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2018 SMA Researcher Meeting Summary: Basic Research Podium Presentations

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The SMA Researcher Meeting is the largest research meeting in the world specifically focused on SMA and seeks to create open communication of early, unpublished […]

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2018 SMA Researcher Meeting Special Session Summary: Clinical and Basic Questions of SMA in the Era of SMN Repletion: Challenge and Opportunity

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The SMA Researcher Meeting is the largest research meeting in the world specifically focused on SMA and seeks to create open communication of early, unpublished […]

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Cure SMA Awards $300,000 Grant to Kevin Hodgetts, PhD, The Brigham and Women’s Hospital

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Cure SMA has awarded a $300,000 preclinical drug discovery grant to Kevin Hodgetts, PhD, at the Brigham and Women’s Hospital, for his project, ” Pre-Clinical […]

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Cure SMA Awards $300,000 Grant to Umrao Monani, PhD, Columbia University

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Cure SMA has awarded a $300,000 preclinical drug discovery grant to Umrao Monani, PhD, at Columbia University, for his project, ” Restoring function at the […]

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HHS Secretary, Alex Azar, Recommends Nationwide Newborn Screening for SMA

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Health and Human Services Secretary Alex Azar today approved the recommendation that newborn screening for spinal muscular atrophy be implemented nationwide. This recommendation was issued […]

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Thank You For a Wonderful 2018 Annual SMA Conference!

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Thank you to everyone who attended the 2018 Annual SMA Conference at the Hilton Anatole Hotel in Dallas, Texas! It was an impactful weekend of […]

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Biogen to Present New Data at the 2018 Annual SMA Conference

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Yesterday, Biogen announced it will present data from its SPINRAZA clinical development program –the largest of its kind, with more than six years of data–for […]

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Spring 2018 Issue of Directions Now Available

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The Spring 2018 issue of Directions is now available online. Check out our Support & Care publications page to download past issues of Directions and […]

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Indiana Becomes Fourth State to Adopt Newborn Screening for Spinal Muscular Atrophy

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On Friday, Governor Eric Holcomb held a signing ceremony for Indiana House Bill 1017, adopting newborn screening for spinal muscular atrophy (SMA) and severe combined […]

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Uniting the SMA Community Through Local Programs and Support

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After her son William’s SMA type 2 diagnosis in April 2001, Heidi Johnson’s doctor immediately showed her the Cure SMA (then Families of SMA) website […]

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