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1. • Article de périodique

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   Délétion du bras long du chromosome 18, hypothyroïdie primaire, anémie de Biermer et hypogammaglobulinémie de type IgM.

   Henrot, B. Ninane, J. Mercenier, C.[UCL] Vermylen, Christiane[UCL] Dumoulin, Christine[UCL] Cornu, Guy[UCL] Malvaux, Paul[UCL] (1989) Archives françaises de pédiatrie — Vol. 46, no. 10, p. 729-732 (1989)
2. • Article de périodique

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   Leiomyoma of the suprarenal gland in a child with ataxia-telangiectasia.

   Mouchet, F Ninane, J. Gosseye, Serge[UCL] Dumoulin, Christine[UCL] Bonnier, Christine Evrard, Philippe[UCL] Vermylen, Christiane[UCL] Scheiff, Jean-Marie[UCL] Cornu, Guy[UCL] (1991) Pediatric hematology and oncology — Vol. 8, no. 3, p. 235-41 (1991)
3. • Article de périodique

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   Réanimation postopératoire et tratiement diététique au long cours dans un cas de résection étendue de l'intestin chez l'enfant

   Otte, Jean-Bernard[UCL] Fiasse, René[UCL] Cornu, Guy[UCL] Dumoulin, Christine[UCL] (1974) Acta paediatrica Belgica — Vol. 28, no. 1, p. 40-8 (1974)
4. • Article de périodique

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   Implications psychologiques des études familiales en biologie moléculaire. Un exemple: la myopathie de Duchenne.

   Hayez, Jean-Yves[UCL] Dumoulin, Christine[UCL] (1989) Journal de génétique humaine — Vol. 37, no. 1, p. 29-38 (1989)
5. • Article de périodique

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   The nuclear factor kappaB-activator gene PLEKHG5 is mutated in a form of autosomal recessive lower motor neuron disease with childhood onset

   Maystadt, Isabelle[UCL] Rezsohazy, René[UCL] Barkats, Martine Duque, Sandra Vannuffel, Pascal Remacle, Sophie[UCL] Lambert, Barbara[UCL] Najimi, Mustapha[UCL] Sokal, Etienne[UCL] Munnich, Arnold Viollet, Louis Dumoulin, Christine[UCL] (2007) American Journal of Human Genetics — Vol. 81, no. 1, p. 67-76 (2007)
6. • Article de périodique

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   Autosomal-dominant chronic interstitial nephritis with early hyperuricemia.

   Pirson, Yves[UCL] Loute, G. Cosyns, Jean-Pierre[UCL] Dahan, Karin[UCL] Dumoulin, Christine[UCL] (2000) Advances in nephrology from the Necker Hospital — Vol. 30, p. 357-369 (2000)
7. • Article de périodique

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   CF gene and cystic fibrosis transmembrane conductance regulator expression in autosomal dominant polycystic kidney disease.

   Persu, Alexandre[UCL] Devuyst, Olivier[UCL] Lannoy, N. Materne, R Brosnahan, G Gabow, P A Pirson, Yves[UCL] Dumoulin, Christine[UCL] (2000) Journal of the American Society of Nephrology : JASN — Vol. 11, no. 12, p. 2285-96 (2000)
8. • Article de périodique

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   Autosomal dominant polycystic kidney disease in the first year of life. Report of a case with no family history.

   Stalens, J P Sokal, Etienne[UCL] Walon, C. Dumoulin, Christine[UCL] Clapuyt, Philippe[UCL] Wese, François-Xavier[UCL] (1993) Acta urologica Belgica — Vol. 61, no. 4, p. 25-8 (1993)
9. • Article de périodique

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   Hypodiploidy is a major prognostic factor in multiple myeloma.

   Smadja, N V Bastard, C Brigaudeau, C Leroux, D Fruchart, C Groupe Français de Cytogénétique Hématologique Michaux, Lucienne[UCL] Libouton, J.M.[UCL] Dumoulin, Christine[UCL] Scheiff, Jean-Marie[UCL] Deneys, Véronique[UCL] Ferrant, Augustin[UCL] (2001) Blood — Vol. 98, no.7, p. 2229-2238 (2001)
10. • Article de périodique

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    Very-long-chain acyl-CoA dehydrogenase deficiency in two siblings : good evolution after prenatal diagnosis and prompt management

    Sluysmans, Thierry[UCL] Tuerlinckx, David[UCL] Hubinont, Corinne[UCL] Dumoulin, Christine[UCL] Brivet, M. Vianey-Saban, C. (1997) Mini Acta — Vol. 29, no.3, p. 183-188 (1997)
11. • Article de périodique

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    Eye Anomalies and Ocular Motor Disorders in the Oral-facial-digital Syndrome Type-ii

    Spiritus, Micheline[UCL] Verellen, Gaston[UCL] Waterschoot, MP. Bottu, J. Lepolain, D. Dumoulin, Christine[UCL] (1987) Neuro-Ophthalmology — Vol. 7, no. 4, p. 223-226 (1987)
12. • Article de périodique

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    Mutations in GDAP1 - Autosomal recessive CMT with demyelination and axonopathy

    Nelis, E. Erdem, S Van den Bergh, Peter[UCL] Belpaire-Dethiou, MC[UCL] Ceuterick, C. Van Gerwen, V Cuesta, A Pedrola, L Palau, F Gabreels-Festen, AAWM Dumoulin, Christine[UCL] Tan, E Demirci, M Van Broeckhoven, C De Jonghe, P. Topaloglu, H Timmerman, V (2002) Neurology — Vol. 59, no. 12, p. 1865-1872 (2002)
13. • Communication

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    Difficult genetic counseling in a family with pathogenic BRCA2 mutation.

