Search Results - Nespeca, Mark

Photosensitive Epilepsy Syndromes Mimicking Motor Tics by Longardner, Katherine, Desai, Soaham, Nespeca, Mark, Bainbridge, Matthew, Friedman, Jennifer

Get full text Get full text Get full text

Clinical characterization of epilepsy in children with Angelman syndrome by Cassater, Daiana, Bustamante, Mariana, Sach-Peltason, Lisa, Rotenberg, Alexander, Nespeca, Mark, Tan, Wen-Hann, Bird, Lynne M., Hipp, Joerg F.

Get full text Get full text Get full text

Practice guideline update summary: Efficacy and tolerability of the new antiepileptic drugs I: Treatment of new-onset epilepsy: Report of the American Epilepsy Society and the Guid... by Kanner, Andres M., Ashman, Eric, Gloss, David, Harden, Cynthia, Bourgeois, Blaise, Bautista, Jocelyn F., Abou-Khalil, Bassel, Burakgazi-Dalkilic, Evren, Park, Esmeralda Llanas, Stern, John, Hirtz, Deborah, Nespeca, Mark, Gidal, Barry, Faught, Edward, French, Jacqueline

Get full text Get full text Get full text

Practice guideline update summary: Efficacy and tolerability of the new antiepileptic drugs II: Treatment-resistant epilepsy: Report of the American Epilepsy Society and the Guidel... by Kanner, Andres M., Ashman, Eric, Gloss, David, Harden, Cynthia, Bourgeois, Blaise, Bautista, Jocelyn F., Abou-Khalil, Bassel, Burakgazi-Dalkilic, Evren, Park, Esmeralda Llanas, Stern, John, Hirtz, Deborah, Nespeca, Mark, Gidal, Barry, Faught, Edward, French, Jacqueline

Get full text Get full text Get full text

Double-Blind Therapeutic Trial in Angelman Syndrome Using Betaine and Folic Acid by Peters, Sarika U., Bird, Lynne M., Kimonis, Virginia, Glaze, Daniel G., Shinawi, Lina M., Bichell, Terry Jo, Barbieri-Welge, Rene, Nespeca, Mark, Anselm, Irina, Waisbren, Susan, Sanborn, Erica, Sun, Qin, O’Brien, William E., Beaudet, Arthur L., Bacino, Carlos A.

Get full text Get full text Get full text

A Therapeutic Trial of Pro-methylation Dietary Supplements in Angelman Syndrome by 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.

Get full text Get full text Get full text

Angelman Syndrome: Mutations Influence Features in Early Childhood by 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.

Get full text Get full text Get full text

Levetiracetam Versus Phenobarbital for Neonatal Seizures: A Randomized Controlled Trial by Sharpe, Cynthia, Reiner, Gail E., Davis, Suzanne L., Nespeca, Mark, Gold, Jeffrey J., Rasmussen, Maynard, Kuperman, Rachel, Harbert, Mary Jo, Michelson, David, Joe, Priscilla, Wang, Sonya, Rismanchi, Neggy, Le, Ngoc Minh, Mower, Andrew, Kim, Jae, Battin, Malcolm R., Lane, Brian, Honold, Jose, Knodel, Ellen, Arnell, Kathy, Bridge, Renee, Lee, Lilly, Ernstrom, Karin, Raman, Rema, Haas, Richard H.

Get full text Get full text Get full text

A Randomized Controlled Trial of Levodopa in Patients with Angelman Syndrome by Tan, Wen-Hann, Bird, Lynne M., Sadhwani, Anjali, Barbieri-Welge, Rene L., Skinner, Steven A., Horowitz, Lucia T., Bacino, Carlos A., Noll, Lisa M., Fu, Cary, Hundley, Rachel J., Wink, Logan K., Erickson, Craig A., Barnes, Gregory N., Slavotinek, Anne, Jeremy, Rita, Rotenberg, Alexander, Kothare, Sanjeev V., Olson, Heather E., Poduri, Annapurna, Nespeca, Mark P., Chu, Hillary C., Willen, Jennifer M., Haas, Kevin F., Weeber, Edwin J., Rufo, Paul A.

Get full text Get full text Get full text

Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions by Lee, Hsien-Yang, Huang, Yong, Bruneau, Nadine, Roll, Patrice, Roberson, Elisha D.O., Hermann, Mark, Quinn, Emily, Maas, James, Edwards, Robert, Ashizawa, Tetsuo, Baykan, Betul, Bhatia, Kailash, Bressman, Susan, Bruno, Michiko K., Brunt, Ewout R., Caraballo, Roberto, Echenne, Bernard, Fejerman, Natalio, Frucht, Steve, Gurnett, Christina A., Hirsch, Edouard, Houlden, Henry, Jankovic, Joseph, Lee, Wei-Ling, Lynch, David R., Mohamed, Shehla, Müller, Ulrich, Nespeca, Mark P., Renner, David, Rochette, Jacques, Rudolf, Gabrielle, Saiki, Shinji, Soong, Bing-Wen, Swoboda, Kathryn J., Tucker, Sam, Wood, Nicholas, Hanna, Michael, Bowcock, Anne, Szepetowski, Pierre, Fu, Ying-Hui, Ptáček, Louis J.

