Simons Searchlight — Biomedical Watch V2

Traitements2programmes

Essais1liés

Publications0liées

SourceDBlocale

Traitements

2

Molécule	Indication / population	Phase	Objectif	Pays	Résultat
Online Study of People Who Have Genetic Changes and Features of Autism: Simons SearchlightSimons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment for these people. Simons Searchlight partners with families to collect data and distribute it to qualified researchers.	Épilepsie	À vérifier	À vérifier	United States	À vérifier
Online Study of People Who Have Genetic Changes and Features of Autism: Simons SearchlightSimons Searchlight is an observational, online, international research program for families with rare genetic variants that cause neurodevelopmental disorders and may be associated with autism. Simons Searchlight collects medical, behavioral, learning, and developmental information from people who have these rare genetic changes. The goal of this study is to improve the clinical care and treatment for these people. Simons Searchlight partners with families to collect data and distribute it to qualified researchers.	Épilepsie	À vérifier	À vérifier	United States	À vérifier

Essais cliniques

1

Molécule	Indication / population	Phase	NCT	Titre	Statut
Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight	Épilepsie	À vérifier	NCT01238250	Online Study of People Who Have Genetic Changes and Features of Autism: Simons Searchlight	RECRUITING

Publications

0

Molécule	Indication / population	Titre	Journal	Date
Aucune publication.