International audienceSpinal muscular atrophy type 1 (SMA-1) is a severe neurodegenerative disorder, which in the absence of curative treatment, leads to death before 1 year of age in most cases. Caring for these short-lived and severely impaired infants requires palliative management. New drugs (nusinersen) have recently been developed that may modify SMA-1 natural history and thus raise ethical concerns about the appropriate level of care for patients. The national Hospital Clinical Research Program (PHRC) called "Assessment of clinical practices of palliative care in children with Spinal Muscular Atrophy Type 1 (SMA-1)" was a multicenter prospective study conducted in France between 2012 and 2016 to report palliative practices in SMA-1 i...
• NURTURE is an ongoing study of nusinersen started in a presymptomatic stage of SMA. ...
International audienceIntroduction: The recent development of disease-modifying treatments in spinal...
peer reviewedOBJECTIVE: To evaluate the safety and clinical efficacy of nusinersen in patients older...
International audienceSpinal muscular atrophy type 1 (SMA-1) is a severe neurodegenerative disorder,...
Background Spinal muscular atrophy (SMA) is one of the most common genetic causes of death in child...
Background: We report the clinical outcomes observed in our patients with SMA type 1 or 2 receiving ...
Introduction: Spinal muscular atrophy (SMA) is one of the most frequent autosomal recessive neuromus...
Introduction: Nusinersen, an antisense oligonucleotide designed to treat spinal muscular atrophy, le...
Objective To evaluate the safety and clinical efficacy of nusinersen in patients older than 7 months...
• NURTURE is an ongoing study of nusinersen started in a presymptomatic stage of SMA. ...
International audienceIntroduction: The recent development of disease-modifying treatments in spinal...
peer reviewedOBJECTIVE: To evaluate the safety and clinical efficacy of nusinersen in patients older...
International audienceSpinal muscular atrophy type 1 (SMA-1) is a severe neurodegenerative disorder,...
Background Spinal muscular atrophy (SMA) is one of the most common genetic causes of death in child...
Background: We report the clinical outcomes observed in our patients with SMA type 1 or 2 receiving ...
Introduction: Spinal muscular atrophy (SMA) is one of the most frequent autosomal recessive neuromus...
Introduction: Nusinersen, an antisense oligonucleotide designed to treat spinal muscular atrophy, le...
Objective To evaluate the safety and clinical efficacy of nusinersen in patients older than 7 months...
• NURTURE is an ongoing study of nusinersen started in a presymptomatic stage of SMA. ...
International audienceIntroduction: The recent development of disease-modifying treatments in spinal...
peer reviewedOBJECTIVE: To evaluate the safety and clinical efficacy of nusinersen in patients older...