Lighting a path: genetic studies pinpoint neurodevelopmental mechanisms in autism and related disorders

por Pescosolido, Matthew F., Yang, Unikora, Sabbagh, Mark, Morrow, Eric M.
Publicado 2012

Loss of Christianson Syndrome Na(+)/H(+) Exchanger 6 (NHE6) Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons

por Pescosolido, Matthew F., Ouyang, Qing, Liu, Judy S., Morrow, Eric M.
Publicado 2021

Clinical Characteristics of Children with Autism Spectrum Disorder and Co-Occurring Epilepsy

por Viscidi, Emma W., Triche, Elizabeth W., Pescosolido, Matthew F., McLean, Rebecca L., Joseph, Robert M., Spence, Sarah J., Morrow, Eric M.
Publicado 2013

Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein

por Pescosolido, Matthew F, Schwede, Matthew, Johnson Harrison, Ashley, Schmidt, Michael, Gamsiz, Ece D, Chen, Wendy S, Donahue, John P, Shur, Natasha, Jerskey, Beth A, Phornphutkul, Chanika, Morrow, Eric M
Publicado 2014

Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome

por Xu, Meiyu, Ouyang, Qing, Gong, Jingyi, Pescosolido, Matthew F., Pruett, Brandon S., Mishra, Sasmita, Schmidt, Michael, Jones, Richard N., Gamsiz Uzun, Ece D., Lizarraga, Sofia B., Morrow, Eric M.
Publicado 2018