Found: 4

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  • Biallelic loss‐of‐function variants in RBL2 in siblings with a neurodevelopmental disorder.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 3, p. 390, doi. 10.1002/acn3.50992
    By:
    • Brunet, Theresa;
    • Radivojkov‐Blagojevic, Milena;
    • Lichtner, Peter;
    • Kraus, Verena;
    • Meitinger, Thomas;
    • Wagner, Matias
    Publication type:
    Article

  • Longitudinally Extensive Optic Neuritis in Pediatric Patients.

    Published in:
    Journal of Child Neurology, 2015, v. 30, n. 1, p. 120, doi. 10.1177/0883073813520500
    By:
    • Graves, Jennifer;
    • Kraus, Verena;
    • Soares, Bruno P.;
    • Hess, Christopher P.;
    • Waubant, Emmanuelle
    Publication type:
    Article

  • Atypical Cases of Scleroderma en Coup de Sabre.

    Published in:
    Journal of Child Neurology, 2014, v. 29, n. 5, p. 698, doi. 10.1177/0883073813520494
    By:
    • Kraus, Verena;
    • Lawson, Erica F.;
    • Scheven, Emily von;
    • Tihan, Tarik;
    • Garza, Judith;
    • Nathan, Rani G.;
    • Cordoro, Kelly M.;
    • Waubant, Emmanuelle
    Publication type:
    Article

  • Pediatric Herpes Simplex Virus Encephalitis: A Retrospective Multicenter Experience.

    Published in:
    Journal of Child Neurology, 2013, v. 28, n. 3, p. 321, doi. 10.1177/0883073812471428
    By:
    • Schleede, Lena;
    • Bueter, Wolfgang;
    • Baumgartner-Sigl, Sara;
    • Opladen, Thomas;
    • Weigt-Usinger, Katharina;
    • Stephan, Susanne;
    • Smitka, Martin;
    • Leiz, Steffen;
    • Kaiser, Olaf;
    • Kraus, Verena;
    • van Baalen, Andreas;
    • Skopnik, Heino;
    • Hartmann, Hans;
    • Rostasy, Kevin;
    • Lücke, Thomas;
    • Schara, Ulrike;
    • Häusler, Martin
    Publication type:
    Article