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Browsing publications by Dr Boglarka Bansagi

Newcastle AuthorsTitleYearFull text
Dr Veronika Boczonadi
Dr Monika Olahova
Dr Boglarka Bansagi
Dr Andreas Roos
Dr Vankateswara Ramesh
et al.		Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease2018
Dr Veronika Boczonadi
Dr Helen Griffin
Dr Andreas Roos
Marina Bartsakoulia
Dr Boglarka Bansagi
et al.		Mutations in glycyl-tRNA synthetase impair mitochondrial metabolism in neurons2018
Professor Rita Horvath
Dr Boglarka Bansagi
Novel SBF2 mutations and clinical spectrum of Charcot-Marie-Tooth neuropathy type 4B22018
Dr Boglarka Bansagi
Dr John O'Sullivan
Dr Juliane Mueller
Dr Jennifer Duff
Dr Grainne Gorman
et al.		Multifocal motor neuropathy caused by phosphatase and tensin homologue (PTEN) mutation2016
Dr Veronika Boczonadi
Marina Bartsakoulia
Dr Boglarka Bansagi
Dr Francesco Bruni
Dr Juliane Mueller
et al.		Mutations in glycyl-tRNA-synthetase impair mitochondrial function in neurons2016
Dr Veronika Boczonadi
Marina Bartsakoulia
Dr Boglarka Bansagi
Dr Francesco Bruni
Dr Juliane Mueller
et al.		Mutations in glycyl-tRNA-synthetase impair mitochondrial function in neurons2016
Professor Roger Whittaker
Dr Boglarka Bansagi
Professor Hanns Lochmuller
Professor Rita Horvath
Clinical and Neurophysiological findings in synaptotagmin 2 mutations: a novel and potentially treatable neuromuscular disease2015
Professor Roger Whittaker
Dr Boglarka Bansagi
Professor Rita Horvath
Professor Hanns Lochmuller
Electrophysiologic features of SYT2 mutations causing a treatable neuromuscular syndrome2015
Dr Boglarka Bansagi
Professor Hanns Lochmuller
Professor Patrick Chinnery
Professor Rita Horvath
Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland2015
Dr Teresinha Evangelista
Dr Boglarka Bansagi
Dr Angela Pyle
Dr Helen Griffin
Dr Konstantinos Douroudis
et al.		Phenotypic variability of TRPV4 related neuropathies2015
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