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A telehealth approach to improving clinical trial access for infants with tuberous sclerosis complex

BACKGROUND: Research in rare genetic syndromes associated with ASD is often hampered by the wide geographic distribution of families and the presence of medical comorbidities, such as epilepsy, that may preclude travel to clinical sites. These challenges can limit the sample size and generalizabilit...

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Detaylı Bibliyografya
Yayımlandı:J Neurodev Disord
Asıl Yazarlar: Hyde, Carly, Pizzano, Maria, McDonald, Nicole M., Nelson, Charles A., Kasari, Connie, Thiele, Elizabeth A., Jeste, Shafali S.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6977334/
https://ncbi.nlm.nih.gov/pubmed/31969108
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s11689-019-9302-0
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