Publications by Professor Michael Hanna - ePrints

Browsing publications by Professor Michael Hanna.

Newcastle Authors	Title	Year
Dr William Macken Dr Mahmoud Fassad Dr Fei Gao Krutik Patel Dr Ana Topf et al.	Neuromuscular disease genetics in under-represented populations: increasing data diversity	2023
Professor Chiara Marini Bettolo Professor Michael Hanna Emma Matthews	Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity	2022
Dr Chiara Pizzamiglio Dr Rhys Thomas Professor Grainne Gorman Professor Bobby McFarland Professor Michael Hanna et al.	COVID-19-Related Outcomes in Primary Mitochondrial Diseases: An International Study	2022
Dr Yi Ng Dr Nichola Lax Dr Alasdair Blain Dr Daniel Erskine Professor Mark Baker et al.	Forecasting stroke-like episodes and outcomes in mitochondrial disease	2022
Professor Michael Hanna Dr Ana Topf Professor Volker Straub	A form of muscular dystrophy associated with pathogenic variants in JAG2	2021
Dr Karen Suetterlin Professor Avan Sayer Professor Michael Hanna	Ageing Contributes to Phenotype Transition in a Mouse Model of Periodic Paralysis	2021
Dr Karen Suetterlin Professor Michael Hanna Emma Matthews	Andersen-Tawil Syndrome Presenting with Complete Heart Block	2021
Dr Karen Suetterlin Professor Michael Hanna	Annual renal ultrasound may prevent acute presentation with acetazolamide-associated urolithiasis	2021
Professor Rita Horvath Dr Wei Wei Dr Robert Pitceathly Professor Michael Hanna Professor John Sayer et al.	Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: Cohort study	2021
Dr Helen Griffin Dr Michele Giunta Benjamin Munro Dr Wei Wei Dr Veronika Boczonadi et al.	Metabolic shift underlies recovery in reversible infantile respiratory chain deficiency	2020
Dr Karen Suetterlin Professor Michael Hanna	Mexiletine (NaMuscla) for the treatment of myotonia in non-dystrophic myotonic disorders	2020
Professor Robert Taylor Professor Michael Hanna Dr Robert Pitceathly	Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNA^Gly(MT-TG) variant	2020
Dr Yi Ng Dr Mika Martikainen Professor Grainne Gorman Dr Alasdair Blain Dr Andrew Schaefer et al.	Pathogenic variants in MT-ATP6: A United Kingdom–based mitochondrial disease cohort study	2019
Dr James Miller Professor Michael Hanna	Cytosolic 5′-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis	2017
Professor Mike Trenell Professor Michael Hanna	Evaluating the benefits of community based aerobic training on the physical health and well-being of people with Charcot-Marie-Tooth disease type 1A	2016
Professor Mike Trenell Professor Michael Hanna	Evaluating the benefits of community based aerobic training on the physical health and well-being of people with neuromuscular disease	2016
Dr Karen Suetterlin Professor Michael Hanna	Muscle channelopathies	2016
Sebastian Figueroa Bonaparte Dr Rita Barresi Dr Tuomo Polvikoski Dr Timothy Williams Dr Ana Topf et al.	Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK	2016
Professor Mike Trenell Professor Michael Hanna	Normative aerobic exercise values in CMT	2016
Dr Charlotte Alston Dr Robert Pitceathly Professor Bobby McFarland Dr Andrew Schaefer Emeritus Professor Doug Turnbull et al.	The urinary proteome and metabonome differ from normal in adults with mitochondrial disease	2015
Dr Karen Suetterlin Professor Michael Hanna	Muscle channelopathies: recent advances in genetics, pathophysiology and therapy.	2014
Dr Tracey Willis Dr Kieren Hollingsworth Dr Michelle Eagle Dr Anna Mayhew Emerita Professor Katherine Bushby et al.	Quantitative Magnetic Resonance Imaging in Limb-Girdle Muscular Dystrophy 2I: A Multinational Cross-Sectional Study	2014
Dr Boglarka Bansagi Marina Bartsakoulia Professor Michael Hanna Professor Rita Horvath	Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 2	2014
Dr Anna Sarkozy Dr Debbie Hicks Dr Steven Laval Dr Rita Barresi Dr Lizzie Harris et al.	ANO5 Gene Analysis in a Large Cohort of Patients with Anoctaminopathy: Confirmation of Male Prevalence and High Occurrence of the Common Exon 5 Gene Mutation	2013
Dr Gerald Pfeffer Professor Rita Horvath Professor Laurence Bindoff Dr Patrick Yu Wai Man Professor Michael Hanna et al.	New treatments for mitochondrial disease - no time to drop our standards	2013
Dr Tracey Willis Dr Kieren Hollingsworth Dr Michelle Eagle Dr Anna Mayhew Emerita Professor Katherine Bushby et al.	Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study	2013
Dr Victoria Nesbitt Dr Robert Pitceathly Dr Simon Cockell Professor Michael Hanna Professor Patrick Chinnery et al.	The Medical Research Council Neuromuscular Centre for Translational Research Mitochondrial Disease Patient Cohort Study UK: From Conceptualisation to Utilisation	2013
Dr Nuria Muelas Gomez Professor Michael Hanna Dr Amina Chaouch Professor Volker Straub Emerita Professor Katherine Bushby et al.	Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations	2012
Dr Charlotte Alston Professor Rita Horvath Professor Michael Hanna Professor Patrick Chinnery Emeritus 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 Emeritus 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
Professor Michael Hanna Professor Robert Taylor Andy Duncan	Whole Exome Sequencing Reveals that Subunit Mutations are Prevalent in Complex I Deficient Leigh Syndrome	2012
Dr 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 Emerita 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