Scaling parent management training through digital and microlearning approaches

por Grodberg, David, Smith, Irene
Publicado 2022

Feasibility and Acceptability of Delivering Pivotal Response Treatment for Autism Spectrum Disorder via Telehealth: Pilot Pre-Post Study

por Drapalik, Krista N, Grodberg, David, Ventola, Pamela
Publicado 2022

Clinical and Psychosocial Outcomes Associated With a Tele-behavioral Health Platform for Families: Retrospective Study

por Loo, Theoren, Hunt, Justin, Grodberg, David, Bravata, Dena
Publicado 2023

Examining the Relationship Between Pediatric Behavioral Health and Parent Productivity Through a Parent-Reported Survey in the Time of COVID-19: Exploratory Study

por Grodberg, David, Bridgewater, Jesse, Loo, Theoren, Bravata, Dena
Publicado 2022

A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome

por Kolevzon, Alexander, Bush, Lauren, Wang, A Ting, Halpern, Danielle, Frank, Yitzchak, Grodberg, David, Rapaport, Robert, Tavassoli, Teresa, Chaplin, William, Soorya, Latha, Buxbaum, Joseph D
Publicado 2014

Erratum: A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome

por Kolevzon, Alexander, Bush, Lauren, Wang, A Ting, Halpern, Danielle, Frank, Yitzchak, Grodberg, David, Rapaport, Robert, Tavassoli, Teresa, Chaplin, William, Soorya, Latha, Buxbaum, Joseph D
Publicado 2015

De novo SCN2A splice site mutation in a boy with Autism spectrum disorder

por Tavassoli, Teresa, Kolevzon, Alexander, Wang, A Ting, Curchack-Lichtin, Jocelyn, Halpern, Danielle, Schwartz, Lily, Soffes, Sarah, Bush, Lauren, Grodberg, David, Cai, Guiqing, Buxbaum, Joseph D
Publicado 2014

Functional deficits of the attentional networks in autism

por Fan, Jin, Bernardi, Silvia, Dam, Nicholas T, Anagnostou, Evdokia, Gu, Xiaosi, Martin, Laura, Park, Yunsoo, Liu, Xun, Kolevzon, Alexander, Soorya, Latha, Grodberg, David, Hollander, Eric, Hof, Patrick R
Publicado 2012

Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency

por Soorya, Latha, Kolevzon, Alexander, Zweifach, Jessica, Lim, Teresa, Dobry, Yuriy, Schwartz, Lily, Frank, Yitzchak, Wang, A Ting, Cai, Guiqing, Parkhomenko, Elena, Halpern, Danielle, Grodberg, David, Angarita, Benjamin, Willner, Judith P, Yang, Amy, Canitano, Roberto, Chaplin, William, Betancur, Catalina, Buxbaum, Joseph D
Publicado 2013