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Browsing publications by Dr Michela Guglieri

Newcastle AuthorsTitleYearFull text
Emerita Professor Katherine Bushby
Dr Michela Guglieri
Professor Volker Straub
Fractures and Linear Growth in a Nationwide Cohort of Boys with Duchenne Muscular Dystrophy with and Without Glucocorticoid Treatment: Results from the UK NorthStar Database2019
Dr Claire Wood
Dr Timothy Cheetham
Dr Kieren Hollingsworth
Dr Michela Guglieri
Dr Anna Mayhew
et al.
Observational study of clinical outcomes for testosterone treatment of pubertal delay in Duchenne muscular dystrophy2019
Dr Lizzie Harris
Dr Chiara Marini Bettolo
Dr Ana Topf
Dr Rita Barresi
Dr Tuomo Polvikoski
et al.
MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypes2018
Rebecca Crow
Professor Elaine McColl
Dr Jennifer Wilkinson
Dr Michelle Eagle
Professor Hanns Lochmuller
et al.
A checklist for clinical trials in rare disease: obstacles and anticipatory actions—lessons learned from the FOR-DMD trial2018
Dr Michela Guglieri
A multinational study on motor function in early-onset FSHD2018
Dr Michela Guglieri
Phase IIa trial in Duchenne muscular dystrophy shows vamorolone is a first-in-class dissociative steroidal anti-inflammatory drug2018
Dr John Bourke
Gillian Watson
Dr Michela Guglieri
Chris Speed
Professor Elaine McColl
et al.
Randomised placebo-controlled trial of combination ACE inhibitor and beta-blocker therapy to prevent cardiomyopathy in children with Duchenne muscular dystrophy? (DMD Heart Protection Study): a protocol study2018
Dr Michela Guglieri
Dr Alexander Murphy
Professor Katherine Bushby
Dr John Bourke
Cardiac involvement in female carriers of duchenne or becker muscular dystrophy2017
Dr Michela Guglieri
Professor Katherine Bushby
Professor Elaine McColl
Dr Jennifer Wilkinson
Dr Michelle Eagle
et al.
Developing standardized corticosteroid treatment for Duchenne muscular dystrophy2017
Dr Cecilia Jimenez Moreno
Cecilia Jimenez Moreno
Dr Nikoletta Nikolenko
Dr Jose Atalaia
Dr Michela Guglieri
et al.
Functional impairment in patients with myotonic dystrophy type 1 can be assessed by an ataxia rating scale (SARA)2017
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