Edinburgh Research Explorer
  1. 2005
  2. Early management of adults with an uncomplicated first generalised seizure

    Dunn, M. J. G., Breen, D. P., Davenport, R. J. & Gray, A. J., Apr 2005, In : Emergency Medicine Journal. 22, 4, p. 237-42 6 p.

    Research output: Contribution to journalReview article

  3. Epidemiology, clinical characteristics, and management of adults referred to a teaching hospital first seizure clinic

    Breen, D. P., Dunn, M. J. G., Davenport, R. J. & Gray, A. J., Nov 2005, In : Postgraduate Medical Journal. 81, 961, p. 715-8 4 p.

    Research output: Contribution to journalArticle

  4. 2006
  5. Teratogenicity of antiepileptic drugs

    Breen, D. P. & Davenport, R. J., 23 Sep 2006, In : BMJ (Clinical research ed.). 333, 7569, p. 615-6 2 p.

    Research output: Contribution to journalArticle

  6. 2007
  7. FGF stimulation of the Erk1/2 signalling cascade triggers transition of pluripotent embryonic stem cells from self-renewal to lineage commitment

    Kunath, T., Saba-El-Leil, M. K., Almousailleakh, M., Wray, J., Meloche, S. & Smith, A., 1 Aug 2007, In : Development. 134, 16, p. 2895-2902 8 p.

    Research output: Contribution to journalArticle

  8. 2008
  9. A Small Trinucleotide Expansion in the TBP Gene Gives Rise to a Sporadic Case of SCA17 with Abnormal Putaminal Findings on MRI

    Watanabe, M., Monai, N., Jackson, M., Yamamoto-Watanabe, Y., Ikeda, Y., Suzuki, C., Tomiyama, M., Kawarabayashi, T., Kimura, T., Seino, Y., Wakasaya, Y., Miki, Y., Matsubara, E. & Shoji, M., 2008, In : Internal Medicine. 47, 24, p. 2179-2182 4 p.

    Research output: Contribution to journalArticle

  10. 2009
  11. Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

    Ali, M., McKibbin, M., Booth, A., Parry, D. A., Jain, P., Riazuddin, S. A., Hejtmancik, J. F., Khan, S. N., Firasat, S., Shires, M., Gilmour, D. F., Towns, K., Murphy, A. L., Azmanov, D., Tournev, I., Cherninkova, S., Jafri, H., Raashid, Y., Toomes, C., Craig, J. & 4 others, Mackey, D. A., Kalaydjieva, L., Riazuddin, S. & Inglehearn, C. F., 15 May 2009, In : American Journal of Human Genetics. 84, 5, p. 664-671 8 p.

    Research output: Contribution to journalArticle

  12. Mutations in the Beta Propeller WDR72 Cause Autosomal-Recessive Hypomaturation Amelogenesis Imperfecta

    El-Sayed, W., Parry, D. A., Shore, R. C., Ahmed, M., Jafri, H., Rashid, Y., Al-Bahlani, S., Al Harasi, S., Kirkham, J., Inglehearn, C. F. & Mighell, A. J., 13 Nov 2009, In : American Journal of Human Genetics. 85, 5, p. 699-705 7 p.

    Research output: Contribution to journalArticle

  13. 2010
  14. β-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi

    Clarkson, Y., Gillespie, T., Perkins, E. M., Lyndon, A. R. & Jackson, M., Sep 2010, In : Human Molecular Genetics. 19, 18, p. 3634-3641 8 p.

    Research output: Contribution to journalArticle

  15. A Japanese ALS6 family with mutation R521C in the FUS/TLS gene: A clinical, pathological and genetic report

    Yamamoto-Watanabe, Y., Watanabe, M., Okamoto, K., Fujita, Y., Jackson, M., Ikeda, M., Nakazato, Y., Ikeda, Y., Matsubara, E., Kawarabayashi, T. & Shoji, M., 15 Sep 2010, In : Journal of the Neurological Sciences. 296, 1-2, p. 59-63 5 p.

    Research output: Contribution to journalArticle

  16. 2011
  17. β-III spectrin is critical for development of purkinje cell dendritic tree and spine morphogenesis

    Gao, Y., Perkins, E. M., Clarkson, Y. L., Tobia, S., Lyndon, A. R., Jackson, M. & Rothstein, J. D., 2011, In : Journal of Neuroscience. 31, 46, p. 16581-90 10 p.

    Research output: Contribution to journalArticle

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