Stiripentol in Dravet syndrome: Results of a retrospective U.S. study von Wirrell, Elaine C., Laux, Linda, Franz, David N., Sullivan, Joseph, Saneto, Russell P., Morse, Richard P., Devinsky, Orrin, Chugani, Harry, Hernandez, Angel, Hamiwka, Lorie, Mikati, Mohamad A., Valencia, Ignacio, Le Guern, Marie‐Emmanuelle, Chancharme, Laurent, Menezes, Marcio Sotero

Volltext

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry von Viollet, Louis, Glusman, Gustavo, Murphy, Kelley J, Newcomb, Tara M, Reyna, Sandra P, Sweney, Matthew, Nelson, Benjamin, Andermann, Frederick, Andermann, Eva, Acsadi, Gyula, Barbano, Richard L, Brown, Candida, Brunkow, Mary E, Chugani, Harry T, Cheyette, Sarah R, Collins, Abigail, DeBrosse, Suzanne D, Galas, David, Friedman, Jennifer, Hood, Lee, Huff, Chad, Jorde, Lynn B, King, Mary D, LaSalle, Bernie, Leventer, Richard J, Lewelt, Aga J, Massart, Mylynda B, Mérida, 2nd, Mario R, Ptáček, Louis J, Roach, Jared C, Rust, Robert S, Renault, Francis, Sanger, Terry D, Sotero de Menezes, Marcio A, Tennyson, Rachel, Uldall, Peter, Zhang, Yue, Zupanc, Mary, Xin, Winnie, Silver, Kenneth, Swoboda, Kathryn J

Volltext

Disruption of cellular iron homeostasis by IREB2 missense variants causes severe neurodevelopmental delay, dystonia and seizures von Maio, Nunziata, Saneto, Russell P., Steet, Richard, Sotero de Menezes, Marcio A., Skinner, Cindy, Rouault, Tracey A.

Volltext

Clinical and Electrographic Features of Epileptic Spasms Persisting Beyond the Second Year of Life von De Menezes, Márcio A. Sotero, Rho, Jong M.

Volltext

Cerebral MRI abnormalities associated with vigabatrin therapy von Pearl, Phillip L., Vezina, Louis G., Saneto, Russell P., McCarter, Robert, Molloy‐Wells, Elizabeth, Heffron, Ari, Trzcinski, Stacey, McClintock, William M., Conry, Joan A., Elling, Nancy J., Goodkin, Howard P., De Menezes, Marcio Sotero, Ferri, Raymond, Gilles, Elizabeth, Kadom, Nadja, Gaillard, William D.

Volltext

Research conference summary from the 2014 International Task Force on ATP1A3 -Related Disorders von Rosewich, Hendrik, Sweney, Matthew T, DeBrosse, Suzanne, Ess, Kevin, Ozelius, Laurie, Andermann, Eva, Andermann, Frederick, Andrasco, Gene, Belgrade, Alice, Brashear, Allison, Ciccodicola, Sharon, Egan, Lynn, George, Jr, Alfred L, Lewelt, Aga, Magelby, Joshua, Merida, Mario, Newcomb, Tara, Platt, Vicky, Poncelin, Dominic, Reyna, Sandra, Sasaki, Masayuki, Sotero de Menezes, Marcio, Sweadner, Kathleen, Viollet, Louis, Zupanc, Mary, Silver, Kenneth, Swoboda, Kathryn

Volltext

Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry von Viollet, Louis, Glusman, Gustavo, Murphy, Kelley J, Newcomb, Tara M, Reyna, Sandra P, Sweney, Matthew, Nelson, Benjamin, Andermann, Frederick, Andermann, Eva, Acsadi, Gyula, Barbano, Richard L, Brown, Candida, Brunkow, Mary E, Chugani, Harry T, Cheyette, Sarah R, Collins, Abigail, DeBrosse, Suzanne D, Galas, David, Friedman, Jennifer, Hood, Lee, Huff, Chad, Jorde, Lynn B, King, Mary D, LaSalle, Bernie, Leventer, Richard J, Lewelt, Aga J, Massart, Mylynda B, Mérida, 2nd, Mario R, Ptáček, Louis J, Roach, Jared C, Rust, Robert S, Renault, Francis, Sanger, Terry D, Sotero de Menezes, Marcio A, Tennyson, Rachel, Uldall, Peter, Zhang, Yue, Zupanc, Mary, Xin, Winnie, Silver, Kenneth, Swoboda, Kathryn J

Volltext

Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial von Lagae, Lieven, Sullivan, Joseph, Knupp, Kelly, Laux, Linda, Polster, Tilman, Nikanorova, Marina, Devinsky, Orrin, Cross, J Helen, Guerrini, Renzo, Talwar, Dinesh, Miller, Ian, Farfel, Gail, Galer, Bradley S, Gammaitoni, Arnold, Mistry, Arun, Morrison, Glenn, Lock, Michael, Agarwal, Anupam, Lai, Wyman W, Ceulemans, Berten

Volltext

The semiology of benign focal epilepsy with affective symptoms von Nascimento, Fábio A., Sotero de Menezes, Márcio A., Simão, Cristiane A., Takeshita, Bruno T., Blattes da Rocha, Samanta F., Kowacs, Pedro A.