    Ingargiola, II Dahan, Karin[UCL] Smaers, M Van Cangh, Paul[UCL] Dumoulin, Christine[UCL] (2001) —
14. • Article de périodique

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    Oral-facial-digital Syndrome Type-i in a Newborn Male

    Gillerot, Y. Heimann, M. Fourneau, C. Dumoulin, Christine[UCL] Vanmaldergem, L. (1993) American Journal of Medical Genetics — Vol. 46, no. 3, p. 335-338 (1993)
15. • Article de périodique

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    S-100 Protein in Amniotic-fluid of Anencephalic Fetuses

    Sindic, Christian[UCL] Freund, M. Vanregemorter, N. Dumoulin, Christine[UCL] Masson, PL. (1984) Prenatal Diagnosis — Vol. 4, no. 4, p. 297-302 (1984)
16. • Article de périodique

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    Le lymphangiome kystique du mésentère. Problèmes thérapeutiques posés par un cas compliqué d'ascite chyleuse et associé à des troubles électrolytiques majeurs

    Otte, Jean-Bernard[UCL] Cornu, Guy[UCL] Cosyns, Jean-Pierre[UCL] Dumoulin, Christine[UCL] Claus, D. (1974) Acta paediatrica Belgica — Vol. 28, no. 2, p. 103-21 (1974)
17. • Article de périodique

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    Familial adenomatous polyposis associated with multiple adrenal adenomas in a patient with a rare 3' APC mutation.

    Kartheuser, Alex[UCL] Walon, Corinne[UCL] West, Sarah Breukel, Cor Detry, Roger[UCL] Gribomont, Anne-Catherine[UCL] Hamzehloei, Tayebeh Hoang, Pierre[UCL] Maiter, Dominique[UCL] Pringot, Jacques[UCL] Rahier, Jacques[UCL] Khan, Meera P. Curtis, Ann Burn, John Fodde, Riccardo Dumoulin, Christine[UCL] (1999) Journal of Medical Genetics : an international peer-reviewed journal for health professionals and researchers in all areas of genetics — Vol. 36, no. 1, p. 65-67 (1999)
18. • Article de périodique

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    Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.

    Ghassibé, Michella[UCL] Revencu, Nicole[UCL] Bayet, Bénédicte[UCL] Gillerot, Yves[UCL] Vanwijck, Romain[UCL] Dumoulin, Christine[UCL] Vikkula, Miikka[UCL] (2004) Journal of Medical Genetics — Vol. 41, no. 2, p. 1-5 (2004)
19. • Article de périodique

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    No Significant Effect of Monosomy for Distal 21q22.3 On the Down-syndrome Phenotype in Mirror Duplications of Chromosome-21

    Pangalos, C. Theophile, D. Sinet, PM. Marks, A. Stambouliehabazis, D. Chettouh, Z. Prieur, M. Dumoulin, Christine[UCL] Rethore, MO. Lejeune, J. Delabar, JM. (1992) American Journal of Human Genetics — Vol. 51, no. 6, p. 1240-1250 (1992)
20. • Communication

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    Mutations in the UMOD gene lead to abnormal expression of uromodulin in familial juvenile hyperuricemic nephropathy.

    Devuyst, Olivier[UCL] Dahan, Karin[UCL] Pirson, Yves[UCL] Cosyns, Jean-Pierre[UCL] Dumoulin, Christine[UCL] (2003) 36th Annual Meeting of the American-Society-of-Nephrology — SAN DIEGO (California)
21. • Communication

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    Phenotype and differential diagnosis of a neonatal Marfan syndrome due to a new FBN-1 exon 25 mutation

    Revencu, Nicole[UCL] Verellen, Gaston[UCL] Quenum, G Thim, VVS Collard, L De Paepe, A. Dumoulin, Christine[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
22. • Communication

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    Carney triad in a patient with balanced translocation t(1;19)(p11-13;p11-12).

    Thim, VVS Sibille, Catherine[UCL] Dumoulin, Christine[UCL] (2002) European-Society-of-Human-Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics — STRASBOURG (France)
23. • Article de périodique

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    [Study of the Sensitivity To Mutagens and of the Repair Process On Lymphocytes From the Werners Syndrome]

    Deknudt, G. Dumoulin, Christine[UCL] Léonard, Alain[UCL] (1985) Societe de Biologie et de Ses Filiales. Comptes Rendus des Seances — Vol. 179, no. 4, p. 518-521 (1985)
24. • Communication

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    Homozygosity for facioscapulohumeral muscular dystrophy (FSHD) gene

    Canki-Klain, N Zagar, M Lannoy, N. Dumoulin, Christine[UCL] Zurak, N (2001) —
25. • Communication

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    Comparison of two culture media for routine conventional cytogenetic analysis in multiple myeloma and MGUS.

    Samani, KK Ferrant, Augustin[UCL] Michaux, Lucienne[UCL] Libouton, Jeanne-Marie[UCL] Dumoulin, Christine[UCL] (2000) —

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