Items where Author is "Kullmann, DM"

Rajakulendran, S and Graves, TD and Labrum, RW and Kotzadimitriou, D and Eunson, LH and Davis, MB and Davies, R and Wood, NW and Kullmann, DM and Hanna, MG and Schorge, S (2010) Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy. The Journal of Physiology, 588 (11). pp. 1905-1913. DOI https://doi.org/10.1113/jphysiol.2009.186437

Labrum, RW and Rajakulendran, S and Graves, TD and Eunson, LH and Bevan, R and Sweeney, MG and Hammans, SR and Tubridy, N and Britton, T and Carr, LJ and Ostergaard, JR and Kennedy, CR and Al-Memar, A and Kullmann, DM and Schorge, S and Temple, K and Davis, MB and Hanna, MG (2009) Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing. Journal of Medical Genetics, 46 (11). pp. 786-791. DOI https://doi.org/10.1136/jmg.2009.067967

Graves, TD and Imbrici, P and Kors, EE and Terwindt, GM and Eunson, LH and Frants, RR and Haan, J and Ferrari, MD and Goadsby, PJ and Hanna, MG and van den Maagdenberg, AMJM and Kullmann, DM (2008) Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2. Neurobiology of Disease, 32 (1). pp. 10-15. DOI https://doi.org/10.1016/j.nbd.2008.06.002