SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Robert Wilcox, Ingrid Brænne, Norbert Brüggemann, Susen Winkler, Karin Wiegers, Lars Bertram, Tim Anderson, Katja Lohmann, Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only, Journal of Neurology, 2015, 262, 1, 187

    CrossRef

  2. 2
    B. Balint, K. P. Bhatia, Isolated and combined dystonia syndromes – an update on new genes and their phenotypes, European Journal of Neurology, 2015, 22, 4
  3. 3
    Alex R. Paciorkowski, Sharon S. McDaniel, Laura A. Jansen, Hannah Tully, Emily Tuttle, Dalia H. Ghoneim, Srinivasan Tupal, Sonya A. Gunter, Valeria Vasta, Qing Zhang, Thao Tran, Yi B. Liu, Laurie J. Ozelius, Allison Brashear, Kathleen J. Sweadner, William B. Dobyns, Sihoun Hahn, Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly, Epilepsia, 2015, 56, 3
  4. 4
    Susanne A. Schneider, Movement Disorders, 2015,

    CrossRef

  5. 5
    Emmanuel Roze, Aurélie Méneret, Marie Vidailhet, Movement Disorders, 2015,

    CrossRef

  6. 6
    Hendrik Rosewich, Martina Baethmann, Andreas Ohlenbusch, Jutta Gärtner, Knut Brockmann, A novel ATP1A3 mutation with unique clinical presentation, Journal of the Neurological Sciences, 2014, 341, 1-2, 133

    CrossRef

  7. 7
    Karl M. Weigand, Muriël Messchaert, Herman G.P. Swarts, Frans G.M. Russel, Jan B. Koenderink, Alternating Hemiplegia of Childhood mutations have a differential effect on Na+,K+-ATPase activity and ouabain binding, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2014, 1842, 7, 1010

    CrossRef

  8. 8
    Marta Vila-Pueyo, Roser Pons, Miquel Raspall-Chaure, Anna Marcé-Grau, Oriel Carreño, Cèlia Sintas, Bru Cormand, Mercè Pineda-Marfà, Alfons Macaya, Clinical and genetic analysis in alternating hemiplegia of childhood: Ten new patients from Southern Europe, Journal of the Neurological Sciences, 2014, 344, 1-2, 37

    CrossRef

  9. 9
    Cyrus Boelman, Ana Marissa Lagman-Bartolome, Daune L. MacGregor, Jane McCabe, Willam J. Logan, Berge A. Minassian, Identical ATP1A3 Mutation Causes Alternating Hemiplegia of Childhood and Rapid-Onset Dystonia Parkinsonism Phenotypes, Pediatric Neurology, 2014, 51, 6, 850

    CrossRef