Browsing publications by Professor Michael Hanna

Newcastle Authors	Title	Year
Dr Nuria Muelas Gomez Professor Michael Hanna Dr Amina Chaouch Professor Volker Straub Professor Katherine Bushby et al.	Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations	2012
Charlotte Alston Dr Rita Horvath Professor Michael Hanna Professor Patrick Chinnery Professor Doug Turnbull et al.	Expanding the phenotypic and genotypic spectrum of adult RRM2B-related mitochondrial disease	2012
Dr Victoria Nesbitt Dr Robert Pitceathly Dr Simon Cockell Professor Michael Hanna Professor Doug Turnbull et al.	The medical research council neuromuscular centre for translational research mitochondrial disease patient cohort study UK: from conceptualisation to utilisation	2012
Charlotte Alston Dr Robert Pitceathly Professor Michael Hanna Dr Andrew Schaefer Professor Patrick Chinnery et al.	Dominant and recessive RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions	2011
Dr Tracey Willis Dr Kieren Hollingsworth Dr Michelle Eagle Dr Anna Mayhew Professor Katherine Bushby et al.	Quantitative MRI in LGMD2I; a longitudinal study	2011
Professor Patrick Chinnery Dr Timothy Walls Professor Michael Hanna Emeritus Professor David Bates Dr Peter Fawcett et al.	Normokalemic periodic paralysis revisited: Does it exist?	2002
Dr Vankateswara Ramesh Professor Michael Hanna	Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel	2001
Dr Vankateswara Ramesh Professor Michael Hanna	Premature termination in the CACNA1A gene observed in episodic ataxia type 2 (EA2) results in a loss of alpha1A calcium channel function	2000
Professor Robert Taylor Dr Margaret Johnson Professor Patrick Chinnery Professor Zofia Chrzanowska-Lightowlers Professor Michael Hanna et al.	An mtDNA Mutation in the Initiation Codon of the Cytochrome C Oxidase Subunit II Gene Results in Lower Levels of the Protein and a Mitochondrial Encephalomyopathy	1999
Dr Vankateswara Ramesh Professor Michael Hanna	New mutations in the voltage-gated calcium channel gene CACNA1A in british families with episodic ataxia type 2	1999