Toggle Main Menu Toggle Search

ePrints

Browsing publications by Dr Fiona Norwood

Newcastle AuthorsTitleYearFull text
Dr German Moris
Libby Wood
Roberto Fernandez-Torron
Dr Adela Cora
Dr Fiona Norwood
et al.
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophy2018
Dr Katherine Johnson
Dr Ana Topf
Dr Marta Bertoli
Lauren Phillips
Dr James Miller
et al.
Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population2018
Sila Hopton
Gavin Falkous
Dr Fiona Norwood
Dr Grainne Gorman
Professor Robert Taylor
et al.
Sideroblastic anemia with myopathy secondary to novel, pathogenic missense variants in the YARS2 gene2018
Libby Wood
Roberto Fernandez-Torron
Dr John Hudson
Dr Fiona Norwood
Dr Michela Guglieri
et al.
Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registry2016
Dr Anna Sarkozy
Dr Rita Barresi
Dr Marta Bertoli
Professor Katherine Bushby
Professor Hanns Lochmuller
et al.
Eight novel UK families further expand current knowledge on GMPPB-gene related dystroglycanopathies2015
Dr Teresinha Evangelista
Libby Wood
Dr Fiona Norwood
Professor Hanns Lochmuller
Pain and quality of life in the UK FSHD patient registry2015
Dr Amina Chaouch
Dr Fiona Norwood
Professor Rita Horvath
Professor Patrick Chinnery
Dr Tuomo Polvikoski
et al.
Two recurrent mutations are associated with GNE myopathy in the North of Britain2014
Dr Anna Sarkozy
Dr Debbie Hicks
Dr Steven Laval
Dr Rita Barresi
Dr Lizzie Harris
et al.
ANO5 Gene Analysis in a Large Cohort of Patients with Anoctaminopathy: Confirmation of Male Prevalence and High Occurrence of the Common Exon 5 Gene Mutation2013
Professor Volker Straub
Professor Hanns Lochmuller
Dr Anna Sarkozy
Dr Fiona Norwood
Professor Katherine Bushby
et al.
Clinical and genetic findings in a large cohort of patients with ryanodine receptor 1 gene associated myopathies (vol 33, pg 981, 2012)2012
Professor Volker Straub
Professor Hanns Lochmuller
Dr Anna Sarkozy
Dr Fiona Norwood
Professor Katherine Bushby
et al.
Clinical and Genetic Findings in a Large Cohort of Patients with Ryanodine Receptor 1 Gene-Associated Myopathies2012
12