Works matching AU Gouider-Khouja, Neziha

Results: 9
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    Eye movements in parkinsonian syndromes.

    Published in:
    Annals of Neurology, 1994, v. 35, n. 4, p. 420, doi. 10.1002/ana.410350408
    By:
    • Vidailhet, Marie;
    • Rivaud, Sophie;
    • Gouider-Khouja, Neziha;
    • Pillon, Bernard;
    • Bonnet, Anne-Marie;
    • Gaymard, Bertrand;
    • Agid, Yves;
    • Pierrot-Deseilligny, Charles
    Publication type:
    Article
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    Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.

    Published in:
    Movement Disorders, 2006, v. 21, n. 8, p. 1102, doi. 10.1002/mds.20886
    By:
    • Tomiyama, Hiroyuki;
    • Li, Yuanzhe;
    • Funayama, Manabu;
    • Hasegawa, Kazuko;
    • Yoshino, Hiroyo;
    • Kubo, Shin-Ichiro;
    • Sato, Kenichi;
    • Hattori, Tatsuya;
    • Lu, Chin-Song;
    • Inzelberg, Rivka;
    • Djaldetti, Ruth;
    • Melamed, Eldad;
    • Amouri, Rim;
    • Gouider-Khouja, Neziha;
    • Hentati, Faycal;
    • Hatano, Yasuko;
    • Wang, Mei;
    • Imamichi, Yoko;
    • Mizoguchi, Koichi;
    • Miyajima, Hiroaki
    Publication type:
    Article
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    Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 1, doi. 10.1186/1750-1172-9-72
    By:
    • Romani, Marta;
    • Micalizzi, Alessia;
    • Kraoua, Ichraf;
    • Dotti, Maria Teresa;
    • Cavallin, Mara;
    • Sztriha, László;
    • Ruta, Rosario;
    • Mancini, Francesca;
    • Mazza, Tommaso;
    • Castellana, Stefano;
    • Hanene, Benrhouma;
    • Carluccio, Maria Alessandra;
    • Darra, Francesca;
    • Máté, Adrienn;
    • Zimmermann, Alíz;
    • Gouider-Khouja, Neziha;
    • Valente, Enza Maria
    Publication type:
    Article
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