Visual hallucinations: A novel complication after hemispherectomy

por Vanags, Jonas, Sachdev, Monisha, Grant, Gerald, Mikati, Mohamad A.
Publicado 2017

Neuronal mechanism of a BK channelopathy in absence epilepsy and dyskinesia

por Dong, Ping, Zhang, Yang, Hunanyan, Arsen S., Mikati, Mohamad A., Cui, Jianmin, Yang, Huanghe
Publicado 2022

Paroxysmal Genetic Movement Disorders and Epilepsy

por de Gusmão, Claudio M., Garcia, Lucas, Mikati, Mohamad A., Su, Samantha, Silveira-Moriyama, Laura
Publicado 2021

Brain structural connectivity increases concurrent with functional improvement: Evidence from diffusion tensor MRI in children with cerebral palsy during therapy

por Englander, Zoë A., Sun, Jessica, Laura Case, Mikati, Mohamad A., Kurtzberg, Joanne, Song, Allen W.
Publicado 2015

Diffuse reduction of white matter connectivity in cerebral palsy with specific vulnerability of long range fiber tracts()

por Englander, Zoë A., Pizoli, Carolyn E., Batrachenko, Anastasiya, Sun, Jessica, Worley, Gordon, Mikati, Mohamad A., Kurtzberg, Joanne, Song, Allen W.
Publicado 2013

Reorganization and Stability for Motor and Language Areas Using Cortical Stimulation: Case Example and Review of the Literature

por Serafini, Sandra, Komisarow, Jordan M., Gallentine, William, Mikati, Mohamad A., Bonner, Melanie J., Kranz, Peter G., Haglund, Michael M., Grant, Gerald
Publicado 2013

Sibling umbilical cord blood infusion is safe in young children with cerebral palsy

por Sun, Jessica M., Case, Laura E., Mikati, Mohamad A., M. Jasien, Joan, McLaughlin, Colleen, Waters‐Pick, Barbara, Worley, Gordon, Troy, Jesse, Kurtzberg, Joanne
Publicado 2021

Motor function and safety after allogeneic cord blood and cord tissue‐derived mesenchymal stromal cells in cerebral palsy: An open‐label, randomized trial

por Sun, Jessica M., Case, Laura E., McLaughlin, Colleen, Burgess, Alicia, Skergan, Natalie, Crane, Sydney, Jasien, Joan M., Mikati, Mohamad A., Troy, Jesse, Kurtzberg, Joanne
Publicado 2022

Sustained therapeutic response to riboflavin in a child with a progressive neurological condition, diagnosed by whole-exome sequencing

por Shashi, Vandana, Petrovski, Slavé, Schoch, Kelly, Crimian, Rebecca, Case, Laura E., Khalid, Roha, El-Dairi, Maysantoine A., Jiang, Yong-Hui, Mikati, Mohamad A., Goldstein, David B.
Publicado 2015

Alternating Hemiplegia of Childhood: gastrointestinal manifestations and correlation with neurological impairments

por Pratt, Milton, Uchitel, Julie, McGreal, Nancy, Gordon, Kelly, Prange, Lyndsey, McLean, Melissa, Noel, Richard J., Rikard, Blaire, Rogers Boruta, Mary K., Mikati, Mohamad A.
Publicado 2020

Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly

por Griffin, Nicole G., Cronin, Kenneth D., Walley, Nicole M., Hulette, Christine M., Grant, Gerald A., Mikati, Mohamad A., LaBreche, Heather G., Rehder, Catherine W., Allen, Andrew S., Crino, Peter B., Heinzen, Erin L.
Publicado 2017

D-DEMØ, a distinct phenotype caused by ATP1A3 mutations

por Prange, Lyndsey, Pratt, Milton, Herman, Kristin, Schiffmann, Raphael, Mueller, David M., McLean, Melissa, Mendez, Mary Moya, Walley, Nicole, Heinzen, Erin L., Goldstein, David, Shashi, Vandana, Hunanyan, Arsen, Pagadala, Vijay, Mikati, Mohamad A.
Publicado 2020

Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition

por Petrovski, Slavé, Shashi, Vandana, Petrou, Steven, Schoch, Kelly, McSweeney, Keisha Melodi, Dhindsa, Ryan S., Krueger, Brian, Crimian, Rebecca, Case, Laura E., Khalid, Roha, El-Dairi, Maysantoine A., Jiang, Yong-Hui, Mikati, Mohamad A., Goldstein, David B.
Publicado 2015

Effect of Autologous Cord Blood Infusion on Motor Function and Brain Connectivity in Young Children with Cerebral Palsy: A Randomized, Placebo‐Controlled Trial

por Sun, Jessica M., Song, Allen W., Case, Laura E., Mikati, Mohamad A., Gustafson, Kathryn E., Simmons, Ryan, Goldstein, Ricki, Petry, Jodi, McLaughlin, Colleen, Waters‐Pick, Barbara, Chen, Lyon W., Wease, Stephen, Blackwell, Beth, Worley, Gordon, Troy, Jesse, Kurtzberg, Joanne
Publicado 2017

