Michael G. Hanna
National Hospital for Neurology and Neurosurgery
Queen Square
London
UK
Name/email consistency: high
- Genetic neurological channelopathies. Hanna, M.G. Nature Clinical Practice. Neurology (2006)
- Neurological channelopathies. Graves, T.D., Hanna, M.G. Postgrad. Med. J (2005)
- Inherited muscle and brain channelopathies. Davies, N.P., Hanna, M.G. Expert. Rev. Neurother (2001)
- Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases. Hanna, M.G., Nelson, I.P. Cell. Mol. Life Sci. (1999)
- 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)
- 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)
- 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)