Volltext

Persistence of Suppression-Bursts in a Patient With Ohtahara Syndrome von Saneto, Russell P., Sotero de Menezes, Marcio

Volltext

Vagus Nerve Stimulation for Intractable Seizures in Children von Saneto, Russell P., Sotero de Menezes, Marcio A., Ojemann, Jeffrey G., Bournival, Brian D., Murphy, Patricia J., Cook, William B., Avellino, Anthony M., Ellenbogen, Richard G.

Volltext

Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects von Craig, Alexa K, de Menezes, Marcio Sotero, Saneto, Russell P

Volltext

Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial von Lagae, Lieven, Sullivan, Joseph, Knupp, Kelly, Laux, Linda, Polster, Tilman, Nikanorova, Marina, Devinsky, Orrin, Cross, J. Helen, Guerrini, Renzo, Talwar, Dinesh, Miller, Ian, Farfel, Gail, Galer, Bradley S, Gammaitoni, Arnold, Mistry, Arun, Morrison, Glenn, Lock, Michael, Agarwal, Anupam, Lai, Wyman W, Ceulemans, Berten, Gill, Deepak, Riney, Kate, Scheffer, Ingrid, Buchhalter, Jeffrey, Carmant, Lionel, Connolly, Mary, Nabbout, Rima, Brandt, Ulrich, Jacobs-LeVan, Julia, Mayer, Thomas, Panzer, Axel, Pringsheim, Milka, Stephani, Ulrich, Wolff, Markus, Battaglia, Domenica, Beccaria, Francesca, Dana, Francesca, Granata, Tiziana, Romeo, Antonio, Striano, Pasquale, Vigevano, Federico, Gil-Nagel, Antonio, San Antonio, Victoria, Sanchez-Carpintero, Rocio, Desurkar, Archana, Hughes, Elaine, Lyer, Anand, Philip, Sunny, Zuberi, Sameer, Sharp, Gregory, Berenson, Frank, Faux, Linda, Marsh, Eric, Nespeca, Mark, Nahouraii, Robert, Paolicdii, Juliann, Phillips, Steven, Perry, Michael Scott, Poduri, Annapurna, Renfroe, Ben, Saneto, Russell, Shahid, Asim, Smith, Douglas, de Menezes, Marcio Sotero, Sweney, Matthew, Thiele, Elizabeth, Wheless, James, Wilfong, Angus, Wirrell, Elaine, Zupanc, Mary

Volltext

Lamotrigine‐Induced Tic Disorder: Report of Five Pediatric Cases von Menezes, Márcio Affonseca Sotero, Rho, Jong M., Murphy, Patti, Cheyette, Sarah

Volltext

Moyamoya Syndrome in a Patient With Congenital Human Immunodeficiency Virus Infection von Hsiung, Ging-Yuek R., Marcio Sotero de Menezes

Volltext

Stiripentol in D ravet syndrome: Results of a retrospective U . S . study von Wirrell, Elaine C., Laux, Linda, Franz, David N., Sullivan, Joseph, Saneto, Russell P., Morse, Richard P., Devinsky, Orrin, Chugani, Harry, Hernandez, Angel, Hamiwka, Lorie, Mikati, Mohamad A., Valencia, Ignacio, Le Guern, Marie‐Emmanuelle, Chancharme, Laurent, de Menezes, Marcio Sotero

Volltext

Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects von Craig⁎, Alexa K., de Menzes, Marcio Sotero, Saneto, Russell P.

Volltext

Walker-Warburg syndrome. Report of two cases von Vasconcelos, M M, Guedes, C R, Domingues, R C, Vianna, R N, Sotero, M, Vieira, M M

Volltext

Pediatric Tramadol Ingestion Resulting in Seizurelike Activity: A Case Series von Mazor, Suzan S, Feldman, Kenneth W, Sugar, Naomi F, Sotero, Marcio

Volltext

Pretreatment behavior and subsequent medication effects in childhood absence epilepsy von Shinnar, Ruth C, Shinnar, Shlomo, Cnaan, Avital, Clark, Peggy, Dlugos, Dennis, Hirtz, Deborah G, Hu, Fengming, Liu, Chunyan, Masur, David, Weiss, Erica F, Glauser, Tracy A

Volltext