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Browsing publications by Dr Andreas Roos

Newcastle AuthorsTitleYearFull text
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 Veronika Boczonadi
Dr Monika Olahova
Dr Boglárka Bánsági
Dr Andreas Roos
Dr Vankateswara Ramesh
et al.
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease (Genetics in Medicine, (2018), 20, 10, (1224-1235), 10.1038/gim.2017.251)2019
Daniel Cox
Silvia Cipriani
Dr Sally Spendiff
Emily O'Connor
Professor Rita Horvath
et al.
SIL1 deficiency causes degenerative changes of peripheral nerves and neuromuscular junctions in fish, mice and human2019
Emily O'Connor
Dr Ana Topf
Dr Sally Spendiff
Daniel Cox
Dr Andreas Roos
et al.
Clinical and research strategies for limb-girdle congenital myasthenic syndromes2018
Dr Sally Spendiff
Emeritus Professor Clarke Slater
Dr Andreas Roos
Professor Hanns Lochmuller
GFPT1 deficiency in muscle leads to myasthenia and myopathy in mice2018
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 Andreas Roos
Rachel Thompson
Professor Rita Horvath
Professor Hanns Lochmuller
Intersection of Proteomics and Genomics to "Solve the Unsolved" in Rare Disorders such as Neurodegenerative and Neuromuscular Diseases2018
Dr Andreas Roos
JAK inhibitor improves type i interferon induced damage: Proof of concept in dermatomyositis2018
Stephanie Carr
Professor Hanns Lochmuller
Dr Andreas Roos
Mass spectrometry-based protein analysis to unravel the tissue pathophysiology in Duchenne muscular dystrophy2018
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
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