Consensus Statement for Standard of Care in Spinal Muscular Atrophy
By Ching H. Wang, R. Finkel, E. Bertini, M. Schroth, A. Simonds, B. Wong, A. Aloysius, L. Morrison, M. Main, T. Crawford and 1 more. Journal of Child Neurology, 2007
867 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Genetics, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/1cc492691f66017a845f2c0307e22fe216911daf
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Citations in the corpus
- Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care. (2017, positive): “A literature search identified all the relevant articles that were classified according to their consistency with the previous recommendations [3], or whether they included novel or contrasting findings.”
- Antisense correction of SMN2 splicing in the CNS rescues necrosis in a type III SMA mouse model. (2010, background): “There are three types of childhood-onset SMA, based on the severity and the time of onset: Type I is most severe, and type III is a mild form (Munsat and Davies 1992; Crawford 2003; Russman 2007; Wang et al. 2007).”
- Single‐Dose Gene‐Replacement Therapy for Spinal Muscular Atrophy (2017, neutral): “Viral upper respiratory tract infection 0 0 3 3 (25) 3 3 (20)”