricopharyngeal achalasia: case reports and review of the literature.
    De Caluwe, D Reding, Raymond[UCL] Nassogne, Marie-Cécile[UCL] de Ville de Goyet, J Clapuyt, Philippe[UCL] Otte, Jean-Bernard[UCL] (1999) European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift für Kinderchirurgie — Vol. 9, no. 2, p. 109-12 (1999)
    • Journal article
    Whipple disease confined to the central nervous system in childhood.
    Duprez, Thierry[UCL] Grandin, Cécile[UCL] Bonnier, Christine Thauvoy, Christian[UCL] Gadisseux, J F Dutrieux, J L Evrard, Philippe[UCL] (1996) AJNR. American journal of neuroradiology — Vol. 17, no. 8, p. 1589-91 (1996)
    • Journal article
    Polymicrogyria and motor neuropathy in micro syndrome
    Nassogne, Marie-Cécile[UCL] Henrot, B. Saint-Martin, C Kadhim, Hazim[UCL] Dobyns, WB Sebire, G (2000) Neuropediatrics : journal of pediatric neurobiology, neurology and neurosurgery — Vol. 31, no. 4, p. 218-221 (2000)
    • Journal article
    Les myopathies congénitales
    Christiaens, F[UCL] Van den Bergh, Peter[UCL] (2014) Louvain médical — (2014)
    • Journal article
    Towards a suggestive facial dysmorphism in adenylosuccinate lyase deficiency?
    Holder-Espinasse, M Marie, S. Bourrouillou, G Ceballos-Picot, I Nassogne, Marie-Cécile[UCL] Faivre, L. Amiel, J Munnich, A. Vincent, Marie-Françoise[UCL] Cormier-Daire, V (2002) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 39, no. 6, p. 440-442 (2002)
    • Journal article
    Neural correlates of symbolic number comparison in developmental dyscalculia
    Mussolin, Christophe[UCL] De Volder, Anne[UCL] Grandin, Cécile[UCL] Schlogel, Xavier[UCL] Nassogne, Marie-Cécile[UCL] Noël, Marie-Pascale[UCL] (2010) Journal of Cognitive Neuroscience — Vol. 22, no. 5, p. 860-874 (2010)
    • Journal article
    Le syndrome de Prader-Willi
    Beauloye, Véronique[UCL] Jodogne, Nathalie[UCL] Dassy, Martine[UCL] Bonnier, Christine[UCL] Castelein, Sara[UCL] François, Geneviève[UCL] Godding, Véronique[UCL] Renders, Anne[UCL] Symann, Sophie[UCL] Yüksel, Demet[UCL] Revencu, Nicole[UCL] Tauber, Maïthé (2013) Louvain médical — Vol. 132, no.N° spécial, p. 463 - 467 (2013)
    • Journal article
    Tyrosinemia Type III detected via neonatal screening: Management and outcome.
    Heylen, Evelyne[UCL] Scherer, Gerd Vincent, Marie-Françoise[UCL] Marie, Sandrine[UCL] Fischer, Judith Nassogne, Marie-Cécile[UCL] (2012) Molecular Genetics and Metabolism — Vol. 107, no. 3, p. 605-607 (2012)

Pages