Enhancing early child development a handbook for clinicians /

Por Sinno, Durriyah., Charafeddine, Lama., Mikati, Mohamad.
Publicado em 2013

Importance of voltage-dependent inactivation in N-type calcium channel regulation by G-proteins

Por Weiss, Norbert, Tadmouri, Abir, Mikati, Mohamad, Ronjat, Michel, De Waard, Michel
Publicado em 2007

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 no Neuroimage Clin (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 em 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 em 2013

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 no Cold Spring Harb Mol Case Stud (2015)

Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain-of-function variant

Por 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
Publicado no Epilepsia (2016)

Structural connectivity of the frontal lobe in children with drug-resistant partial epilepsy

Por 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.
Publicado em 2011

Quinidine in the Treatment of KCNT1-Positive Epilepsies

Por 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
Publicado no Ann Neurol (2015)

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 no Cold Spring Harb Mol Case Stud (2015)

Distinct neurological disorders with ATP1A3 mutations

Por Heinzen, Erin L., Arzimanoglou, Alexis, Brashear, Allison, Clapcote, Steven J., Gurrieri, Fiorella, Goldstein, David B., Jóhannesson, Sigurður H., Mikati, Mohamad A., Neville, Brian, Nicole, Sophie, Ozelius, Laurie J., Poulsen, Hanne, Schyns, Tsveta, Sweadner, Kathleen J., van den Maagdenberg, Arn, Vilsen, Bente
Publicado no Lancet Neurol (2014)

Time from convulsive status epilepticus onset to anticonvulsant administration in children

Por Sánchez Fernández, Iván, Abend, Nicholas S., Agadi, Satish, An, Sookee, Arya, Ravindra, Brenton, James Nicholas, Carpenter, Jessica L., Chapman, Kevin E., Gaillard, William D., Glauser, Tracy A., Goodkin, Howard P., Kapur, Kush, Mikati, Mohamad A., Peariso, Katrina, Ream, Margie, Riviello, James, Tasker, Robert C., Loddenkemper, Tobias
Publicado no Neurology (2015)

Neonatal Non-Epileptic Myoclonus is a Prominent Clinical Feature of KCNQ2 Gain-of-Function Variants R201C and R201H

Por Mulkey, Sarah B., Ben-Zeev, Bruria, Nicolai, Joost, Carroll, John L., Grønborg, Sabine, Jiang, Yong-hui, Joshi, Nishtha, Kelly, Megan, Koolen, David. A., Mikati, Mohamad A., Park, Kristen, Pearl, Phillip L., Scheffer, Ingrid E., Spillmann, Rebecca C., Taglialatela, Maurizio, Vieker, Silvia, Weckhuysen, Sarah, Cooper, Edward C., Cilio, Maria Roberta
Publicado no Epilepsia (2017)

Refractory Status Epilepticus in Children: intention-to-treat with continuous infusions of midazolam and pentobarbital

Por Tasker, Robert C, Goodkin, Howard P, Fernández, Iván Sánchez, Chapman, Kevin E, Abend, Nicholas S, Arya, Ravindra, Brenton, James N, Carpenter, Jessica L, Gaillard, William D, Glauser, Tracy A, Goldstein, Joshua, Helseth, Ashley R, Jackson, Michele C, Kapur, Kush, Mikati, Mohamad A, Peariso, Katrina, Wainwright, Mark S, Wilfong, Angus A, Williams, Korwyn, Loddenkemper, Tobias
Publicado no Pediatr Crit Care Med (2016)

Refractory status epilepticus in children with and without prior epilepsy or status epilepticus

Por Sánchez Fernández, Iván, Jackson, Michele C., Abend, Nicholas S., Arya, Ravindra, Brenton, James N., Carpenter, Jessica L., Chapman, Kevin E., Gaillard, William D., Gaínza-Lein, Marina, Glauser, Tracy A., Goldstein, Joshua L., Goodkin, Howard P., Helseth, Ashley, Kapur, Kush, McDonough, Tiffani L., Mikati, Mohamad A., Peariso, Katrina, Riviello, James, Tasker, Robert C., Topjian, Alexis A., Wainwright, Mark S., Wilfong, Angus, Williams, Korwyn, Loddenkemper, Tobias
Publicado no Neurology (2017)

Clinical profile of patients with ATP1A3 mutations in Alternating Hemiplegia of Childhood—a study of 155 patients

Por Panagiotakaki, Eleni, De Grandis, Elisa, Stagnaro, Michela, Heinzen, Erin L., Fons, Carmen, Sisodiya, Sanjay, de Vries, Boukje, Goubau, Christophe, Weckhuysen, Sarah, Kemlink, David, Scheffer, Ingrid, Lesca, Gaëtan, Rabilloud, Muriel, Klich, Amna, Ramirez-Camacho, Alia, Ulate-Campos, Adriana, Campistol, Jaume, Giannotta, Melania, Moutard, Marie-Laure, Doummar, Diane, Hubsch-Bonneaud, Cecile, Jaffer, Fatima, Cross, Helen, Gurrieri, Fiorella, Tiziano, Danilo, Nevsimalova, Sona, Nicole, Sophie, Neville, Brian, van den Maagdenberg, Arn M. J. M., Mikati, Mohamad, Goldstein, David B., Vavassori, Rosaria, Arzimanoglou, Alexis
Publicado no Orphanet J Rare Dis (2015)

