Toggle Main Menu Toggle Search

Open Access padlockePrints

Browsing publications by Dr Oksana Pogoryelova

Newcastle AuthorsTitleYearFull text
Matt Birkbeck
Dr Mat Elameer
Dr Linda Heskamp
Jane Newman
Dr Renae Stefanetti
et al.		Measurement of Twitch Dynamics in Response to Exercise Induced Changes in Mitochondrial Disease Using Motor Unit Magnetic Resonance Imaging (MUMRI): A Proof-of-Concept Study2025
Dr Oksana Pogoryelova
GNE Myopathy: Genotype – Phenotype Correlation and Disease Progression in an Indian Cohort2024
Dr Andreas Roos
Dr Oksana Pogoryelova
Dr Sally Spendiff
Professor Hanns Lochmuller
Ion Mobility QTOF-MS Untargeted Lipidomics of Human Serum Reveals a Metabolic Fingerprint for GNE Myopathy2024
Professor Hanns Lochmuller
Dr Oksana Pogoryelova
A phase 3 randomized study evaluating sialic acid extended-release for GNE myopathy2021
Professor Hanns Lochmuller
Professor Rita Horvath
Dr Oksana Pogoryelova
Results from a 3-year Non-interventional, Observational Disease Monitoring Program in Adults with GNE Myopathy2021
Dr Oksana Pogoryelova
Professor Hanns Lochmuller
Economic Costs of Myasthenia Gravis: A Systematic Review2020
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
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
Professor Michela Guglieri
Professor 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
12