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Browsing publications by
Phillip Cammish.
Newcastle Authors
Title
Year
Full text
Phillip Cammish
Dr Teresinha Evangelista
Professor Volker Straub
Professor Chiara Marini Bettolo
Facioscapulohumeral muscular dystrophy 1 patients participating in the UK FSHD registry can be subdivided into 4 patterns of self-reported symptoms
2020
Giulia Ricci
Phillip Cammish
Professor Hanns Lochmuller
Dr Teresinha Evangelista
Phenotype may predict the clinical course of facioscapolohumeral muscular dystrophy
2019
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 Research
2019
Ben Porter
Phillip Cammish
Emma Heslop
Professor Chiara Marini Bettolo
The UK Myotonic Dystrophy Patient Registry: A Key Tool in the Facilitation of Clinical Research
2019
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 portion
2018
Dr Oksana Pogoryelova
Phillip Cammish
Professor Hanns Lochmuller
GNE myopathy worldwide epidemiology based on the patient self-reported registry
2015