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Displaying 1 - 25 of 105 results.

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    • 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
    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
    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
    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)
    • Speech
    A case of D-2 hydroxyglutaric aciduria
    Paquay, Stéphanie[UCL] Nassogne, Marie-Cécile[UCL] (2013) SSIEM Academy — Lyon, France
    • Journal article
    A new case of syndromic craniosynostosis with cryptic 19p13.2-p13.13 deletion.
    Lysy, Philippe[UCL] Ravoet, Marie Wustefeld, Sandrine[UCL] Bernard, Pierre[UCL] Nassogne, Marie-Cécile[UCL] Wyns, Elisabeth Sibille, Catherine[UCL] (2009) American Journal of Medical Genetics. Part A — Vol. 149A, no.11, p. 2564-2568 (2009)
    • Journal article
    Comparison of antigen contents in co-cultures by an in situ immunoradiometric assay.
    Nassogne, Marie-Cécile[UCL] Baudhuin, Pierre[UCL] Courtoy, Pierre J.[UCL] (1999) Biology of the cell / under the auspices of the European Cell Biology Organization — Vol. 91, no. 8, p. 629-36 (1999)
    • Journal article
    Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome.
    Nassogne, Marie-Cécile[UCL] Sharrard, Mark Hertz-Pannier, Lucie Armengaud, Didier Touati, Guy Delonlay-Debeney, Pascale Zerah, Michel Brunelle, Francis Saudubray, Jean-Marie (2002) Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery — Vol. 18, no. 12, p. 729-31 (2002)

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