Works matching IS 24709239 AND DT 2019 AND VI 4 AND IP 3

Results: 17
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    Possible precision medicine implications from genetic testing using combined detection of sequence and intragenic copy number variants in a large cohort with childhood epilepsy.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 3, p. 397, doi. 10.1002/epi4.12348
    By:
    • Truty, Rebecca;
    • Patil, Nila;
    • Sankar, Raman;
    • Sullivan, Joseph;
    • Millichap, John;
    • Carvill, Gemma;
    • Entezam, Ali;
    • Esplin, Edward D.;
    • Fuller, Amy;
    • Hogue, Michelle;
    • Johnson, Britt;
    • Khouzam, Amirah;
    • Kobayashi, Yuya;
    • Lewis, Rachel;
    • Nykamp, Keith;
    • Riethmaier, Darlene;
    • Westbrook, Jody;
    • Zeman, Michelle;
    • Nussbaum, Robert L.;
    • Aradhya, Swaroop
    Publication type:
    Article
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    Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 3, p. 504, doi. 10.1002/epi4.12350
    By:
    • Ware, Tyson L.;
    • Huskins, Shannon R.;
    • Grinton, Bronwyn E.;
    • Liu, Yu‐Chi;
    • Bennett, Mark F.;
    • Harvey, Michael;
    • McMahon, Jacinta;
    • Andreopoulos‐Malikotsinas, Danae;
    • Bahlo, Melanie;
    • Howell, Katherine B.;
    • Hildebrand, Michael S.;
    • Damiano, John A.;
    • Rosenfeld, Alexander;
    • Mackay, Mark T.;
    • Mandelstam, Simone;
    • Leventer, Richard J.;
    • Harvey, A. Simon;
    • Freeman, Jeremy L.;
    • Scheffer, Ingrid E.;
    • Jones, Dean L.
    Publication type:
    Article
    7

    Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 3, p. 420, doi. 10.1002/epi4.12349
    By:
    • Silvennoinen, Katri;
    • Lange, Nikola;
    • Zagaglia, Sara;
    • Balestrini, Simona;
    • Androsova, Ganna;
    • Wassenaar, Merel;
    • Auce, Pauls;
    • Avbersek, Andreja;
    • Becker, Felicitas;
    • Berghuis, Bianca;
    • Campbell, Ellen;
    • Coppola, Antonietta;
    • Francis, Ben;
    • Wolking, Stefan;
    • Cavalleri, Gianpiero L.;
    • Craig, John;
    • Delanty, Norman;
    • Johnson, Michael R.;
    • Koeleman, Bobby P. C.;
    • Kunz, Wolfram S.
    Publication type:
    Article
    8

    A novel homozygous KCNQ3 loss‐of‐function variant causes non‐syndromic intellectual disability and neonatal‐onset pharmacodependent epilepsy.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 3, p. 464, doi. 10.1002/epi4.12353
    By:
    • Lauritano, Anna;
    • Moutton, Sebastien;
    • Longobardi, Elena;
    • Tran Mau‐Them, Frédéric;
    • Laudati, Giusy;
    • Nappi, Piera;
    • Soldovieri, Maria Virginia;
    • Ambrosino, Paolo;
    • Cataldi, Mauro;
    • Jouan, Thibaud;
    • Lehalle, Daphné;
    • Maurey, Hélène;
    • Philippe, Christophe;
    • Miceli, Francesco;
    • Vitobello, Antonio;
    • Taglialatela, Maurizio
    Publication type:
    Article
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    10

    Changes in drug load during lacosamide combination therapy: A noninterventional, observational study in German and Austrian clinical practice.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 3, p. 409, doi. 10.1002/epi4.12346
    By:
    • Reinhardt, Fritjof;
    • Weber, Yvonne G.;
    • Mayer, Thomas;
    • Luef, Gerhard;
    • Joeres, Lars;
    • Tennigkeit, Frank;
    • Dedeken, Peter;
    • De Backer, Marc;
    • Hellot, Scarlett;
    • Lauterbach, Thomas;
    • Webers, Tanja;
    • Arnold, Stephan;
    • Asenbaum‐Nan, Susanne;
    • Behrens, Stephan;
    • Bethke, Florian;
    • Bös, Monika;
    • Bongartz, Ulrike;
    • Christopher, Angelika;
    • Geber, Christian;
    • Halbgewachs, Frank
    Publication type:
    Article
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    Issue Information.

    Published in:
    Epilepsia Open, 2019, v. 4, n. 3, p. 363, doi. 10.1002/epi4.12245
    Publication type:
    Article