DNM1 encephalopathy: A new disease of vesicle fission von von Spiczak, Sarah, Helbig, Katherine L, Shinde, Deepali N, Huether, Robert, Pendziwiat, Manuela, Lourenço, Charles, Nunes, Mark E, Sarco, Dean P, Kaplan, Richard A, Dlugos, Dennis J, Kirsch, Heidi, Slavotinek, Anne, Cilio, Maria R, Cervenka, Mackenzie C, Cohen, Julie S, McClellan, Rebecca, Fatemi, Ali, Yuen, Amy, Sagawa, Yoshimi, Littlejohn, Rebecca, McLean, Scott D, Hernandez-Hernandez, Laura, Maher, Bridget, Møller, Rikke S, Palmer, Elizabeth, Lawson, John A, Campbell, Colleen A, Joshi, Charuta N, Kolbe, Diana L, Hollingsworth, Georgie, Neubauer, Bernd A, Muhle, Hiltrud, Stephani, Ulrich, Scheffer, Ingrid E, Pena, Sérgio D.J, Sisodiya, Sanjay M, Helbig, Ingo

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Oxcarbazepine in Children With Nocturnal Frontal-Lobe Epilepsy von Raju, G. Praveen, MD, PhD, Sarco, Dean P., MD, Poduri, Annapurna, MD, Riviello, James J., MD, Bergin, Ann Marie R., MD, Takeoka, Masanori, MD

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The neuroprotective effect of deferoxamine in the hypoxic-ischemic immature mouse brain von Sarco, Dean P, Becker, Joseph, Palmer, Charles, Sheldon, R.Ann, Ferriero, Donna M

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Analysis of EEG patterns and genotypes in patients with Angelman syndrome von Vendrame, Martina, Loddenkemper, Tobias, Zarowski, Marcin, Gregas, Matt, Shuhaiber, Hans, Sarco, Dean P, Morales, Augusto, Nespeca, Mark, Sharpe, Cia, Haas, Kevin, Barnes, Gregory, Glaze, Daniel, Kothare, Sanjeev V

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Benign rolandic epileptiform discharges are associated with mood and behavior problems von Sarco, Dean P, Boyer, Katrina, Lundy-Krigbaum, Shannon M, Takeoka, Masanori, Jensen, Frances, Gregas, Matt, Waber, Deborah P

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The safety and tolerability of newer antiepileptic drugs in children and adolescents von Sarco, Dean P., Bourgeois, Blaise F. D.

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Septo‐Optic Dysplasia Complicated by Infantile Spasms and Bilateral Choroidal Fissure Arachnoid Cysts von Tas, Emir, Tracy, Molly, Sarco, Dean P., Eksioglu, Yaman Z., Prabhu, Sanjay P., Loddenkemper, Tobias

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Electroencephalography in epilepsy surgery planning von Sarco, Dean P, Burke, John F, Madsen, Joseph R

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Clinical genetic testing for patients with autism spectrum disorders von Shen, Yiping, Dies, Kira A, Holm, Ingrid A, Bridgemohan, Carolyn, Sobeih, Magdi M, Caronna, Elizabeth B, Miller, Karen J, Frazier, Jean A, Silverstein, Iris, Picker, Jonathan, Weissman, Laura, Raffalli, Peter, Jeste, Shafali, Demmer, Laurie A, Peters, Heather K, Brewster, Stephanie J, Kowalczyk, Sara J, Rosen-Sheidley, Beth, McGowan, Caroline, Duda, 3rd, Andrew W, Lincoln, Sharyn A, Lowe, Kathryn R, Schonwald, Alison, Robbins, Michael, Hisama, Fuki, Wolff, Robert, Becker, Ronald, Nasir, Ramzi, Urion, David K, Milunsky, Jeff M, Rappaport, Leonard, Gusella, James F, Walsh, Christopher A, Wu, Bai-Lin, Miller, David T

