Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis
Matthews, E, Labrum, R, Sweeney, M G, Sud, R, Haworth, A, Chinnery, P F, Meola, G, Schorge, S, Kullmann, D M, Davis, M B, Hanna, M G
Published in Neurology (05.05.2009)
Published in Neurology (05.05.2009)
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A Comparison of Vancomycin and Metronidazole for the Treatment of Clostridium difficile–Associated Diarrhea, Stratified by Disease Severity
Zar, Fred A., Bakkanagari, Srinivasa R., Moorthi, K. M. L. S. T., Davis, Melinda B.
Published in Clinical infectious diseases (01.08.2007)
Published in Clinical infectious diseases (01.08.2007)
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Journal Article
Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients
Trender-Gerhard, I, Sweeney, M G, Schwingenschuh, P, Mir, P, Edwards, M J, Gerhard, A, Polke, J M, Hanna, M G, Davis, M B, Wood, N W, Bhatia, K P
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2009)
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Journal Article
Acetazolamide efficacy in hypokalemic periodic paralysis and the predictive role of genotype
Matthews, E, Portaro, S, Ke, Q, Sud, R, Haworth, A, Davis, M B, Griggs, R C, Hanna, M G
Published in Neurology (29.11.2011)
Published in Neurology (29.11.2011)
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Journal Article
Range Shifts and Adaptive Responses to Quaternary Climate Change
Davis, Margaret B., Shaw, Ruth G.
Published in Science (American Association for the Advancement of Science) (27.04.2001)
Published in Science (American Association for the Advancement of Science) (27.04.2001)
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Journal Article
Chloride channel myotonia: exon 8 hot-spot for dominant-negative interactions
Fialho, D., Schorge, S., Pucovska, U., Davies, N. P., Labrum, R., Haworth, A., Stanley, E., Sud, R., Wakeling, W., Davis, M. B., Kullmann, D. M., Hanna, M. G.
Published in Brain (London, England : 1878) (01.12.2007)
Published in Brain (London, England : 1878) (01.12.2007)
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Journal Article
Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort
Davidson, G. L., Murphy, S. M., Polke, J. M., Laura, M., Salih, M. A. M., Muntoni, F., Blake, J., Brandner, S., Davies, N., Horvath, R., Price, S., Donaghy, M., Roberts, M., Foulds, N., Ramdharry, G., Soler, D., Lunn, M. P., Manji, H., Davis, M. B., Houlden, H., Reilly, M. M.
Published in Journal of neurology (01.08.2012)
Published in Journal of neurology (01.08.2012)
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Journal Article
TRPV1 and TRPA1 function and modulation are target tissue dependent
Malin, Sacha, Molliver, Derek, Christianson, Julie A, Schwartz, Erica S, Cornuet, Pam, Albers, Kathryn M, Davis, Brian M
Published in The Journal of neuroscience (20.07.2011)
Published in The Journal of neuroscience (20.07.2011)
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Journal Article
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations
Polke, J M, Laurá, M, Pareyson, D, Taroni, F, Milani, M, Bergamin, G, Gibbons, V S, Houlden, H, Chamley, S C, Blake, J, Devile, C, Sandford, R, Sweeney, M G, Davis, M B, Reilly, M M
Published in Neurology (12.07.2011)
Published in Neurology (12.07.2011)
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Journal Article
A new explanation for recessive myotonia congenita: exon deletions and duplications in CLCN1
Raja Rayan, D L, Haworth, A, Sud, R, Matthews, E, Fialho, D, Burge, J, Portaro, S, Schorge, S, Tuin, K, Lunt, P, McEntagart, M, Toscano, A, Davis, M B, Hanna, M G
Published in Neurology (12.06.2012)
Published in Neurology (12.06.2012)
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Journal Article
What causes paramyotonia in the United Kingdom? Common and new SCN4A mutations revealed
Matthews, E, Tan, S V, Fialho, D, Sweeney, M G, Sud, R, Haworth, A, Stanley, E, Cea, G, Davis, M B, Hanna, M G
Published in Neurology (01.01.2008)
Published in Neurology (01.01.2008)
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Journal Article
Basic and clinical aspects of visceral sensation: transmission in the CNS
Bielefeldt, K., Christianson, J. A., Davis, B. M.
Published in Neurogastroenterology and motility (01.08.2005)
Published in Neurogastroenterology and motility (01.08.2005)
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Journal Article
Large scale calcium channel gene rearrangements in episodic ataxia and hemiplegic migraine: implications for diagnostic testing
Labrum, R W, Rajakulendran, S, Graves, T D, Eunson, L H, Bevan, R, Sweeney, M G, Hammans, S R, Tubridy, N, Britton, T, Carr, L J, Ostergaard, J R, Kennedy, C R, Al-Memar, A, Kullmann, D M, Schorge, S, Temple, K, Davis, M B, Hanna, M G
Published in Journal of medical genetics (01.11.2009)
Published in Journal of medical genetics (01.11.2009)
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Journal Article
Deletion of P2X3 receptors blunts gastro‐oesophageal sensation in mice
Mcilwrath, S. L., Davis, B. M., Bielefeldt, K.
Published in Neurogastroenterology and motility (01.08.2009)
Published in Neurogastroenterology and motility (01.08.2009)
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