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Displaying 1 - 25 of 95 results.

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    • Journal article
    De Novo Atypical Haemolytic Uremic Syndrome after Kidney Transplantation.
    Devresse, Arnaud[UCL] de Meyer, Martine[UCL] Aydin, Selda[UCL] Dahan, Karin[UCL] Kanaan, Nada[UCL] (2018) Case Reports in Nephrology — Vol. 2018, p. 1727986 (2018)
    • Speech
    Detection of large rearrangements by MLPA in severe hemophilia A patients
    Lannoy, Nathalie[UCL] Abinet, Isabelle[UCL] Lambert, Catherine[UCL] Vermylen, Christiane[UCL] Dahan, Karin[UCL] Hermans, Cédric[UCL] (2009) XXII Congress of the International Society of Thrombosis and Haemostasis — (United States) Boston, MA
    • Speech
    Proposition for a multi-step mutation detection in haemophilia A
    Lannoy, Nathalie[UCL] Abinet, Isabelle[UCL] Verellen-Dumoulin, Christine[UCL] Vermylen, Christiane[UCL] Hermans, Cédric[UCL] Dahan, Karin[UCL] (2007) XXI Congress of the International Society on Thrombosis and Haemostasis — (Switzerland) Geneva
    • Journal article
    Blau syndrome associated with a CARD15/NOD2 mutation.
    Snyers, Bernadette[UCL] Dahan, Karin[UCL] (2006) American journal of ophthalmology — Vol. 142, no. 6, p. 1089-92 (2006)
    • Journal article
    Evolution of communication abilities after cochlear implantation in prelingually deaf children
    Gérard, Jean-Marc[UCL] Deggouj, Naima Hupin, Cloé[UCL] Buisson, Anne-Laure[UCL] Monteyne, Veronique[UCL] Lavis, C.[UCL] Dahan, Karin[UCL] Gersdorff, Michel (2010) International Journal of Pediatric Otorhinolaryngology — Vol. 74, no. 6, p. 642-648 (2010)
    • Speech
    Syndrome de Gitelman et protéinurie glomérulaire: à propos d'une association atypique
    Demoulin, Nathalie[UCL] Cosyns, Jean-Pierre[UCL] Cornet, C. Godefroid, Nathalie[UCL] Pirson, Yves[UCL] Jadoul, Michel[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2010) 12e Réunion commune de la Société de Néphrologie (SN) et de la Société Francophone de Dialyse (SFD) — (Belgium) Brussels
    • Journal article
    [Secondary hemochromatosis - Response]
    Buysschaert, Martin[UCL] Dahan, Karin[UCL] Paris, Isabelle (1999) Acta Clinica Belgica (Multilingual Edition) — Vol. 54, no. 3, p. 173-174 (1999)
    • Journal article
    A homozygous mutation in INVS causing juvenile nephronophthisis with abnormal reactivity of the Wnt/beta-catenin pathway
    Bellavia, Salvatore[UCL] Dahan, Karin[UCL] Terryn, Sara[UCL] Cosyns, Jean-Pierre[UCL] Devuyst, Olivier[UCL] Pirson, Yves[UCL] (2010) Nephrology, Dialysis, Transplantation — Vol. 25, no. 12, p. 4097-4102 (2010)

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