Exome Sequencing Followed by Large-Scale Genotyping Fails to Identify Single Rare Variants of Large Effect in Idiopathic Generalized Epilepsy

Por Heinzen, Erin L., Depondt, Chantal, Cavalleri, Gianpiero L., Ruzzo, Elizabeth K., Walley, Nicole M., Need, Anna C., Ge, Dongliang, He, Min, Cirulli, Elizabeth T., Zhao, Qian, Cronin, Kenneth D., Gumbs, Curtis E., Campbell, C. Ryan, Hong, Linda K., Maia, Jessica M., Shianna, Kevin V., McCormack, Mark, Radtke, Rodney A., O'Conner, Gerard D., Mikati, Mohamad A., Gallentine, William B., Husain, Aatif M., Sinha, Saurabh R., Chinthapalli, Krishna, Puranam, Ram S., McNamara, James O., Ottman, Ruth, Sisodiya, Sanjay M., Delanty, Norman, Goldstein, David B.
Publicado em 2012

A Recurrent De Novo Variant in NACC1 Causes a Syndrome Characterized by Infantile Epilepsy, Cataracts, and Profound Developmental Delay

Por Schoch, Kelly, Meng, Linyan, Szelinger, Szabolcs, Bearden, David R., Stray-Pedersen, Asbjorg, Busk, Oyvind L., Stong, Nicholas, Liston, Eriskay, Cohn, Ronald D., Scaglia, Fernando, Rosenfeld, Jill A., Tarpinian, Jennifer, Skraban, Cara M., Deardorff, Matthew A., Friedman, Jeremy N., Akdemir, Zeynep Coban, Walley, Nicole, Mikati, Mohamad A., Kranz, Peter G., Jasien, Joan, McConkie-Rosell, Allyn, McDonald, Marie, Wechsler, Stephanie Burns, Freemark, Michael, Kansagra, Sujay, Freedman, Sharon, Bali, Deeksha, Millan, Francisca, Bale, Sherri, Nelson, Stanley F., Lee, Hane, Dorrani, Naghmeh, Goldstein, David B., Xiao, Rui, Yang, Yaping, Posey, Jennifer E., Martinez-Agosto, Julian A., Lupski, James R., Wangler, Michael F., Shashi, Vandana
Publicado no Am J Hum Genet (2017)

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

Por Kasperavičiūtė, Dalia, Catarino, Claudia B., Heinzen, Erin L., Depondt, Chantal, Cavalleri, Gianpiero L., Caboclo, Luis O., Tate, Sarah K., Jamnadas-Khoda, Jenny, Chinthapalli, Krishna, Clayton, Lisa M.S., Shianna, Kevin V., Radtke, Rodney A., Mikati, Mohamad A., Gallentine, William B., Husain, Aatif M., Alhusaini, Saud, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Heuser, Kjell, Amos, Leslie, Ortega, Marcos, Zumsteg, Dominik, Wieser, Heinz-Gregor, Steinhoff, Bernhard J., Krämer, Günter, Hansen, Jörg, Dorn, Thomas, Kantanen, Anne-Mari, Gjerstad, Leif, Peuralinna, Terhi, Hernandez, Dena G., Eriksson, Kai J., Kälviäinen, Reetta K., Doherty, Colin P., Wood, Nicholas W., Pandolfo, Massimo, Duncan, John S., Sander, Josemir W., Delanty, Norman, Goldstein, David B., Sisodiya, Sanjay M.
Publicado em 2010

Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes

Por Heinzen, Erin L., Radtke, Rodney A., Urban, Thomas J., Cavalleri, Gianpiero L., Depondt, Chantal, Need, Anna C., Walley, Nicole M., Nicoletti, Paola, Ge, Dongliang, Catarino, Claudia B., Duncan, John S., Kasperavičiūtė, Dalia, Tate, Sarah K., Caboclo, Luis O., Sander, Josemir W., Clayton, Lisa, Linney, Kristen N., Shianna, Kevin V., Gumbs, Curtis E., Smith, Jason, Cronin, Kenneth D., Maia, Jessica M., Doherty, Colin P., Pandolfo, Massimo, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Kälviäinen, Reetta, Eriksson, Kai, Kantanen, Anne-Mari, Dorn, Thomas, Hansen, Jörg, Krämer, Günter, Steinhoff, Bernhard J., Wieser, Heinz-Gregor, Zumsteg, Dominik, Ortega, Marcos, Wood, Nicholas W., Huxley-Jones, Julie, Mikati, Mohamad, Gallentine, William B., Husain, Aatif M., Buckley, Patrick G., Stallings, Ray L., Podgoreanu, Mihai V., Delanty, Norman, Sisodiya, Sanjay M., Goldstein, David B.
Publicado em 2010