Improved Diabetes Control and Pancreatic Function in a Type 2 Diabetic after Omeprazole Administration von Mefford, I. N., Mefford, J. T., Burris, C. A.

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Genetic generalized epilepsies von Mullen, Saul A., Berkovic, Samuel F., Berkovic, Samuel F, Lowenstein, Daniel H, Kato, Mitsuhiro, Cross, Helen, Satishchandra, Parthasathy, Jonghe, Peter, Goldman, Alica, Petrou, Steve, Tan, Nigel CK, Helbig, Ingo, Mefford, Heather C, Jiang, Yuwu

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Cerebrospinal fluid monoamine metabolites in boys with attention-deficit hyperactivity disorder von Castellanos, F.Xavier, Elia, Josephine, Kruesi, Markus J.P., Gulotta, Charles S., Mefford, Ivan N., Potte, William Z., Ritchie, Gail F., Rapoport, Judith L.

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De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies von Myers, Candace T., McMahon, Jacinta M., Schneider, Amy L., Petrovski, Slavé, Allen, Andrew S., Carvill, Gemma L., Zemel, Matthew, Saykally, Julia E., LaCroix, Amy J., Heinzen, Erin L., Hollingsworth, Georgina, Nikanorova, Marina, Corbett, Mark, Gecz, Jozef, Coman, David, Freeman, Jeremy, Calvert, Sophie, Gill, Deepak, Carney, Patrick, Lerman-Sagie, Tally, Sampaio, Hugo, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E., Epstein, Michael P., Glauser, Tracy, Johnson, Michael R., Kuzniecky, Ruben, Marson, Anthony G., O’Brien, Terence J., Ottman, Ruth, Petrou, Stephen, Poduri, Annapurna, Pickrell, William O., Chung, Seo-Kyung, Rees, Mark I., Sherr, Elliott, Sadleir, Lynette G., Goldstein, David B., Lowenstein, Daniel H., Møller, Rikke S., Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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The ClinGen Brain Malformation Variant Curation Expert Panel: Rules for somatic variants in AKT3, MTOR, PIK3CA, and PIK3R2 von Lai, Abbe, Soucy, Aubrie, El Achkar, Christelle Moufawad, Barkovich, Anthony J., Cao, Yang, DiStefano, Marina, Evenson, Michael, Guerrini, Renzo, Knight, Devon, Lee, Yi-Shan, Mefford, Heather C., Miller, David T., Mirzaa, Ghayda, Mochida, Ganesh, Rodan, Lance H., Patel, Mayher, Smith, Lacey, Spencer, Sara, Walsh, Christopher A., Yang, Edward, Yuskaitis, Christopher J., Yu, Timothy, Poduri, Annapurna, Achkar, Christelle, Barkovich, James, Cao, Yang, Chelly, Jamel, DiStefano, Marina, Engle, Elizabeth, Evenson, Michael, Guerrini, Renzo, Hong, William, Koh, Hyunyong, Knight, Devon, Lai, Abbe, Lassiter, Rhonda, Lee, Yi-Shan, Marsh, Eric, Mefford, Heather C., Miller, David T., Mirzaa, Ghayda, Mochida, Ganesh, Pinsky, Rebecca, Poduri, Annapurna, Rodan, Lance H., Patel, Mayher, Shain, Catherine, Smith, Lacey, Soucy, Aubrie, Spencer, Sara, Walsh, Christopher A., Yang, Edward, Yu, Timothy, Yuan, Bo, Yuskaitis, Christopher

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Quantitative Examination of Tissue Concentration Profiles Associated with Microdialysis von Dykstra, Kevin H., Hsiao, John K., Morrison, Paul F., Bungay, Peter M., MefFord, Ivan N., Scully, Melinda M., Dedrick, Robert L.

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Quantitative Microdialysis: Analysis of Transients and Application to Pharmacokinetics in Brain von Morrison, Paul F., Bungay, Peter M., Hsiao, John K., Ball, Beth A., Mefford, Ivan N., Dedrick, Robert L.

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Genetic literacy series: genetic epilepsy with febrile seizures plus von Myers, Kenneth A., Scheffer, Ingrid E., Berkovic, Samuel F.

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Neurodevelopmental copy-number variants: A roadmap to improving outcomes by uniting patient advocates, researchers, and clinicians for collective impact von Buttermore, Elizabeth, Chamberlain, Stormy, Cody, Jannine, Costain, Gregory, Dang, Louis, DeWoody, Andrew, DeWoody, Yssa, Dies, Kira, Eichler, Evan, Girirajan, Santhosh, Gramm, Marie, Halladay, Alycia, Lal, Dennis, Lalli, Matthew, Levy, Tess, Logsdon, Glennis, Lowenstein, Daniel, Mefford, Heather, Mulle, Jennifer, Muotri, Alysson, Murphy, Melissa, Perez Palma, Eduardo, Pinter, Stefan, Pollak, Rebecca, Purcell, Ryan, Samaco, Rodney, Shah, Bina, Singh, Karun, So, Joyce, Sundberg, Maria, Veeraragavan, Surabi, Vogel-Farley, Vanessa, Wynshaw-Boris, Anthony

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Hippocampal 8‐[3H]Hydroxy‐2‐(Di‐n‐Propylamino)Tetralin Binding Site Densities, Serotonin Receptor (5‐HT1A) Messenger Ribonucleic Acid Abundance, and Serotonin Levels Parallel the A... von Burnet, Philip W. J., Mefford, Ivan N., Smith, Craig C., Gold, Philip W., Sternberg, Esther M.

