Výsledky vyhledávání - Matthew Sweney

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  1. 1
    The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond

    The Expanding Spectrum of Neurological Phenotypes in Children With ATP1A3 Mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and Beyond Autor Matthew Sweney, Tara Newcomb, Kathryn J. Swoboda

    Vydáno 2014
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  2. 2
    Disparities in Pediatric Epilepsy Remission Are Associated With Race and Ethnicity

    Disparities in Pediatric Epilepsy Remission Are Associated With Race and Ethnicity Autor Celestine H. Yeung Gregerson, Amanda V. Bakian, Jacob Wilkes, Andrew J. Knighton, Flory L. Nkoy, Matthew Sweney, Francis Filloux, Joshua L. Bonkowsky

    Vydáno 2019
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  3. 3
    Mobile Software as a Medical Device (SaMD) for the Treatment of Epilepsy: Development of Digital Therapeutics Comprising Behavioral and Music-Based Interventions for Neurological Disorders

    Mobile Software as a Medical Device (SaMD) for the Treatment of Epilepsy: Development of Digital Therapeutics Comprising Behavioral and Music-Based Interventions for Neurological D... Autor Pegah Afra, Carol S. Bruggers, Matthew Sweney, Lilly Fagatele, Fareeha Alavi, Michael J. Greenwald, Merodean Huntsman, Khanhly Nguyen, Jeremiah K. Jones, David Shantz, Grzegorz Bułaj

    Vydáno 2018
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  4. 4
    Research conference summary from the 2014 International Task Force on <i>ATP1A3</i> -Related Disorders

    Research conference summary from the 2014 International Task Force on <i>ATP1A3</i> -Related Disorders Autor Hendrik Rosewich, Matthew Sweney, Suzanne D. DeBrosse, Kevin C. Ess, Laurie J. Ozelius, Eva Andermann, Frédérick Andermann, Gene Andrasco, Alice Belgrade, Allison Brashear, Sharon Ciccodicola, Lynn Egan, Alfred L. George, Aga Lewelt, Joshua Magelby, Mario Merida, Tara Newcomb, Vicky Platt, D. Poncelin, Sandra P. Reyna, Masayuki Sasaki, Márcio Sotero de Menezes, Kathleen J. Sweadner, Louis Viollet, Mary L. Zupanc, Kenneth Silver, Kathryn J. Swoboda

    Vydáno 2017
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  5. 5
    Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

    Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry Autor Louis Viollet, Gustavo Glusman, Kelley J. Murphy, Tara Newcomb, Sandra P. Reyna, Matthew Sweney, B.E. Nelson, Frédérick Andermann, Eva Andermann, Gyula Acsádi, Richard L. Barbano, Candida Brown, Mary E. Brunkow, Harry T. Chugani, Sarah Cheyette, Abigail Collins, Suzanne D. DeBrosse, David J. Galas, Jennifer Friedman, Lee Hood, Chad Huff, Lynn B. Jorde, Mary D. King, Bernie LaSalle, Richard J. Leventer, Aga Lewelt, Mylynda Massart, Mario Merida, Louis J. Ptác̆ek, Jared C. Roach, Robert S. Rust, Francis Renault, Terry D. Sanger, Márcio A Sotero de Menezes, Rachel B. Tennyson, Peter Uldall, Yue Zhang, Mary L. Zupanc, Winnie Xin, Kenneth Silver, Kathryn J. Swoboda

    Vydáno 2015
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  6. 6
    Guidelines for Specialized Epilepsy Centers

    Guidelines for Specialized Epilepsy Centers Autor Fred A. Lado, Stephanie M. Ahrens, Ellen Riker, Carrie R. Muh, R. Mark Richardson, Johanna M. Gray, Barbara Small, Sandra Zelman Lewis, Thomas J. Schofield, Dave Clarke, Jennifer L. Hopp, Roland R. Lee, Jay A. Salpekar, Susan T. Arnold, Jocelyn F. Bautista, Ramon Edmundo D. Bautista, Stephen Chan, Sheri Cotterman-Hart, Dawn Deines, Breanne Fisher, Cecile Gayanilo, Randa Jarrar, Genesee Kayton, Kathryn Lalor, Kerri Neville, Juan G. Ochoa, Madona Plueger, Steven M. Rothman, Jason M. Schwalb, Olga Selioutski, Laureen Vassil, Susan Agostini, Rosario DeLeon, Robert E. Gross, Dylan Isaacs, Steve Kahanic, Chris Morrison, Lilian Omburo, Holly Paauwe, Annapurna Poduri, Kate Recore, Amy Reynolds, R. Riel-Romero, Lisa G. Riley, Evan Sandok, Saurabh R. Sinha, Matthew Sweney

    Vydáno 2024
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  7. 7
    De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

    De novo mutations in ATP1A3 cause alternating hemiplegia of childhood Autor Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries, Francesco Danilo Tiziano, Bertrand Fontaine, Sophie Nicole, Sinéad B. Heavin, Eleni Panagiotakaki, Sophie Nicole, Fiorella Gurrieri, Giovanni Neri, Boukje de Vries, Stephany C Koelewijn, Jessica T. Kamphorst, Marije A. Geilenkirchen, Nadine Pelzer, Laura Laan, Joost Haan, Michel D. Ferrari, Arn van den Maagdenberg, Claudio Zucca, Maria Teresa Bassi, F Franchini, Rosaria Vavassori, Melania Giannotta, Giuseppe Gobbi, Tiziana Granata, Nardo Nardocci, Elisa De Grandis, E. Veneselli, Michela Stagnaro, Fiorella Gurrieri, Giovanni Neri, Federico Vigevano, Eleni Panagiotakaki, Claudia Oechsler, Alexis Arzimanoglou, Sophie Nicole, Melania Giannotta, Giuseppe Gobbi, Miriam Ninan, Brian Neville, Friedrich Ebinger, Carmen Fons, Jaume Campistol, David Kemlink, Soňa Nevšímalová, Laura Laan, Cacha Peeters‐Scholte, Arn van den Maagdenberg, Paul Casaer, Giorgio Casari, Guenter Sange, Georg Spiel, Filippo Martinelli Boneschi, Claudio Zucca, Maria Teresa Bassi, Tsveta Schyns, Francis P. Crawley, Dominique Poncelin, Rosaria Vavassori, Stefania Fiori, Emanuela Abiusi, Lorena Di Pietro, Matthew Sweney, Tara Newcomb, Louis Viollet, Chad D. Huff, Lynn B. Jorde, Sandra P. Reyna, Kelley J. Murphy, Kevin V. Shianna, Curtis Gumbs, Latasha Little, Kenneth Silver, Louis J. Ptáček, Joost Haan, Michel D. Ferrari, Ann Bye, Geoffrey Herkes, Charlotte M Whitelaw, David Webb, Bryan J. Lynch, Peter Uldall, Mary D. King, Ingrid E. Scheffer, Giovanni Neri, Alexis Arzimanoglou, Arn M. J. M. van den Maagdenberg, Sanjay M. Sisodiya, Mohamad A. Mikati, David B. Goldstein

    Vydáno 2012
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