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Pierre Fabre e la Fondazione EspeRare avviano lo studio clinico EDELIFE su un trattamento prenatale per una rara malattia genetica, la XLHED
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Fundación EspeRare recibe el apoyo de Duchenne Parent Project España para iniciar en Barcelona el primer ensayo europeo en la seguridad clínica de Rimeporide en pacientes con distrofia muscular de Duchenne -
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11 pediatric cardiovascular devices you need to know - Page 8 of 11 - Medical Design and Outsourcing
Patient Recruitment and Retention for Rare Disease Clinical Trials Remains a Hurdle - Clinical Trials Arena
EDI-200: Drug Targets, Indications, Patents - Synapse
Rarity Life Issue 6 by Rarity Life - Issuu
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EspeRare foundation Email Format | esperare.org Emails
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Caroline Kant email address & phone number | EspeRare foundation Co-Founder & CEO contact information - RocketReach
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Caroline Kant email address & phone number | EspeRare foundation Co-Founder & CEO contact information - RocketReach
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EspeRare Foundation - BioAlps
NFED Leader Celebrates 20 Year Anniversary | NFED
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Pierre Fabre on X: "The EspeRare Foundation and #PierreFabre join forces to develop and market a pioneering treatment for XLHED, a dermatological ultrarare genetic disease that requires prenatal therapeutic intervention. https://t.co/Kapqvu4RpT #Health #