Phenotype and mutation expansion of the PTPN23 associated disorder characterized by neurodevelopmental delay and structural brain abnormalities

por Bend, Renee, Cohen, Lior, Carter, Melissa T., Lyons, Michael J., Niyazov, Dmitriy, Mikati, Mohamad A., Rojas, Samantha K., Person, Richard E., Si, Yue, Wentzensen, Ingrid M., Torti, Erin, Lee, Jennifer A., Boycott, Kym M., Basel-Salmon, Lina, Ferreira, Carlos R., Gonzaga-Jauregui, Claudia
Publicado 2019

Alternating hemiplegia of childhood: evolution over time and mouse model corroboration

por Uchitel, Julie, Wallace, Keri, Tran, Linh, Abrahamsen, Tavis, Hunanyan, Arsen, Prange, Lyndsey, Jasien, Joan, Caligiuri, Laura, Pratt, Milton, Rikard, Blaire, Fons, Carmen, De Grandis, Elisa, Vezyroglou, Aikaterini, Heinzen, Erin L, Goldstein, David B, Vavassori, Rosaria, Papadopoulou, Maria T, Cocco, Isabella, Moré, Rebecca, Arzimanoglou, Alexis, Panagiotakaki, Eleni, Mikati, Mohamad A
Publicado 2021

ATP1A3‐Encoded Sodium‐Potassium ATPase Subunit Alpha 3 D801N Variant Is Associated With Shortened QT Interval and Predisposition to Ventricular Fibrillation Preceded by Bradycardia...

por Moya‐Mendez, Mary E., Ogbonna, Chiagoziem, Ezekian, Jordan E., Rosamilia, Michael B., Prange, Lyndsey, de la Uz, Caridad, Kim, Jeffrey J., Howard, Taylor, Garcia, John, Nussbaum, Robert, Truty, Rebecca, Callis, Thomas E., Funk, Emily, Heyes, Matthew, Dear, Guy de Lisle, Carboni, Michael P., Idriss, Salim F., Mikati, Mohamad A., Landstrom, Andrew P.
Publicado 2021

Gaps and opportunities in refractory status epilepticus research in children: A multi-center approach by the Pediatric Status Epilepticus Research Group (pSERG)

por Fernández, Iván Sánchez, Abend, Nicholas S., Agadi, Satish, An, Sookee, Arya, Ravindra, Carpenter, Jessica L., Chapman, Kevin E., Gaillard, William D., Glauser, Tracy A., Goldstein, David B., Goldstein, Joshua L., Goodkin, Howard P., Hahn, Cecil D., Heinzen, Erin L., Mikati, Mohamad A., Peariso, Katrina, Pestian, John P., Ream, Margie, Riviello, James J., Tasker, Robert C., Williams, Korwyn, Loddenkemper, Tobias
Publicado 2013

Clinical presentation of new onset refractory status epilepticus in children (the pSERG cohort)

por Sculier, Claudine, Barcia Aguilar, Cristina, Gaspard, Nicolas, Gaínza‐Lein, Marina, Sánchez Fernández, Iván, Amengual‐Gual, Marta, Anderson, Anne, Arya, Ravindra, Burrows, Brian T., Brenton, James N., Carpenter, Jessica L., Chapman, Kevin E., Clark, Justice, Gaillard, William D., Glauser, Tracy A., Goldstein, Joshua L., Goodkin, Howard P., Gorman, Mark, Lai, Yi‐Chen, McDonough, Tiffani L., Mikati, Mohamad A., Nayak, Anuranjita, Peariso, Katrina, Riviello, James, Rusie, Allison, Sperberg, Katherine, Stredny, Coral M., Tasker, Robert C., Tchapyjnikov, Dmitry, Vasquez, Alejandra, Wainwright, Mark S., Wilfong, Angus A., Williams, Korwyn, Loddenkemper, Tobias
Publicado 2021

Association of guideline publication and delays to treatment in pediatric status epilepticus

por Sánchez Fernández, Iván, Abend, Nicholas S., Amengual-Gual, Marta, Anderson, Anne, Arya, Ravindra, Barcia Aguilar, Cristina, Brenton, James Nicholas, Carpenter, Jessica L., Chapman, Kevin E., Clark, Justice, Farias-Moeller, Raquel, Gaillard, William D., Gaínza-Lein, Marina, Glauser, Tracy, Goldstein, Joshua, Goodkin, Howard P., Guerriero, Réjean M., Lai, Yi-Chen, McDonough, Tiffani, Mikati, Mohamad A., Morgan, Lindsey A., Novotny, Edward, Payne, Eric, Peariso, Katrina, Piantino, Juan, Ostendorf, Adam, Sands, Tristan T., Sannagowdara, Kumar, Tasker, Robert C., Tchapyjnikov, Dimtry, Topjian, Alexis A., Vasquez, Alejandra, Wainwright, Mark S., Wilfong, Angus, Williams, Kowryn, Loddenkemper, Tobias
Publicado 2020