Human-specific microglial Siglec-11 transcript variant has the potential to affect polysialic acid-mediated brain functions at a distance von Hane, Masaya, Chen, Dillon Y, Varki, Ajit

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Glucocorticoid receptors recruit the CaMKIIα-BDNF-CREB pathways to mediate memory consolidation von Chen, Dillon Y, Bambah-Mukku, Dhananjay, Pollonini, Gabriella, Alberini, Cristina M

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Memory enhancement: consolidation, reconsolidation and insulin-like growth factor 2 von Alberini, Cristina M, Chen, Dillon Y

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A positive autoregulatory BDNF feedback loop via C/EBPβ mediates hippocampal memory consolidation von Bambah-Mukku, Dhananjay, Travaglia, Alessio, Chen, Dillon Y, Pollonini, Gabriella, Alberini, Cristina M

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Tumor-related epilepsy: epidemiology, pathogenesis and management von Chen, Dillon Y., Chen, Clark C., Crawford, John R., Wang, Sonya G.

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Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly von Wang, Lu, Li, Zhen, Sievert, David, Smith, Desirée E. C., Mendes, Marisa I., Chen, Dillon Y., Stanley, Valentina, Ghosh, Shereen, Wang, Yulu, Kara, Majdi, Aslanger, Ayca Dilruba, Rosti, Rasim O., Houlden, Henry, Salomons, Gajja S., Gleeson, Joseph G.

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Improved methods to characterize the length and quantity of highly unstable PolySialic acids subject category: (Carbohydrates, chromatographic techniques) von Vaill, Michael, Chen, Dillon Y., Diaz, Sandra, Varki, Ajit

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A critical role for IGF-II in memory consolidation and enhancement von Chen, Dillon Y., Stern, Sarah A., Garcia-Osta, Ana, Saunier-Rebori, Bernadette, Pollonini, Gabriella, Bambah-Mukku, Dhananjay, Blitzer, Robert D., Alberini, Cristina M.

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Restricted diffusion of the callosal splenium is highly specific for seizures in neonates von Nguyen, Linda, Chen, Dillon Y, Vinocur, Daniel N, Gold, Jeffrey J

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The Effect of Insulin and Insulin-Like Growth Factors on Hippocampus- and Amygdala-Dependent Long-Term Memory Formation von Stern, Sarah A, Chen, Dillon Y, Alberini, Cristina M

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Sonography of musculoskeletal soft-tissue masses: techniques, pearls, and pitfalls von Carra, Bradley J, Bui-Mansfield, Liem T, O'Brien, Seth D, Chen, Dillon C

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Lysosomal cholesterol accumulation contributes to the movement phenotypes associated with NUS1 haploinsufficiency von Yu, Seok-Ho, Wang, Tong, Wiggins, Kali, Louie, Raymond J., Merino, Emilio F., Skinner, Cindy, Cassera, Maria B., Meagher, Kirsten, Goldberg, Paul, Rismanchi, Neggy, Chen, Dillon, Lyons, Michael J., Flanagan-Steet, Heather, Steet, Richard

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Imaging Features of Soft-Tissue Calcifications and Related Diseases: A Systematic Approach von Hwang, Zhen-An, Suh, Kyung Jin, Chen, Dillon, Chan, Wing P, Wu, Jim S

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Author Correction: Loss of NARS1 impairs progenitor proliferation in cortical brain organoids and leads to microcephaly von Wang, Lu, Li, Zhen, Sievert, David, Smith, Desirée E. C., Mendes, Marisa I., Chen, Dillon Y., Stanley, Valentina, Ghosh, Shereen, Wang, Yulu, Kara, Majdi, Aslanger, Ayca Dilruba, Rosti, Rasim O., Houlden, Henry, Salomons, Gajja S., Gleeson, Joseph G.

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Osteochondroma-like parosteal osteosarcoma: A case highlighting diagnostic challenge and surgical advances von Majd, Naveed, Theriault, Raminta V., Darrow, Morgan A., Thorpe, Steven W., Chen, Dillon C.

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Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism von Wenderski, Wendy, Wang, Lu, Krokhotin, Andrey, Walsh, Jessica J., Li, Hongjie, Shoji, Hirotaka, Ghosh, Shereen, George, Renee D., Miller, Erik L., Elias, Laura, Gillespie, Mark A., Son, Esther Y., Staahl, Brett T., Baek, Seung Tae, Stanley, Valentina, Moncada, Cynthia, Shipony, Zohar, Linker, Sara B., Marchetto, Maria C. N., Gage, Fred H., Chen, Dillon, Sultan, Tipu, Zaki, Maha S., Ranish, Jeffrey A., Miyakawa, Tsuyoshi, Luo, Liqun, Malenka, Robert C., Crabtree, Gerald R., Gleeson, Joseph G.

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Rapid Diagnosis of KCNQ2-Associated Early Infantile Epileptic Encephalopathy Improved Outcome von Chen, Dillon Y., Chowdhury, Shimul, Farnaes, Lauge, Friedman, Jennifer R., Honold, Jose, Dimmock, David P., Gold, on behalf of the RCIGM investigators, Jeffrey J.

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Bi-allelic Loss of Human APC2, Encoding Adenomatous Polyposis Coli Protein 2, Leads to Lissencephaly, Subcortical Heterotopia, and Global Developmental Delay von Lee, Sangmoon, Chen, Dillon Y., Zaki, Maha S., Maroofian, Reza, Houlden, Henry, Di Donato, Nataliya, Abdin, Dalia, Morsy, Heba, Mirzaa, Ghayda M., Dobyns, William B., McEvoy-Venneri, Jennifer, Stanley, Valentina, James, Kiely N., Mancini, Grazia M.S., Schot, Rachel, Kalayci, Tugba, Altunoglu, Umut, Karimiani, Ehsan Ghayoor, Brick, Lauren, Kozenko, Mariya, Jamshidi, Yalda, Manzini, M. Chiara, Beiraghi Toosi, Mehran, Gleeson, Joseph G.

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The Half-Moon Sign of the Femoral Neck Is Nonspecific for the Diagnosis of Osteoid Osteoma von Carra, Bradley J, Chen, Dillon C, Bui-Mansfield, Liem T

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Novel CNTNAP1 gene variant identified in congenital hypomyelinating neuropathy-3: A case report von Wang, Helen, Chen, Dillon, Del Campo, Miguel, Del Rosario, Pamela, Lee, Pei-Shan

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