Matthew F. Pescosolido
Affiliations: | 2013- | Neuroscience | Brown University, Providence, RI |
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| Kavanaugh BC, Elacio J, Best CR, et al. (2023) Christianson Syndrome across the Lifespan: An International Longitudinal Study in Children, Adolescents, and Adults. Medrxiv : the Preprint Server For Health Sciences |
| Pescosolido MF, Ouyang Q, Liu JS, et al. (2023) Live-Imaging Detection of Multivesicular Body-Plasma Membrane Fusion and Exosome Release in Cultured Primary Neurons. Methods in Molecular Biology (Clifton, N.J.). 2683: 213-220 |
| Pescosolido MF, Ouyang Q, Liu JS, et al. (2021) Loss of Christianson Syndrome Na+/H+ Exchanger 6 () Causes Abnormal Endosome Maturation and Trafficking Underlying Lysosome Dysfunction in Neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience |
| Lizarraga SB, Ma L, Maguire AM, et al. (2021) Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategies. Science Translational Medicine. 13 |
| Pescosolido MF, Kavanaugh BC, Pochet N, et al. (2019) Complex Neurological Phenotype in Female Carriers of Mutations. Molecular Neuropsychiatry. 5: 98-108 |
| Pruett B, Pescosolido M, Best C, et al. (2018) F46. Brain MRI Morphometry Changes Associated With Na+/H+ Exchanger 6 (NHE6) Mutations in Christianson Syndrome (CS) Biological Psychiatry. 83: S255 |
| Xu M, Ouyang Q, Gong J, et al. (2017) Mixed Neurodevelopmental and Neurodegenerative Pathology in Nhe6-Null Mouse Model of Christianson Syndrome. Eneuro. 4 |
| Gamsiz ED, Sciarra LN, Maguire AM, et al. (2015) Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 12: 553-71 |
| Pescosolido MF, Schwede M, Johnson Harrison A, et al. (2014) Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein. Journal of Medical Genetics. 51: 587-9 |
| Pescosolido MF, Stein DM, Schmidt M, et al. (2014) Genetic and phenotypic diversity of NHE6 mutations in Christianson syndrome. Annals of Neurology. 76: 581-93 |