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#RareShowcase23: Thiloka Ratnaike, Mitochondrial diseases: can we improve diagnosis for patients?

Duration: 5:03

#RareShowcase23 Catriona Crombie - Challenges to translating rare disease research into impact

Duration: 10:34

#RareShowcase23: Fiona Nielsen, Challenges of drug discovery for rare developmental diseases

Duration: 6:35

#RareShowcase23: Mel Dixon, Navigating our way through the labyrinth of a newly discovered disease

Duration: 4:42

#RareShowcase23 Prof. Heinz Jungbluth - Rare disease research: the Paediatric Neurology perspective

Duration: 18:56

#RareShowcase23 Richard Evans - MRC-NIHR rare diseases research platform and MRC funding

Duration: 19:00

#RareShowcase23 Lightning Talk Loren Cameron - Inequality and diversity in clinical research

Duration: 5:43

#RareShowcase23: Paul Wicks, Lessons learned from the other side of the desk in genetic testing

Duration: 5:43

#RareShowcase23 Lightning Talk Esme Down - A medical student with rare diseases

Duration: 4:46

#RareShowcase23: Kirsty Hoyle, Thoughts into Action

Duration: 4:57

#RareShowcase23 Addassa Follett - Empowering lives: the Sickle Cell Society's Impact

Duration: 14:30

#RareShowcase23 Lightning Talk Lara Bloom - How project ECHO can help rare diseases

Duration: 5:38

#RareShowcase23 Nick Meade, Genetic Alliance UK - The future of rare advocacy in UK Parliaments

Duration: 14:57

#RareShowcase23 Melita Irving, Guy's and St Thomas' - Trials and tribulations in rare diseases

Duration: 17:05

#RareShowcase23 Lightning Talk Dr Will Evans - Stratifying patients for rare disease identification

Duration: 5:15

#RareShowcase23 David Rose - Lived experiences of being a GOSH patient and volunteer

Duration: 16:13

#RareShowcase23 Lightning Talk Allison Watson - UKRET: the power of collaboration in rare disease

Duration: 5:08

#RareShowcase23 Lightning Talk Michelle Conway and Lorna Pender - Navigating early access programs

Duration: 5:31

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