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RARE News
RARE News
The CMT Research Foundation’s 2024 Global CMT Research Convention to gather renowned scientific experts and patients to discuss status of treatments and cures for Charcot-Marie-Tooth (CMT) disease
By admin
19 July 2024
RARE News
NHL All-Star Ryan Getzlaf returns to the links for the 13th Annual Getzlaf Golf Shootout on September 13-14, benefiting CureDuchenne
By admin
17 July 2024
Industry Insights
Early access to medicines: A picture is worth a thousand words
By CONTRIBUTOR
17 July 2024
RARE News
Challenges and priorities for the PSP and CBD community: Insights from Mark Jackson
By admin
12 July 2024
RARE News
The CMT Research Foundation to launch grant program to support young investigators working on CMT
By admin
12 July 2024
Charity & advocacy
Bridging gaps in care: How independent charitable patient assistance organisations support underserved populations
By CONTRIBUTOR
10 July 2024
RARE News
Concerned stakeholders issue call to action on the implementation of the EU Joint Clinical Assessment for ATMPs
By admin
9 July 2024
Industry Insights
What can rare disease services learn from oncology services? A personal reflection
By CONTRIBUTOR
1 July 2024
RARE News
International Neonatal Screening Day: A call for global implementation of neonatal screening programmes
By admin
28 June 2024
RARE News
PSPA event brings together families affected by progressive supranuclear palsy and corticobasal degeneration
By admin
25 June 2024
Letters
“Glass siblings”: an unnecessary label
By CONTRIBUTOR
24 June 2024
RARE News
Little Moments Matter: a new film from Dravet Syndrome UK marks Dravet Syndrome Awareness Day
By admin
24 June 2024
Turning the tide for rare disease
The UK General Election 2024: Ensuring rare diseases remain a priority
By CONTRIBUTOR
24 June 2024
RARE caregiving
A road less travelled is no less worthy: A RARE mum’s reflections on special needs parenting
By CONTRIBUTOR
21 June 2024
RARE News
Cure GABA-A: A year of transformative impact in the GABAAR community
By admin
20 June 2024
RARE News
American Kidney Fund convenes Rare Kidney Disease Action Network to advocate change for patients with rare causes of kidney disease
By admin
18 June 2024
Charity & advocacy
A day in the life: Being diagnosed with Fanconi anaemia as a child and as an adult—what are the differences?
By CONTRIBUTOR
18 June 2024
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