Differential Gaze Patterns on Eyes and Mouth During Audiovisual Speech Segmentation

por Lusk, Laina G., Mitchel, Aaron D.
Publicado 2016

Concomitant Calcium Channelopathies Involving CACNA1A and CACNA1F: A Case Report and Review of the Literature

por Schaare, Donna, Sarasua, Sara M., Lusk, Laina, Parthasarathy, Shridhar, Wang, Liangjiang, Helbig, Ingo, Boccuto, Luigi
Publicado 2023

Social cognition, face processing, and oxytocin receptor single nucleotide polymorphisms in typically developing children

por Slane, Mylissa M., Lusk, Laina G., Boomer, K.B., Hare, Abby E., King, Margaret K., Evans, David W.
Publicado 2014

Multisite Semiautomated Clinical Data Repository for Duplication 15q Syndrome: Study Protocol and Early Uses

por Ajayi, Oluwaseun Jessica, Smith, Ebony Jeannae, Viangteeravat, Teeradache, Huang, Eunice Y, Nagisetty, Naga Satya V Rao, Urraca, Nora, Lusk, Laina, Finucane, Brenda, Arkilo, Dimitrios, Young, Jennifer, Jeste, Shafali, Thibert, Ronald, Reiter, Lawrence T
Publicado 2017

Intrafamilial variability in SLC6A1-related neurodevelopmental disorders

por Kassabian, Benedetta, Fenger, Christina Dühring, Willems, Marjolaine, Aledo-Serrano, Angel, Linnankivi, Tarja, McDonnell, Pamela Pojomovsky, Lusk, Laina, Jepsen, Birgit Susanne, Bayat, Michael, Kattentidt-Mouravieva, Anja A., Vidal, Anna Abulí, Valero-Lopez, Gabriel, Alarcon-Martinez, Helena, Goodspeed, Kimberly, van Slegtenhorst, Marjon, Barakat, Tahsin Stefan, Møller, Rikke S., Johannesen, Katrine M., Rubboli, Guido
Publicado 2023

Corrigendum: Intrafamilial variability in SLC6A1-related neurodevelopmental disorders

por Kassabian, Benedetta, Fenger, Christina Dühring, Willems, Marjolaine, Aledo-Serrano, Angel, Linnankivi, Tarja, McDonnell, Pamela Pojomovsky, Lusk, Laina, Jepsen, Birgit Susanne, Bayat, Michael, Kattentidt-Mouravieva, Anja A., Vidal, Anna Abulí, Valero-Lopez, Gabriel, Alarcon-Martinez, Helena, Goodspeed, Kimberly, van Slegtenhorst, Marjon, Barakat, Tahsin Stefan, Møller, Rikke S., Johannesen, Katrine M., Rubboli, Guido
Publicado 2023

Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature

por Priestley, Jessica R.C., Pace, Lisa M., Sen, Kuntal, Aggarwal, Anjali, Alves, Cesar Augusto P.F., Campbell, Ian M., Cuddapah, Sanmati R., Engelhardt, Nicole M., Eskandar, Marina, Jolín García, Paloma C., Gropman, Andrea, Helbig, Ingo, Hong, Xinying, Gowda, Vykuntaraju K., Lusk, Laina, Trapane, Pamela, Srinivasan, Varunvenkat M., Suwannarat, Pim, Ganetzky, Rebecca D.
Publicado 2022