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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Michael G. Hanna

National Hospital for Neurology and Neurosurgery

Queen Square




Name/email consistency: high



  • National Hospital for Neurology and Neurosurgery, Queen Square, London, UK. 2006
  • Department of Molecular Neuroscience and Centre for Neuromuscular Disease, National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK. 2005
  • Neurogenetics Section, University Department of Clinical Neurology, Institute of Neurology, London, United Kingdom. 1998 - 2001
  • Department of Clinical Neurology, Institute of Neurology, London, UK. 1998 - 1999


  1. Genetic neurological channelopathies. Hanna, M.G. Nature Clinical Practice. Neurology (2006) [Pubmed]
  2. Neurological channelopathies. Graves, T.D., Hanna, M.G. Postgrad. Med. J (2005) [Pubmed]
  3. Inherited muscle and brain channelopathies. Davies, N.P., Hanna, M.G. Expert. Rev. Neurother (2001) [Pubmed]
  4. Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases. Hanna, M.G., Nelson, I.P. Cell. Mol. Life Sci. (1999) [Pubmed]
  5. Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA. Hanna, M.G., Nelson, I.P., Rahman, S., Lane, R.J., Land, J., Heales, S., Cooper, M.J., Schapira, A.H., Morgan-Hughes, J.A., Wood, N.W. Am. J. Hum. Genet. (1998) [Pubmed]
  6. Salbutamol treatment in a patient with hyperkalaemic periodic paralysis due to a mutation in the skeletal muscle sodium channel gene (SCN4A). Hanna, M.G., Stewart, J., Schapira, A.H., Wood, N.W., Morgan-Hughes, J.A., Murray, N.M. J. Neurol. Neurosurg. Psychiatr. (1998) [Pubmed]
  7. MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity. Hanna, M.G., Nelson, I.P., Morgan-Hughes, J.A., Wood, N.W. J. Neurol. Neurosurg. Psychiatr. (1998) [Pubmed]
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