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Browsing publications by Dr Oksana Pogoryelova

Newcastle AuthorsTitleYearFull text
Dr Oksana Pogoryelova
Dr Ian Wilson
Professor Hanns Lochmuller
GNE genotype explains 20% of phenotypic variability in GNE myopathy2019
Dr Oksana Pogoryelova
Professor Hanns Lochmuller
Dr Andreas Roos
Dr Verena Willenbockel
237th ENMC International Workshop: GNE myopathy – current and future research Hoofddorp, The Netherlands, 14–16 September 20182019
Dr Hadil Alrohaif
Dr Oksana Pogoryelova
Professor Hanns Lochmuller
Gne myopathy in the bedouin population of Kuwait: Genetics, prevalence, and clinical description2018
Dr Oksana Pogoryelova
Jose Gonzalez Coraspe
Dr Nikoletta Nikolenko
Professor Hanns Lochmuller
Dr Andreas Roos
et al.
GNE myopathy: From clinics and genetics to pathology and research strategies2018
Dr Oksana Pogoryelova
Phillip Cammish
Professor Hanns Lochmuller
Phenotypic stratification and genotype–phenotype correlation in a heterogeneous, international cohort of GNE myopathy patients: First report from the GNE myopathy Disease Monitoring Program, registry portion2018
Dr Oksana Pogoryelova
Dr Michela Guglieri
Dr Chiara Marini Bettolo
Professor Volker Straub
Dr Teresinha Evangelista
et al.
Reduced serum myostatin concentrations associated with genetic muscle disease progression2017
Dr Oksana Pogoryelova
Professor Hanns Lochmuller
Beevor's sign: a potential clinical marker for GNE myopathy2016
Dr Oksana Pogoryelova
Professor Hanns Lochmuller
Upper and lower extremity muscle strength decline over 1 year in a prospective, observational GNE-myopathy natural history study2016
Dr Oksana Pogoryelova
Professor Hanns Lochmuller
GNE myopathy in Roma patients homozygous for the p.I618T founder mutation2015
Dr Oksana Pogoryelova
Phillip Cammish
Professor Hanns Lochmuller
GNE myopathy worldwide epidemiology based on the patient self-reported registry2015
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