Search Results - Mikati, Mohamad A.

Visual hallucinations: A novel complication after hemispherectomy by Vanags, Jonas, Sachdev, Monisha, Grant, Gerald, Mikati, Mohamad A.

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Neuronal mechanism of a BK channelopathy in absence epilepsy and dyskinesia by Dong, Ping, Zhang, Yang, Hunanyan, Arsen S., Mikati, Mohamad A., Cui, Jianmin, Yang, Huanghe

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Cognitive and motor function in adults with spina bifida myelomeningocele: a pilot study by Jasien, Joan Mary, Mikati, Mohamad A., Kolarova, Michaela, Smith, Brian, Thera, Stephanie, Lee, Pierre

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Paroxysmal Genetic Movement Disorders and Epilepsy by de Gusmão, Claudio M., Garcia, Lucas, Mikati, Mohamad A., Su, Samantha, Silveira-Moriyama, Laura

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Brain structural connectivity increases concurrent with functional improvement: Evidence from diffusion tensor MRI in children with cerebral palsy during therapy by Englander, Zoë A., Sun, Jessica, Laura Case, Mikati, Mohamad A., Kurtzberg, Joanne, Song, Allen W.

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Polysomnography Findings and Sleep Disorders in Children With Alternating Hemiplegia of Childhood by Kansagra, Sujay, Ghusayni, Ryan, Kherallah, Bassil, Gunduz, Talha, McLean, Melissa, Prange, Lyndsey, Kravitz, Richard M., Mikati, Mohamad A.

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Diffuse reduction of white matter connectivity in cerebral palsy with specific vulnerability of long range fiber tracts() by Englander, Zoë A., Pizoli, Carolyn E., Batrachenko, Anastasiya, Sun, Jessica, Worley, Gordon, Mikati, Mohamad A., Kurtzberg, Joanne, Song, Allen W.

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Reorganization and Stability for Motor and Language Areas Using Cortical Stimulation: Case Example and Review of the Literature by Serafini, Sandra, Komisarow, Jordan M., Gallentine, William, Mikati, Mohamad A., Bonner, Melanie J., Kranz, Peter G., Haglund, Michael M., Grant, Gerald

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A Gain-of-Function Mutation in KCNMA1 Causes Dystonia Spells Controlled with Stimulant Therapy by Zhang, Guohui, Gibson, Rebecca A., McDonald, Marie, Liang, Pengfei, Kang, Po Wei, Shi, Jingyi, Yang, Huanghe, Cui, Jianmin, Mikati, Mohamad A.

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Sibling umbilical cord blood infusion is safe in young children with cerebral palsy by Sun, Jessica M., Case, Laura E., Mikati, Mohamad A., M. Jasien, Joan, McLaughlin, Colleen, Waters‐Pick, Barbara, Worley, Gordon, Troy, Jesse, Kurtzberg, Joanne

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

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Alternating Hemiplegia of Childhood: gastrointestinal manifestations and correlation with neurological impairments by Pratt, Milton, Uchitel, Julie, McGreal, Nancy, Gordon, Kelly, Prange, Lyndsey, McLean, Melissa, Noel, Richard J., Rikard, Blaire, Rogers Boruta, Mary K., Mikati, Mohamad A.

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Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant by Millichap, John J., Miceli, Francesco, De Maria, Michela, Keator, Cynthia, Joshi, Nishtha, Tran, Baouyen, Soldovieri, Maria Virginia, Ambrosino, Paolo, Shashi, Vandana, Mikati, Mohamad A., Cooper, Edward C., Taglialatela, Maurizio

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Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy by Holt, Rebecca L., Provenzale, James M., Veerapandiyan, Aravindhan, Moon, Won-Jin, De Bellis, Michael D., Leonard, Soren, Gallentine, William B., Grant, Gerald A., Egger, Helen, Song, Allen W., Mikati, Mohamad A.

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Somatic uniparental disomy of Chromosome 16p in hemimegalencephaly by 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.

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D-DEMØ, a distinct phenotype caused by ATP1A3 mutations by 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.

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Early Onset Severe ATP1A2 Epileptic Encephalopathy: Clinical Characteristics and Underlying Mutations by Moya-Mendez, Mary E., Mueller, David M., Pratt, Milton, Bonner, Melanie, Elliott, Courtney, Hunanyan, Arsen, Kucera, Gary, Bock, Cheryl, Prange, Lyndsey, Jasien, Joan, Keough, Karen, Shashi, Vandana, McDonald, Marie, Mikati, Mohamad A.

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Adeno-Associated Virus-Mediated Gene Therapy in the Mashlool, Atp1a3(Mashl/+), Mouse Model of Alternating Hemiplegia of Childhood by Hunanyan, Arsen S., Kantor, Boris, Puranam, Ram S., Elliott, Courtney, McCall, Angela, Dhindsa, Justin, Pagadala, Promila, Wallace, Keri, Poe, Jordan, Gunduz, Talha, Asokan, Aravind, Koeberl, Dwight D., ElMallah, Mai K., Mikati, Mohamad A.

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Quinidine in the Treatment of KCNT1-Positive Epilepsies by Mikati, Mohamad A, Jiang, Yong-hui, Carboni, Michael, Shashi, Vandana, Petrovski, Slave, Spillmann, Rebecca, Milligan, Carol J., Li, Melody, Grefe, Annette, McConkie, Allyn, Berkovic, Samuel, Scheffer, Ingrid, Mullen, Saul, Bonner, Melanie, Petrou, Steven, Goldstein, David

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

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