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Browsing publications by Dr Stephen Lynn.

Newcastle AuthorsTitleYearFull text
Dr Stephen Lynn
Duchenne regulatory science consortium meeting on disease progression modeling for duchenne muscular dystrophy2017
Dr Teresinha Evangelista
Victoria Hedley
Dr Jose Atalaia
Dr Stephen Lynn
Emerita Professor Katherine Bushby
et al.
The context for the thematic grouping of rare diseases to facilitate the establishment of European Reference Networks2016
Dr Stephen Lynn
Professor Annemieke Aartsma-Rus
Emerita Professor Katherine Bushby
Dr Anna Mayhew
Professor Volker Straub
et al.
Measuring clinical effectiveness of medicinal products for the treatment of Duchenne muscular dystrophy2015
Dr Stephen Lynn
Dr Monica Ensini
Dr Mojgan Reza
Professor Hanns Lochmuller
The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases2015
Emerita Professor Katherine Bushby
Dr Stephen Lynn
Professor Volker Straub
Collaborating to bring new therapies to the patient - The TREAT-NMD model2009
Emerita Professor Katherine Bushby
Professor Hanns Lochmuller
Dr Stephen Lynn
Professor Volker Straub
Interventions for muscular dystrophy:molecular medicines entering the clinic2009
Dr Lynsey Cree
Dr Sheila Patel
Dr Angela Pyle
Dr Stephen Lynn
Emeritus Professor Doug Turnbull
et al.
Age-related decline in mitochondrial DNA copy number in isolated human pancreatic islets2008
Professor Bobby McFarland
Dr Andrew Schaefer
Dr Julie Murphy
Dr Stephen Lynn
Christine Hayes
et al.
Familial Myopathy: New Insights into the T14709C Mitochondrial tRNA Mutation2004
Dr Andrew Schaefer
Professor Bobby McFarland
Dr Julie Murphy
Dr Stephen Lynn
Christine Hayes
et al.
Familial mitochondrial myopathy: New insights into the T14709C mitochondrial tRNA mutation2003
Dr Stephen Lynn
Dr Gillian Borthwick
Richard Charnley
Professor Mark Walker
Emeritus Professor Doug Turnbull
et al.
Heteroplasmic ratio of the A3243G mitochondrial DNA mutation in single pancreatic beta cells2003
Dr Stephen Lynn
Geoffrey Taylor
Dr Theresa Wardell
Professor Patrick Chinnery
Emeritus Professor Doug Turnbull
et al.
Defining the importance of mitochondrial gene defects in maternally inherited diabetes by sequencing the entire mitochondrial genome2002
Dr Stephen Lynn
Emeritus Professor Doug Turnbull
Professor Mark Walker
Intermediate expansions of a X25/frataxin gene GAA repeat and Type II diabetes: Assessment using parent-offspring trios [1]2000
Dr Stephen Lynn
Anne Hattersley
Emeritus Professor Doug Turnbull
Professor Mark Walker
Intermediate GAA repeat expansions of the X25/frataxin gene in type 2 diabetes1999