Works matching IS 03645134 AND DT 2018 AND VI 83 AND IP 6

Results: 16

Collaborative science unites researchers and a novel spastic ataxia gene.
Published in:
2018
By:
- Fogel, Brent L.
Publication type:
journal article
Issue Information.
Published in:
Annals of Neurology, 2018, v. 83, n. 6, p. 1039, doi. 10.1002/ana.25277
Publication type:
Article
Annals of Neurology: Volume 83, Number 6, June 2018.
Published in:
Annals of Neurology, 2018, v. 83, n. 6, p. i, doi. 10.1002/ana.25275
Publication type:
Article
Repair after brainstem ischemia involves neurogenesis and the rubrospinal system.
Published in:
2018
By:
- Rüber, Theodor;
- Schlaug, Gottfried
Publication type:
journal article
Erratum.
Published in:
2018
Publication type:
journal article
Integrated magnetic resonance imaging and [<sup>11</sup> C]-PBR28 positron emission tomographic imaging in amyotrophic lateral sclerosis.
Published in:
2018
By:
- Alshikho, Mohamad J.;
- Zürcher, Nicole R.;
- Loggia, Marco L.;
- Cernasov, Paul;
- Reynolds, Beverly;
- Pijanowski, Olivia;
- Chonde, Daniel B.;
- Izquierdo Garcia, David;
- Mainero, Caterina;
- Catana, Ciprian;
- Chan, James;
- Babu, Suma;
- Paganoni, Sabrina;
- Hooker, Jacob M.;
- Atassi, Nazem
Publication type:
journal article
Randomized trial of lacosamide versus fosphenytoin for nonconvulsive seizures.
Published in:
2018
By:
- Husain, Aatif M.;
- Lee, Jong W.;
- Kolls, Bradley J.;
- Hirsch, Lawrence J.;
- Halford, Jonathan J.;
- Gupta, Puneet K.;
- Minazad, Yafa;
- Jones, Jennifer M.;
- LaRoche, Suzette M.;
- Herman, Susan T.;
- Swisher, Christa B.;
- Sinha, Saurabh R.;
- Palade, Adriana;
- Dombrowski, Keith E.;
- Gallentine, William B.;
- Hahn, Cecil D.;
- Gerard, Elizabeth E.;
- Bhapkar, Manjushri;
- Lokhnygina, Yuliya;
- Westover, M. Brandon
Publication type:
journal article
De novo gain-of-function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy.
Published in:
2018
By:
- Ambrosino, Paolo;
- Soldovieri, Maria Virginia;
- Bast, Thomas;
- Turnpenny, Peter D.;
- Uhrig, Sabine;
- Biskup, Saskia;
- Döcker, Miriam;
- Fleck, Thilo;
- Mosca, Ilaria;
- Manocchio, Laura;
- Iraci, Nunzio;
- Taglialatela, Maurizio;
- Lemke, Johannes R.
Publication type:
journal article
Prodromal symptoms of multiple sclerosis in primary care.
Published in:
2018
By:
- Disanto, Giulio;
- Zecca, Chiara;
- MacLachlan, Sharon;
- Sacco, Rosaria;
- Handunnetthi, Lahiru;
- Meier, Ute C.;
- Simpson, Alex;
- McDonald, Laura;
- Rossi, Andrea;
- Benkert, Pascal;
- Kuhle, Jens;
- Ramagopalan, Sreeram V.;
- Gobbi, Claudio
Publication type:
journal article
A probiotic modulates the microbiome and immunity in multiple sclerosis.
Published in:
2018
By:
- Tankou, Stephanie K.;
- Regev, Keren;
- Healy, Brian C.;
- Tjon, Emily;
- Laghi, Luca;
- Cox, Laura M.;
- Kivisäkk, Pia;
- Pierre, Isabelle V.;
- Hrishikesh, Lokhande;
- Gandhi, Roopali;
- Cook, Sandra;
- Glanz, Bonnie;
- Stankiewicz, James;
- Weiner, Howard L.
Publication type:
journal article
Recessive mutations in VPS13D cause childhood onset movement disorders.
Published in:
2018
By:
- Gauthier, Julie;
- Meijer, Inge A.;
- Lessel, Davor;
- Mencacci, Niccolò E.;
- Krainc, Dimitri;
- Hempel, Maja;
- Tsiakas, Konstantinos;
- Prokisch, Holger;
- Rossignol, Elsa;
- Helm, Margaret H.;
- Rodan, Lance H.;
- Karamchandani, Jason;
- Carecchio, Miryam;
- Lubbe, Steven J.;
- Telegrafi, Aida;
- Henderson, Lindsay B.;
- Lorenzo, Kerry;
- Wallace, Stephanie E.;
- Glass, Ian A.;
- Hamdan, Fadi F.
Publication type:
journal article
Feasibility, safety, and outcome of recanalization treatment in childhood stroke.
Published in:
2018
By:
- Bigi, Sandra;
- Dulcey, Andrea;
- Gralla, Jan;
- Bernasconi, Corrado;
- Melliger, Amber;
- Datta, Alexandre N.;
- Arnold, Marcel;
- Kaesmacher, Johannes;
- Fluss, Joel;
- Hackenberg, Annette;
- Maier, Oliver;
- Weber, Johannes;
- Poloni, Claudia;
- Fischer, Urs;
- Steinlin, Maja
Publication type:
journal article
Atrophy and microglial distribution in primary progressive aphasia with transactive response DNA-binding protein-43 kDa.
Published in:
2018
By:
- Kim, Garam;
- Bolbolan, Kabriya;
- Gefen, Tamar;
- Weintraub, Sandra;
- Bigio, Eileen H.;
- Rogalski, Emily;
- Mesulam, Marek‐Marsel;
- Geula, Changiz;
- Mesulam, Marek-Marsel
Publication type:
journal article
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects.
Published in:
2018
By:
- Seong, Eunju;
- Insolera, Ryan;
- Dulovic, Marija;
- Kamsteeg, Erik‐Jan;
- Trinh, Joanne;
- Brüggemann, Norbert;
- Sandford, Erin;
- Li, Sheng;
- Ozel, Ayse Bilge;
- Li, Jun Z.;
- Jewett, Tamison;
- Kievit, Anneke J. A.;
- Münchau, Alexander;
- Shakkottai, Vikram;
- Klein, Christine;
- Collins, Catherine A.;
- Lohmann, Katja;
- van de Warrenburg, Bart P.;
- Burmeister, Margit;
- Kamsteeg, Erik-Jan
Publication type:
journal article
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
Congenital Titinopathy: Comprehensive characterization and pathogenic insights.
Published in:
2018
By:
- Oates, Emily C.;
- Jones, Kristi J.;
- Donkervoort, Sandra;
- Charlton, Amanda;
- Brammah, Susan;
- Smith III, John E.;
- Ware, James S.;
- Yau, Kyle S.;
- Swanson, Lindsay C.;
- Whiffin, Nicola;
- Peduto, Anthony J.;
- Bournazos, Adam;
- Waddell, Leigh B.;
- Farrar, Michelle A.;
- Sampaio, Hugo A.;
- Teoh, Hooi Ling;
- Lamont, Phillipa J.;
- Mowat, David;
- Fitzsimons, Robin B.;
- Corbett, Alastair J.
Publication type:
journal article