Works matching IS 03405354 AND DT 2012 AND VI 259 AND IP 3


Results: 35
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    SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease.

    Published in:
    Journal of Neurology, 2012, v. 259, n. 3, p. 515, doi. 10.1007/s00415-011-6213-8
    By:
    • Fischer, Carina;
    • Trajanoski, Slave;
    • Papić, Lea;
    • Windpassinger, Christian;
    • Bernert, Günther;
    • Freilinger, Michael;
    • Schabhüttl, Maria;
    • Arslan-Kirchner, Mine;
    • Javaher-Haghighi, Poupak;
    • Plecko, Barbara;
    • Senderek, Jan;
    • Rauscher, Christian;
    • Löscher, Wolfgang;
    • Pieber, Thomas;
    • Janecke, Andreas;
    • Auer-Grumbach, Michaela
    Publication type:
    Article
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    A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome.

    Published in:
    Journal of Neurology, 2012, v. 259, n. 3, p. 474, doi. 10.1007/s00415-011-6204-9
    By:
    • Chaouch, Amina;
    • Müller, Juliane;
    • Guergueltcheva, Velina;
    • Dusl, Marina;
    • Schara, Ulrike;
    • Rakocević-Stojanović, Vidosava;
    • Lindberg, Christopher;
    • Scola, Rosana;
    • Werneck, Lineu;
    • Colomer, Jaume;
    • Nascimento, Andres;
    • Vilchez, Juan;
    • Muelas, Nuria;
    • Argov, Zohar;
    • Abicht, Angela;
    • Lochmüller, Hanns
    Publication type:
    Article
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    Leonid Ivanovich Omorokov (1881-1971).

    Published in:
    Journal of Neurology, 2012, v. 259, n. 3, p. 595, doi. 10.1007/s00415-011-6220-9
    By:
    • Bogdanov, Enver;
    • Mukhamedzyanov, Ravil;
    • Sozinov, Alexey;
    • Vilensky, Joel
    Publication type:
    Article
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