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Browsing publications by Professor Michael Hanna.

Newcastle AuthorsTitleYearFull text
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 Study2022
Dr Yi Ng
Dr Nichola Lax
Dr Alasdair Blain
Dr Daniel Erskine
Dr Mark Baker
et al.
Forecasting stroke-like episodes and outcomes in mitochondrial disease2022
Professor Michael Hanna
Dr Ana Topf
Professor Volker Straub
A form of muscular dystrophy associated with pathogenic variants in JAG22021
Dr Karen Suetterlin
Professor Avan Sayer
Professor Michael Hanna
Ageing Contributes to Phenotype Transition in a Mouse Model of Periodic Paralysis2021
Dr Karen Suetterlin
Professor Michael Hanna
Emma Matthews
Andersen-Tawil Syndrome Presenting with Complete Heart Block2021
Dr Karen Suetterlin
Professor Michael Hanna
Annual renal ultrasound may prevent acute presentation with acetazolamide-associated urolithiasis2021
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 study2021
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 deficiency2020
Dr Karen Suetterlin
Professor Michael Hanna
Mexiletine (NaMuscla) for the treatment of myotonia in non-dystrophic myotonic disorders2020
Professor Robert Taylor
Professor Michael Hanna
Dr Robert Pitceathly
Multisystem mitochondrial disease caused by a rare m.10038G>A mitochondrial tRNAGly (MT-TG) variant2020
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 study2019
Dr James Miller
Professor Michael Hanna
Cytosolic 5′-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositis2017
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 1A2016
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 disease2016
Dr Karen Suetterlin
Professor Michael Hanna
Muscle channelopathies2016
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 UK2016
Professor Mike Trenell
Professor Michael Hanna
Normative aerobic exercise values in CMT2016
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 disease2015
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 Study2014
Dr Boglarka Bansagi
Marina Bartsakoulia
Professor Michael Hanna
Professor Rita Horvath
Truncating and Missense Mutations in IGHMBP2 Cause Charcot-Marie Tooth Disease Type 22014
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 Mutation2013
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 standards2013
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 Study2013
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 Utilisation2013
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 mutations2012
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 disease2012
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 utilisation2012
Professor Michael Hanna
Professor Robert Taylor
Andy Duncan
Whole Exome Sequencing Reveals that Subunit Mutations are Prevalent in Complex I Deficient Leigh Syndrome2012
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 deletions2011
Dr Tracey Willis
Dr Kieren Hollingsworth
Dr Michelle Eagle
Dr Anna Mayhew
Emerita Professor Katherine Bushby
et al.
Quantitative MRI in LGMD2I; a longitudinal study2011
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 channel2001
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 function2000
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 Encephalomyopathy1999
Dr Vankateswara Ramesh
Professor Michael Hanna
New mutations in the voltage-gated calcium channel gene CACNA1A in british families with episodic ataxia type 21999