Publications by Emma Heslop - ePrints

Browsing publications by Emma Heslop.

Newcastle Authors	Title	Year
Dr Marianela Schiava Robert Muni Lofra Dr John Bourke Meredith James Professor Jordi Diaz Manera et al.	Disease-associated comorbidities, medication records and anthropometric measures in adults with Duchenne muscular dystrophy	2024
Dr Marianela Schiava Dr John Bourke Meredith James Dr Maha Elseed Dr Monika Malinova et al.	Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids	2024
Victoria Hedley Becca Leary Dr Anando Sen Anna Irvin Emma Heslop et al.	Performing clinical drug trials in children with a rare disease	2024
Emma Heslop Catherine Turner Anna Irvin Professor Volker Straub Professor Michela Guglieri et al.	Gene therapy in Duchenne muscular dystrophy: Identifying and preparing for the challenges ahead	2021
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
Emma Heslop Professor Volker Straub Emerita Professor Katherine Bushby	The TREAT-NMD advisory committee for therapeutics (TACT): an innovative de-risking model to foster orphan drug development	2015
Emma Heslop Professor Volker Straub Dr Louise Johnston Emerita Professor Katherine Bushby	The TREAT-NMD Advisory Committee for Therapeutics (TACT): An innovative de-risking model to foster orphan drug development	2015
Rachel Thompson Dr Louise Johnston Dr Monica Ensini Emma Heslop Emerita Professor Katherine Bushby et al.	RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research	2014
Dr Pauline McCormack Emeritus Professor Simon Woods Emma Heslop Professor Volker Straub Emerita Professor Katherine Bushby et al.	Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational	2013
Emma Heslop Dr Pauline McCormack Professor Christoph Rehmann-Sutter Emeritus Professor Simon Woods	The risks of therapeutic misconception and individual patient (n = 1) “trials” in rare diseases such as Duchenne dystrophy	2011
Emerita Professor Katherine Bushby Emma Heslop Dr Pauline McCormack Emeritus Professor Simon Woods	The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: Report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009	2010