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ILAE Genetics Literacy series: Progressive myoclonus epilepsies von Cameron, Jillian M, Ellis, Colin A, Berkovic, Samuel F

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ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy von Millevert, Charissa, Weckhuysen, Sarah, Perucca, Piero, Cross, J. Helen, Lerche, Holger, Esterhuizen, Alina I., Lopes‐Cendes, Iscia, Tsai, Meng‐Han, Berkovic, Samuel F., Lowenstein, Daniel H., Tan, Nigel C. K., Helbig, Ingo, Mefford, Heather C., Brunklaus, Andreas, Lesca, Gaetan

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Epi4K: Gene discovery in 4,000 genomes

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ILAE Genetic Literacy Series: Postmortem Genetic Testing in Sudden Unexpected Death in Epilepsy von Bagnall, Richard D., Perucca, Piero, Cross, J. Helen, Lerche, Holger, Esterhuizen, Alina I., Lopes‐Cendes, Iscia, Tsai, Meng‐Han, Berkovic, Samuel F., Lowenstein, Daniel H., Tan, Nigel C. K., Helbig, Ingo, Mefford, Heather C., Brunklaus, Andreas, Lesca, Gaetan

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Diverse genetic causes of polymicrogyria with epilepsy von Allen, Andrew S, Aggarwal, Vimla, Berkovic, Samuel F, Cossette, Patrick, Delanty, Norman, Dlugos, Dennis, Eichler, Evan E, Epstein, Michael P, Freyer, Catharine, Goldstein, David B, Guerrini, Renzo, Glauser, Tracy, Heinzen, Erin L, Johnson, Michael R, Kuzniecky, Ruben, Lowenstein, Daniel H, Marson, Anthony G, Mefford, Heather C, O'Brien, Terence J, Ottman, Ruth, Poduri, Annapurna, Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K, Scheffer, Ingrid E, Sherr, Elliott H, Abou‐Khalil, Bassel, Amrom, Dina, Andermann, Eva, Andermann, Frederick, Berkovic, Samuel F., Bluvstein, Judith, Boro, Alexis, Cascino, Greg, Consalvo, Damian, Crumrine, Pat, Devinsky, Orrin, Dlugos, Dennis, Fountain, Nathan, Freyer, Catharine, Friedman, Dan, Geller, Eric, Glynn, Simon, Haas, Kevin, Haut, Sheryl, Joshi, Sucheta, Kirsch, Heidi, Knowlton, Robert, Kossoff, Eric, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack M., Poduri, Annapurna, Scheffer, Ingrid, Shellhaas, Renée A., Sherr, Elliott H., Shih, Jerry J., Shinnar, Shlomo, Singh, Rani K., Sperling, Michael, Smith, Michael C., Sullivan, Joseph, Vining, Eileen P. G., Von Allmen, Gretchen K., Widdess‐Walsh, Peter, Winawer, Melodie R., Bautista, Jocelyn, Fiol, Miguel, Glauser, Tracy, Hayward, Jean, Helmers, Sandra, Park, Kristen, Sirven, Joseph, Lin Thio, Liu, Venkat, Anu, Weisenberg, Judith, Kuperman, Rachel, McGuire, Shannon, Novotny, Edward, Sadleir, Lynette

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ILAE genetic literacy series: Focal cortical dysplasia von Macdonald-Laurs, Emma, Leventer, Richard J

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Effects of Different Semipermeable Membranes on In Vitro and In Vivo Performance of Microdialysis Probes von Hsiao, John K., Ball, Beth Ann, Morrison, Paul F., Mefford, Ivan N., Bungay, Peter M.

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Facile oxidative decarboxylation of 3,4-dihydroxyphenylacetic acid catalyzed by copper and manganese ions von Mefford, Ivan N., Kincl, Laurel, Dykstra, Kevin H., Simpson, John T., Markey, Sanford P., Dietz, Susanne, Wightman, R.Mark

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Increased biogenic amine release in mouse hypothalamus following immunological challenge: antagonism by indomethacin von Mefford, Ivan N., Heyes, Melvyn P.

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Neurotensin and cholecystokinin microinjected into the ventral tegmental area modulate microdialysate concentrations of dopamine and metabolites in the posterior nucleus accumbens von Laitinen, K., Crawley, J.N., Mefford, I.N., De Witte, Ph

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