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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders von Ching, Michael S.L., Shen, Yiping, Tan, Wen-Hann, Jeste, Shafali S., Morrow, Eric M., Chen, Xiaoli, Mukaddes, Nahit M., Yoo, Seung-Yun, Hanson, Ellen, Hundley, Rachel, Austin, Christina, Becker, Ronald E., Berry, Gerard T., Driscoll, Katherine, Engle, Elizabeth C., Friedman, Sandra, Gusella, James F., Hisama, Fuki M., Irons, Mira B., Lafiosca, Tina, LeClair, Elaine, Miller, David T., Neessen, Michael, Picker, Jonathan D., Rappaport, Leonard, Rooney, Cynthia M., Sarco, Dean P., Stoler, Joan M., Walsh, Christopher A., Wolff, Robert R., Zhang, Ting, Nasir, Ramzi H., Wu, Bai-Lin

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Copper/zinc superoxide dismutase transgenic brain accumulates hydrogen peroxide after perinatal hypoxia ischemia von Fullerton, Heather J., Ditelberg, Jeremy S., Chen, Sylvia F., Sarco, Dean P., Chan, Pak H., Epstein, Charles J., Ferriero, Donna M.

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Septo-Optic Dysplasia Complicated by Infantile Spasms and Bilateral Choroidal Fissure Arachnoid Cysts von Tas, Emir, Tracy, Molly, Sarco, Dean P., Eksioglu, Yaman Z., Prabhu, Sanjay P., Loddenkemper, Tobias

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Angelman syndrome: Mutations influence features in early childhood von Tan, Wen-Hann, Bacino, Carlos A., Skinner, Steven A., Anselm, Irina, Barbieri-Welge, Rene, Bauer-Carlin, Astrid, Beaudet, Arthur L., Bichell, Terry Jo, Gentile, Jennifer K., Glaze, Daniel G., Horowitz, Lucia T., Kothare, Sanjeev V., Lee, Hye-Seung, Nespeca, Mark P., Peters, Sarika U., Sahoo, Trilochan, Sarco, Dean, Waisbren, Susan E., Bird, Lynne M.

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders von Valente, Enza Maria, Brancati, Francesco, Silhavy, Jennifer L., Castori, Marco, Marsh, Sarah E., Barrano, Giuseppe, Bertini, Enrico, Boltshauser, Eugen, Zaki, Maha S., Abdel-Aleem, Alice, Abdel-Salam, Ghada M. H., Bellacchio, Emanuele, Battini, Roberta, Cruse, Robert P., Dobyns, William B., Krishnamoorthy, Kalpathy S., Lagier-Tourenne, Clotilde, Magee, Alex, Pascual-Castroviejo, Ignacio, Salpietro, Carmelo D., Sarco, Dean, Dallapiccola, Bruno, Gleeson, Joseph G.

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A therapeutic trial of pro-methylation dietary supplements in Angelman syndrome von Bird, Lynne M., Tan, Wen-Hann, Bacino, Carlos A., Peters, Sarika U., Skinner, Steven A., Anselm, Irina, Barbieri-Welge, Rene, Bauer-Carlin, Astrid, Gentile, Jennifer K., Glaze, Daniel G., Horowitz, Lucia T., Mohan, K. Naga, Nespeca, Mark P., Sahoo, Trilochan, Sarco, Dean, Waisbren, Susan E., Beaudet, Arthur L.

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AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders von Valente, Enza Maria, Brancati, Francesco, Silhavy, Jennifer L, Castori, Marco, Marsh, Sarah E, Barrano, Giuseppe, Bertini, Enrico, Boltshauser, Eugen, Zaki, Maha S, Abdel-Aleem, Alice, Abdel-Salam, Ghada MH, Bellacchio, Emanuele, Battini, Roberta, Cruse, Robert P, Dobyns, William B, Krishnamoorthy, Kalpathy S, Lagier-Tourenne, Clotilde, Magee, Alex, Pascual-Castroviejo, Ignacio, Salpietro, Carmelo D, Sarco, Dean, Dallapiccola, Bruno, Gleeson, Joseph G

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