SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Keiko Shimojima, Akihisa Okumura, Mitsuru Ikeno, Akira Nishimura, Akira Saito, Hirotomo Saitsu, Naomichi Matsumoto, Toshiyuki Yamamoto, A de novo TUBB4A mutation in a patient with hypomyelination mimicking Pelizaeus–Merzbacher disease, Brain and Development, 2014,

    CrossRef

  2. 2
    Y. Saillour, L. Broix, E. Bruel-Jungerman, N. Lebrun, G. Muraca, J. Rucci, K. Poirier, R. Belvindrah, F. Francis, J. Chelly, Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown, Human Molecular Genetics, 2014, 23, 6, 1516

    CrossRef

  3. 3
    Bettina Balint, Kailash P. Bhatia, Dystonia, Current Opinion in Neurology, 2014, 27, 4, 468

    CrossRef

  4. You have free access to this content4
    I. M. Skogseid, Dystonia – new advances in classification, genetics, pathophysiology and treatment, Acta Neurologica Scandinavica, 2014, 129,
  5. 5
    Lubov Blumkin, Ayelet Halevy, Dominique Ben-Ami-Raichman, Dvir Dahari, Ami Haviv, Cohen Sarit, Dorit Lev, Marjo S. van der Knaap, Tally Lerman-Sagie, Esther Leshinsky-Silver, Expansion of the spectrum of TUBB4A-related disorders: a new phenotype associated with a novel mutation in the TUBB4A gene, neurogenetics, 2014, 15, 2, 107

    CrossRef

  6. 6
    Rachel Saunders-Pullman, Tania Fuchs, Marta San Luciano, Deborah Raymond, Alison Brashear, Robert Ortega, Andres Deik, Laurie J. Ozelius, Susan B. Bressman, Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites, Movement Disorders, 2014, 29, 6
  7. 7
    E. M. Hamilton, E. Polder, A. Vanderver, S. Naidu, R. Schiffmann, K. Fisher, A. B. Ragu , L. Blumkin, C. G. M. van Berkel, Q. Waisfisz, C. Simons, R. J. Taft, T. E. M. Abbink, N. I. Wolf, M. S. van der Knaap, Hypomyelination with atrophy of the basal ganglia and cerebellum: further delineation of the phenotype and genotype-phenotype correlation, Brain, 2014, 137, 7, 1921

    CrossRef

  8. 8
    Romina Romaniello, Filippo Arrigoni, Maria Teresa Bassi, Renato Borgatti, Mutations in α- and β-tubulin encoding genes: Implications in brain malformations, Brain and Development, 2014,

    CrossRef

  9. 9
    Carlos Ferreira, Andrea Poretti, Julie Cohen, Ada Hamosh, Sakkubai Naidu, Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC), American Journal of Medical Genetics Part A, 2014, 164, 7
  10. 10
    Narges Moghimi, Bahman Jabbari, Anna M. Szekely, Primary dystonias and genetic disorders with dystonia as clinical feature of the disease, European Journal of Paediatric Neurology, 2014, 18, 1, 79

    CrossRef

  11. 11
    Jianfeng Xiao, Satya R. Vemula, Mark S. LeDoux, Recent Advances in the Genetics of Dystonia, Current Neurology and Neuroscience Reports, 2014, 14, 8

    CrossRef

  12. 12
    Katja Lohmann, Christine Klein, The many faces of TUBB4A mutations, neurogenetics, 2014, 15, 2, 81

    CrossRef

  13. 13
    Hieab H.H. Adams, Benjamin F.J. Verhaaren, Henri A. Vrooman, Andre G. Uitterlinden, Albert Hofman, Cornelia M. van Duijn, Aad van der Lugt, Wiro J. Niessen, Meike W. Vernooij, M. Arfan Ikram, TMEM106B Influences Volume of Left-Sided Temporal Lobe and Interhemispheric Structures in the General Population, Biological Psychiatry, 2014,

    CrossRef

  14. 14
    Tania Fuchs, Laurie J. Ozelius, Genetics in Dystonia: An Update, Current Neurology and Neuroscience Reports, 2013, 13, 12

    CrossRef

  15. 15
    Christine Klein, Alexander Münchau, Pediatric Neurology Part III, 2013,

    CrossRef