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Displaying 4 results.
    • Journal article
    Tumor Spectrum in Children With Noonan Syndrome and SOS1 or RAF1 Mutations
    Denayer, Ellen[UCL] Devriendt, Koen[UCL] de Ravel, Thomy[UCL] Van Buggenhout, Griet[UCL] Smeets, Eric[UCL] Francois, Inge[UCL] Sznajer, Yves Craen, Margarita Leventopoulos, George Mutesa, Leon Vandecasseye, Willy[UCL] Massa, Guy Kayserili, Hulya Sciot, Raf[UCL] Fryns, Jean-Pierre[UCL] Legius, Eric[UCL] (2010) Genes, Chromosomes & Cancer — Vol. 49, no. 3, p. 242-252 (2010)
    • Journal article
    Expanding the CHARGE Geno-Phenotype: A Girl with Novel CHD7 Deletion, Hypogonadotropic Hypogonadism, and Agenesis of Uterus and Ovaries.
    Reynaert, Nele de Zegher, Francis Francois, Inge Devriendt, Koenraad Beckers, Dominique[UCL] Casteels, Kristina (2016) Hormone Research in Paediatrics : from developmental endocrinology to clinical research — Vol. 85, no. 4, p. 288-290 (2016)
    • Journal article
    Evaluation of the hypothalamic-pituitary-adrenal axis and its relationship with central respiratory dysfunction in children with Prader-Willi syndrome.
    Beauloye, Véronique[UCL] Dhondt, Karlien Buysse, Wesley Nyakasane, Adolphe[UCL] Zech, Francis[UCL] De Schepper, Jean Van Aken, Sara De Waele, Kathleen Craen, Margarita Gies, Inge Francois, Inge Beckers, Dominique[UCL] Desloovere, An François, Geneviève[UCL] Cools, Martine (2015) Orphanet Journal of Rare Diseases — Vol. 10, no. 1, p. 106 [1-8] (2015)
    • Journal article
    Clinical presentation and outcome of children with central diabetes insipidus associated with a self-limited or transient pituitary stalk thickening, diagnosed as infundibuloneurohypophysitis.
    Schaefers, Jacqueline Cools, Martine De Waele, Kathleen Gies, Inge Beauloye, Véronique[UCL] Lysy, Philippe[UCL] Francois, Inge Beckers, Dominique[UCL] De Schepper, Jean (2017) Clinical Endocrinology — Vol. 87, no. 2, p. 171-176 (2017)