Works matching AU Masurel‐Paulet, Alice

Results: 9
    1

    The molecular and phenotypic spectrum of IQSEC2-related epilepsy.

    Published in:
    Epilepsia (Series 4), 2016, v. 57, n. 11, p. 1858, doi. 10.1111/epi.13560
    By:
    • Zerem, Ayelet;
    • Haginoya, Kazuhiro;
    • Lev, Dorit;
    • Blumkin, Lubov;
    • Kivity, Sara;
    • Linder, Ilan;
    • Shoubridge, Cheryl;
    • Palmer, Elizabeth Emma;
    • Field, Michael;
    • Boyle, Jackie;
    • Chitayat, David;
    • Gaillard, William D.;
    • Kossoff, Eric H.;
    • Willems, Marjolaine;
    • Geneviève, David;
    • Tran-Mau-Them, Frederic;
    • Epstein, Orna;
    • Heyman, Eli;
    • Dugan, Sarah;
    • Masurel-Paulet, Alice
    Publication type:
    Article
    2

    Changing facial phenotype in Cohen syndrome: towards clues for an earlier diagnosis.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 7, p. 736, doi. 10.1038/ejhg.2012.251
    By:
    • El Chehadeh-Djebbar, Salima;
    • Blair, Edward;
    • Holder-Espinasse, Muriel;
    • Moncla, Anne;
    • Frances, Anne-Marie;
    • Rio, Marlène;
    • Debray, François-Guillaume;
    • Rump, Patrick;
    • Masurel-Paulet, Alice;
    • Gigot, Nadège;
    • Callier, Patrick;
    • Duplomb, Laurence;
    • Aral, Bernard;
    • Huet, Frédéric;
    • Thauvin-Robinet, Christel;
    • Faivre, Laurence
    Publication type:
    Article
    3

    12p13.33 microdeletion including ELKS/ERC1, a new locus associated with childhood apraxia of speech.

    Published in:
    European Journal of Human Genetics, 2013, v. 21, n. 1, p. 82, doi. 10.1038/ejhg.2012.116
    By:
    • Thevenon, Julien;
    • Callier, Patrick;
    • Andrieux, Joris;
    • Delobel, Bruno;
    • David, Albert;
    • Sukno, Sylvie;
    • Minot, Delphine;
    • Mosca Anne, Laure;
    • Marle, Nathalie;
    • Sanlaville, Damien;
    • Bonnet, Marlène;
    • Masurel-Paulet, Alice;
    • Levy, Fabienne;
    • Gaunt, Lorraine;
    • Farrell, Sandra;
    • Le Caignec, Cédric;
    • Toutain, Annick;
    • Carmignac, Virginie;
    • Mugneret, Francine;
    • Clayton-Smith, Jill
    Publication type:
    Article
    4

    Genomic deletions of OFD1 account for 23% of oral-facial-digital type 1 syndrome after negative DNA sequencing.

    Published in:
    Human Mutation, 2009, v. 30, n. 2, p. E320, doi. 10.1002/humu.20888
    By:
    • Thauvin-Robinet, Christel;
    • Franco, Brunella;
    • Saugier-Veber, Pascale;
    • Aral, Bernard;
    • Gigot, Nadège;
    • Donzel, Anne;
    • Van Maldergem, Lionel;
    • Bieth, Eric;
    • Layet, Valérie;
    • Mathieu, Michèle;
    • Teebi, Ahmad;
    • Lespinasse, James;
    • Callier, Patrick;
    • Mugneret, Francine;
    • Masurel-Paulet, Alice;
    • Gautier, Elodie;
    • Huet, Frédéric;
    • Teyssier, Jean-Raymond;
    • Tosi, Mario;
    • Frébourg, Thierry
    Publication type:
    Article
    5

    A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 8, p. 2103, doi. 10.1002/ajmg.a.37765
    By:
    • Masurel‐Paulet, Alice;
    • Piton, Amélie;
    • Chancenotte, Sophie;
    • Redin, Claire;
    • Thauvin‐Robinet, Christel;
    • Henrenger, Yvan;
    • Minot, Delphine;
    • Creppy, Audrey;
    • Ruffier‐Bourdet, Marie;
    • Thevenon, Julien;
    • Kuentz, Paul;
    • Lehalle, Daphné;
    • Curie, Aurore;
    • Blanchard, Gaelle;
    • Ghosn, Ezzat;
    • Bonnet, Marlene;
    • Archimbaud‐Devilliers, Mélanie;
    • Huet, Frédéric;
    • Perret, Odile;
    • Philip, Nicole
    Publication type:
    Article
    6

    Further delineation of eye manifestations in homozygous 15q13.3 microdeletions including TRPM1: A differential diagnosis of ceroid lipofuscinosis.

    Published in:
    American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 6, p. 1537, doi. 10.1002/ajmg.a.36471
    By:
    • Masurel‐Paulet, Alice;
    • Drumare, Isabelle;
    • Holder, Muriel;
    • Cuisset, Jean‐Marie;
    • Vallée, Louis;
    • Defoort, Sabine;
    • Bourgois, Béatrice;
    • Pernes, Philippe;
    • Cuvellier, Jean‐Christophe;
    • Huet, Frédéric;
    • Chehadeh, Salima El;
    • Thevenon, Julien;
    • Callier, Patrick;
    • Thauvin, Christel;
    • Faivre, Laurence;
    • Andrieux, Joris
    Publication type:
    Article
    7

    Expanding the clinical phenotype of patients with a ZDHHC9 mutation.

    Published in:
    American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 3, p. 789, doi. 10.1002/ajmg.a.36348
    By:
    • Masurel‐Paulet, Alice;
    • Kalscheuer, Vera M.;
    • Lebrun, Nicolas;
    • Hu, Hao;
    • Levy, Fabienne;
    • Thauvin‐Robinet, Christel;
    • Darmency‐Stamboul, Véronique;
    • El Chehadeh, Salima;
    • Thevenon, Julien;
    • Chancenotte, Sophie;
    • Ruffier‐Bourdet, Marie;
    • Bonnet, Marlène;
    • Pinoit, Jean‐Michel;
    • Huet, Frédéric;
    • Desportes, Vincent;
    • Chelly, Jamel;
    • Faivre, Laurence
    Publication type:
    Article
    8

    Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy.

    Published in:
    Annals of Clinical & Translational Neurology, 2017, v. 4, n. 1, p. 26, doi. 10.1002/acn3.372
    By:
    • Kambouris, Marios;
    • Thevenon, Julien;
    • Soldatos, Ariane;
    • Cox, Allison;
    • Stephen, Joshi;
    • Ben‐Omran, Tawfeg;
    • Al‐Sarraj, Yasser;
    • Boulos, Hala;
    • Bone, William;
    • Mullikin, James C.;
    • Masurel‐Paulet, Alice;
    • St‐Onge, Judith;
    • Dufford, Yannis;
    • Chantegret, Corrine;
    • Thauvin‐Robinet, Christel;
    • Al‐Alami, Jamil;
    • Faivre, Laurence;
    • Riviere, Jean Baptiste;
    • Gahl, William A.;
    • Bassuk, Alexander G.
    Publication type:
    Article
    9