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Town and Gown 10k event set for 42nd year in Oxford

Muscular Dystrophy UK has announced it s fundraising 10k event will be coming back to Oxford for a 42nd year.

United kingdomAlistair blackmoreDaniel cleaverJessie keighleyBidwells oxfordOxford neuromuscular centreCollege teamUniversity of oxfordMuscular dystrophy united kingdomBidwells townOxford townMuscular dystrophy unitedNew college teamNeuromuscular centre

These little girls were born with the same cruel genetic illness but baby Amelia will never suffer like big sister Maisie - thanks to a miracle £75,000-a-dose jab

Portia Thorman of the Spinal Muscular Atrophy charity SMA, said these new treatments were not available when her son Ezra, pictured left, was born.

United kingdomPortia thormanSinead connollyLaurent servaisElizabeth wraigeUnited kingdom national screening committeeLiege universityOxford neuromuscular centreNational screening committeeSpinal muscular atrophyEvelina london childrenProfessor laurent servaisProf servais

New Advancement Toward The First Primary Endpoint Qualification Of A Digital Endpoint For Duchenne

Current methods for assessing ambulatory function in patients with Duchenne muscular dystrophy do not fully reflect how they experience DMD in their.

Region flamandeBruxelles capitaleFrance generalRobert debrRoxana donisa dreghiciLaurent servaisCarl morrisDonisa dreghiciHead of clinical developmentLouvain medical schoolNovo nordiskFranklin pierce collegeUniversity of medicineDepartment of physiologyEuropean medicines agencyInstitute of myology

New Four-Year Data for Genentech s Evrysdi Reinforce Long-Term Efficacy and Safety Profile in Some of the Most Severely Affected People With Types 2 and 3 Spinal Muscular Atrophy (SMA) Seite 1

20.03.2023 - Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX: RHHBY), today announced new long-term data for Evrysdi (risdiplam) in a broad range of people aged 2-25 years with spinal muscular atrophy (SMA) from the pivotal SUNFISH study. Data . Seite 1

Laurent servaisLevi garrawayMuscular dystrophy associationRoche groupGlobal product developmentOxford neuromuscular centreScientific conferencePaediatric neuromuscular diseasesMotor functionRevised upper limb moduleGlobal productRoche holding

F Hoffmann-La Roche Ltd: New four year data for Roche s Evrysdi reinforce long-term efficacy and safety profile in some of the most severely affected people with types 2 and 3 spinal muscular atrophy (SMA)

Data from pivotal SUNFISH study showed increases in motor function observed during the first year were maintained through the fourth year, while the overall rate of adverse events continued to decrease

United statesUnited kingdomLevi garrawaySabine borngrGerard tobinBruno eschliLaurent servaisBirgit masjostLoren kalmNathalie altermattMuscular dystrophy associationSociety for medicines researchToddler developmentBritish pharmacological societyDrug administrationHead of global product development

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