Get full text Get full text Get full text

A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome by Duis, Jessica, Nespeca, Mark, Summers, Jane, Bird, Lynne, Bindels‐de Heus, Karen G.C.B., Valstar, M. J., de Wit, Marie‐Claire Y., Navis, C., ten Hooven‐Radstaake, Maartje, van Iperen‐Kolk, Bianca M., Ernst, Susan, Dendrinos, Melina, Katz, Terry, Diaz‐Medina, Gloria, Katyayan, Akshat, Nangia, Srishti, Thibert, Ronald, Glaze, Daniel, Keary, Christopher, Pelc, Karine, Simon, Nicole, Sadhwani, Anjali, Heussler, Helen, Wheeler, Anne, Woeber, Caroline, DeRamus, Margaret, Thomas, Amy, Kertcher, Emily, DeValk, Lauren, Kalemeris, Kristen, Arps, Kara, Baym, Carol, Harris, Nicole, Gorham, John P., Bohnsack, Brenda L., Chambers, Reid C., Harris, Sarah, Chambers, Henry G., Okoniewski, Katherine, Jalazo, Elizabeth R., Berent, Allyson, Bacino, Carlos A., Williams, Charles, Anderson, Anne

Get full text Get full text Get full text

Defining the phenotypic spectrum of SLC6A1 mutations by Johannesen, Katrine M., Gardella, Elena, Linnankivi, Tarja, Courage, Carolina, de Saint Martin, Anne, Lehesjoki, Anna-Elina, Mignot, Cyril, Afenjar, Alexandra, Lesca, Gaetan, Abi-Warde, Marie-Thérèse, Chelly, Jamel, Piton|, Amélie, Merritt, J. Lawrence, Rodan, Lance H., Tan, Wen-Hann, Bird, Lynne M., Nespeca, Mark, Gleeson, Joseph G., Yoo, Yongjin, Choi, Murim, Chae, Jong-Hee, Czapansky-Beilman, Desiree, Reichert, Sara Chadwick, Pendziwiat, Manuela, Verhoeven, Judith S., Schelhaas, Helenius J., Devinsky, Orrin, Christensen, Jakob, Specchio, Nicola, Trivisano, Marina, Weber, Yvonne G., Nava, Caroline, Keren, Boris, Doummar, Diane, Schaefer, Elise, Hopkins, Sarah, Dubbs, Holly, Shaw, Jessica E., Pisani, Laura, Myers, Candace T., Tang, Sha, Tang, Shan, Pal, Deb K., Millichap, John J., Carvill, Gemma L., Helbig, Kathrine L., Mecarelli, Oriano, Striano, Pasquale, Helbig, Ingo, Rubboli, Guido, Mefford, Heather C., Møller, Rikke S.

Get full text Get full text Get full text

An automated 13.5 hour system for scalable diagnosis and acute management guidance for genetic diseases by Owen, Mallory J., Lefebvre, Sebastien, Hansen, Christian, Kunard, Chris M., Dimmock, David P., Smith, Laurie D., Scharer, Gunter, Mardach, Rebecca, Willis, Mary J., Feigenbaum, Annette, Niemi, Anna-Kaisa, Ding, Yan, Van Der Kraan, Luca, Ellsworth, Katarzyna, Guidugli, Lucia, Lajoie, Bryan R., McPhail, Timothy K., Mehtalia, Shyamal S., Chau, Kevin K., Kwon, Yong H., Zhu, Zhanyang, Batalov, Sergey, Chowdhury, Shimul, Rego, Seema, Perry, James, Speziale, Mark, Nespeca, Mark, Wright, Meredith S., Reese, Martin G., De La Vega, Francisco M., Azure, Joe, Frise, Erwin, Rigby, Charlene Son, White, Sandy, Hobbs, Charlotte A., Gilmer, Sheldon, Knight, Gail, Oriol, Albert, Lenberg, Jerica, Nahas, Shareef A., Perofsky, Kate, Kim, Kyu, Carroll, Jeanne, Coufal, Nicole G., Sanford, Erica, Wigby, Kristen, Weir, Jacqueline, Thomson, Vicki S., Fraser, Louise, Lazare, Seka S., Shin, Yoon H., Grunenwald, Haiying, Lee, Richard, Jones, David, Tran, Duke, Gross, Andrew, Daigle, Patrick, Case, Anne, Lue, Marisa, Richardson, James A., Reynders, John, Defay, Thomas, Hall, Kevin P., Veeraraghavan, Narayanan, Kingsmore, Stephen F.

Get full text Get full text Get full text