Toggle Main Menu Toggle Search

Open Access padlockePrints

Browsing publications by Professor Michael Hanna

Newcastle AuthorsTitleYearFull text
Dr Mahmoud Fassad
Dr Krutik Patel
Professor Michael Hanna
Professor Robert Taylor
Professor Bobby McFarland
Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort2025
Dr Chiara Pizzamiglio
Dr Renae Stefanetti
Professor Bobby McFarland
Dr Naomi Thomas
Professor Michael Hanna
et al.		Optimizing rare disorder trials: A phase 1a/1b randomized study of KL1333 in adults with mitochondrial disease2025
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 diversity2023
Professor Chiara Marini Bettolo
Professor Michael Hanna
Emma Matthews
Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity2022
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
Professor 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
123