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Welcome Dr Rebecca Mawby - PURA Syndrome Foundation awards first Fellowship Grant

Clinical research fellow position at University of Southampton to establish and administer the Global Patient Registry, undertake research into the Natural History of PURA syndrome and publish future papers.

 

June 2018 - The PURA Syndrome Foundation previously announced that it had awarded a research grant to the University of Southampton, in the United Kingdom.  The £20,000 (approx. $26,700) grant directly fulfils a portion of the Foundation’s mission to further research into this rare genetic condition.  The funds were raised by families and friends affected by PURA syndrome. 

 

This research grant will help fund an 18-month position at the University of Southampton. This role is jointly funded by the Foundation and by an anonymous donor to the University of Southampton, UK. The successful applicant will help develop and administer a secure global online patient registry. Information from this registry will form the basis of future research papers and help us to better understand what happens with PURA syndrome across the life span of patients (longitudinal study), creating a Natural History of the syndrome.

 

Both the study and Fellow will be overseen by the grant applicant, Prof Dr Diana Baralle. Dr Baralle holds a prestigious NIHR Research Professorship. As a Professor of Genomic Medicine and Clinical Geneticist, Prof Dr Diana Baralle’s research spans clinical phenotyping, diagnostics, and molecular mechanisms. Her clinic provides a rich resource for genetics and genomics research finding new causes for rare disorders. Dr Baralle’s laboratory takes this further by studying the molecular mechanisms in pre mRNA splicing which will helps them improve diagnostic testing, understand how genes work and therefore how they can modify them for gene therapy.

 

“This grant is a great accomplishment for the foundation and will provide an exciting next step in PURA syndrome research and understanding for our families” said Dominic J. Spadafore, the President of the Foundation.  “We expect that this will be the first of many grants.”
 

The clinical fellowship position has been awarded and the successful applicant is Dr Rebecca Mawby. Dr Mawby is a trainee Paediatrician with experience in complex paediatric disorders. She is continuing study in the area of epilepsy and seizures, and endocrinology, which will further benefit the PURA syndrome community. Dr Mawby will assist in the development of the global patient registry, completing research study from information gathered. She is expected to start in early September 2018.

 

 

For additional Information, please contact
PURA Syndrome Foundation President  
Dominic J. Spadafore
d.spadafore@pura-syndrome.org


Download Official Press Release

 

About the PURA Syndrome Foundation

The PURA Syndrome Foundation is a global organization, registered in the USA as a 501(c)(3) tax-exempt non-profit corporation. The PURA Syndrome Foundation supports and educates patients and their families, providing a global community. This community provides a place of belonging to those who may otherwise feel isolated by rare disease, enriches the medical research being completed and educates those outside the community about the condition. Their mission is to serve, educate and fund research for families coping with the effects of PURA syndrome. The foundation was established in 2016 and is registered in the United States.  The Foundation has board members in the EU, Australia, and the USA. The Foundation strives to bring together and support families across the globe.  To learn more, visit www.purasyndrome.org/

 

 

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The PURA Syndrome Foundation is a registered 501(c)(3) charity organization. Information on this website is not a substitute for personal medical advice. Families should consult a medically qualified physician in all matters relating to genetic diagnosis , management, and health . Information about PURA and genetics in general is a very fast moving area and while the information on this website is regarded as the best at the time of publication , some facts may change later .