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Browsing publications by Ben Porter.

Newcastle AuthorsTitleYearFull text
Ben Porter
1st FSHD European Trial Network workshop: working towards trial readiness across Europe2021
Ben Porter
Robert Muni Lofra
Professor Chiara Marini Bettolo
Characterising FSHD and supporting national and international research projects: eight years of the UK FSHD Patient Registry2021
Ben Porter
Professor Chiara Marini Bettolo
Characterising myotonic dystrophy (DM) and supporting national and international research projects: nine years of the UK DM patient registry2021
Joanne Bullivant
Ben Porter
Dr Lindsay Murphy
Professor Chiara Marini Bettolo
Myotubular and centronuclear myopathy patient registry: Accelerating the pace of research and treatment2021
Ben Porter
Joanne Bullivant
Lucy Imber
Dr Lindsay Murphy
Relevance of maximal performance measurement during real-life ambulation in neuromuscular diseases: patients' and caregiver perspectives2021
Ben Porter
Robert Muni Lofra
Professor Chiara Marini Bettolo
The UK FSHD Patient Registry: Linking Patients to National and Internationals Research Projects2021
Ben Porter
The UK Myotonic Dystrophy Patient Registry: Linking Patients to National and International Research Projects2021
Ben Porter
Phillip Cammish
Joseph Orrell
Emma Heslop
Professor Chiara Marini Bettolo
et al.
The UK FSHD Patient Registry: A Key Tool in the Facilitation of Clinical Research2019
Ben Porter
Phillip Cammish
Emma Heslop
Professor Chiara Marini Bettolo
The UK Myotonic Dystrophy Patient Registry: A Key Tool in the Facilitation of Clinical Research2019