Works matching AU Mikati, Mohamad A.

Results: 60
    1
    2
    3
    4
    5
    6
    7
    8
    9

    Association of Time to Treatment With Short-term Outcomes for Pediatric Patients With Refractory Convulsive Status Epilepticus.

    Published in:
    JAMA Neurology, 2018, v. 75, n. 4, p. 410, doi. 10.1001/jamaneurol.2017.4382
    By:
    • Gaínza-Lein, Marina;
    • Sánchez Fernández, Iván;
    • Jackson, Michele;
    • Abend, Nicholas S.;
    • Arya, Ravindra;
    • Brenton, J. Nicholas;
    • Carpenter, Jessica L.;
    • Chapman, Kevin E.;
    • Gaillard, William D.;
    • Glauser, Tracy A.;
    • Goldstein, Joshua L.;
    • Goodkin, Howard P.;
    • Kapur, Kush;
    • Mikati, Mohamad A.;
    • Peariso, Katrina;
    • Tasker, Robert C.;
    • Tchapyjnikov, Dmitry;
    • Topjian, Alexis A.;
    • Wainwright, Mark S.;
    • Wilfong, Angus
    Publication type:
    Article
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19
    20
    21

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

    Published in:
    Stem Cells Translational Medicine, 2017, v. 6, n. 12, p. 2071, doi. 10.1002/sctm.17-0102
    By:
    • 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
    Publication type:
    Article
    22

    microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder.

    Published in:
    Human Molecular Genetics, 2022, v. 31, n. 17, p. 2934, doi. 10.1093/hmg/ddac085
    By:
    • Barish, Scott;
    • Senturk, Mumine;
    • Schoch, Kelly;
    • Minogue, Amanda L;
    • Lopergolo, Diego;
    • Fallerini, Chiara;
    • Harland, Jake;
    • Seemann, Jacob H;
    • Stong, Nicholas;
    • Kranz, Peter G;
    • Kansagra, Sujay;
    • Mikati, Mohamad A;
    • Jasien, Joan;
    • El-Dairi, Mays;
    • Galluzzi, Paolo;
    • Network, Undiagnosed Diseases;
    • Ariani, Francesca;
    • Renieri, Alessandra;
    • Mari, Francesca;
    • Wangler, Michael F
    Publication type:
    Article
    23
    24
    25

    Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.

    Published in:
    Brain: A Journal of Neurology, 2022, v. 145, n. 8, p. 2704, doi. 10.1093/brain/awac117
    By:
    • Lai, Dulcie;
    • Gade, Meethila;
    • Yang, Edward;
    • Koh, Hyun Yong;
    • Lu, Jinfeng;
    • Walley, Nicole M;
    • Buckley, Anne F;
    • Sands, Tristan T;
    • Akman, Cigdem I;
    • Mikati, Mohamad A;
    • McKhann, Guy M;
    • Goldman, James E;
    • Canoll, Peter;
    • Alexander, Allyson L;
    • Park, Kristen L;
    • Allmen, Gretchen K Von;
    • Rodziyevska, Olga;
    • Bhattacharjee, Meenakshi B;
    • Lidov, Hart G W;
    • Vogel, Hannes
    Publication type:
    Article
    26

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

    Published in:
    Brain: A Journal of Neurology, 2010, v. 133, n. 7, p. 2136, doi. 10.1093/brain/awq130
    By:
    • Kasperavičiūte, 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.
    Publication type:
    Article
    27

    Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy.

    Published in:
    Annals of Neurology, 2023, v. 93, n. 4, p. 752, doi. 10.1002/ana.26581
    By:
    • Perucca, Piero;
    • Stanley, Kate;
    • Harris, Natasha;
    • McIntosh, Anne M.;
    • Asadi‐Pooya, Ali A.;
    • Mikati, Mohamad A.;
    • Andrade, Danielle M.;
    • Dugan, Patricia;
    • Depondt, Chantal;
    • Choi, Hyunmi;
    • Heinzen, Erin L.;
    • Cavalleri, Gianpiero L.;
    • Buono, Russell J.;
    • Devinsky, Orrin;
    • Sperling, Michael R.;
    • Berkovic, Samuel F.;
    • Delanty, Norman;
    • Goldstein, David B.;
    • O'Brien, Terence J.;
    • Andrade, Danielle
    Publication type:
    Article
    28

    Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy.

    Published in:
    2018
    By:
    • Winawer, Melodie R.;
    • Griffin, Nicole G.;
    • Samanamud, Jorge;
    • Baugh, Evan H.;
    • Rathakrishnan, Dinesh;
    • Ramalingam, Senthilmurugan;
    • Zagzag, David;
    • Schevon, Catherine A.;
    • Dugan, Patricia;
    • Hegde, Manu;
    • Sheth, Sameer A.;
    • McKhann, Guy M.;
    • Doyle, Werner K.;
    • Grant, Gerald A.;
    • Porter, Brenda E.;
    • Mikati, Mohamad A.;
    • Muh, Carrie R.;
    • Malone, Colin D.;
    • Bergin, Ann Marie R.;
    • Peters, Jurriaan M.
    Publication type:
    journal article
    29

    Quinidine in the treatment of KCNT1-positive epilepsies.

    Published in:
    2015
    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
    Publication type:
    journal article
    30
    31
    32

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

    Published in:
    2021
    By:
    • 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;
    • de Lisle Dear, Guy;
    • Carboni, Michael P.;
    • Idriss, Salim F.;
    • Mikati, Mohamad A.;
    • Landstrom, Andrew P.;
    • Dear, Guy de Lisle
    Publication type:
    journal article
    33
    34
    35
    36
    37
    38

    Management of Landau-Kleffner Syndrome.

    Published in:
    Pediatric Drugs, 2005, v. 7, n. 6, p. 377, doi. 10.2165/00148581-200507060-00006
    By:
    • Mikati, Mohamad A.;
    • Shamseddine, Alhan N.
    Publication type:
    Article
    39
    40
    41
    42

    Time to treatment in pediatric patients with repeated episodes of status epilepticus.

    Published in:
    BMC Neurology, 2025, v. 25, n. 1, p. 1, doi. 10.1186/s12883-025-04200-w
    By:
    • Gettings, Jennifer V.;
    • Fernández, Iván Sánchez;
    • Anderson, Anne;
    • Brenton, J. Nicholas;
    • Can, Afra;
    • Clark, Justice;
    • Moeller, Raquel Farias;
    • Goodkin, Howard P.;
    • Lai, Yi-Chen;
    • Mikati, Mohamad A.;
    • Morgan, Lindsey A.;
    • Novotny, Edward;
    • Ostendorf, Adam P.;
    • Piantino, Juan;
    • Riviello, James J.;
    • Sannagowdara, Kumar;
    • Tasker, Robert C.;
    • Tchapyjnikov, Dmitry;
    • Wainwright, Mark S.;
    • Wilfong, Angus
    Publication type:
    Article
    43

    Paroxysmal Genetic Movement Disorders and Epilepsy.

    Published in:
    Frontiers in Neurology, 2021, v. 11, p. N.PAG, doi. 10.3389/fneur.2021.648031
    By:
    • de Gusmão, Claudio M.;
    • Garcia, Lucas;
    • Mikati, Mohamad A.;
    • Su, Samantha;
    • Silveira-Moriyama, Laura
    Publication type:
    Article
    44
    45
    46
    47
    48
    49

    Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain-of-function variants R201C and R201H.

    Published in:
    Epilepsia (Series 4), 2017, v. 58, n. 3, p. 436, doi. 10.1111/epi.13676
    By:
    • 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
    Publication type:
    Article
    50