Works about MOTOR neuron diseases

Results: 4260
    1
    2
    3
    4
    5

    Network analysis of the cerebrospinal fluid proteome reveals shared and unique differences between sporadic and familial forms of amyotrophic lateral sclerosis.

    Published in:
    Molecular Neurodegeneration, 2025, v. 20, n. 1, p. 1, doi. 10.1186/s13024-025-00838-9
    By:
    • Trautwig, Adam N.;
    • Fox, Edward J.;
    • Dammer, Eric B.;
    • Shantaraman, Anantharaman;
    • Ping, Lingyan;
    • Duong, Duc M.;
    • Watson, Caroline M.;
    • Wu, Fang;
    • Asress, Seneshaw;
    • Guo, Qi;
    • Levey, Allan I.;
    • Lah, James J.;
    • Verde, Federico;
    • Doretti, Alberto;
    • Ratti, Antonia;
    • Ticozzi, Nicola;
    • Ly, Cindy V.;
    • Miller, Timothy M.;
    • Garret, Mark A.;
    • Berry, James D.
    Publication type:
    Article
    6

    Intra-amniotic antisense oligonucleotide treatment improves phenotypes in preclinical models of spinal muscular atrophy.

    Published in:
    Science Translational Medicine, 2025, v. 17, n. 798, p. 1, doi. 10.1126/scitranslmed.adv4656
    By:
    • Borges, Beltran;
    • Brown, Stephen M.;
    • Chen, Wan-Jin;
    • Clarke, Maria T.;
    • Herzeg, Akos;
    • Park, Jae Hong;
    • Ross, Joshua;
    • Kong, Lingling;
    • Denton, Madeline;
    • Smith, Amy K.;
    • Lum, Tony;
    • Zada, Fareha Moulana;
    • Cordero, Marco;
    • Gupta, Nalin;
    • Cook, Sarah E.;
    • Murray, Heather;
    • Matson, John;
    • Klein, Stephanie;
    • Bennett, C. Frank;
    • Krainer, Adrian R.
    Publication type:
    Article
    7
    8
    9
    10
    11
    12
    13
    14
    15
    16
    17

    Página del Editor.

    Published in:
    Revista Mexicana de Neurociencia, 2011, v. 12, n. 4, p. 169
    By:
    • Cantú-Brito, Carlos
    Publication type:
    Article
    18
    19
    20
    21
    22
    23
    24
    25
    26
    27
    28
    29
    30
    31
    32
    33
    34
    35
    36
    37
    38

    Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations.

    Published in:
    Brain Communications, 2024, v. 6, n. 6, p. 1, doi. 10.1093/braincomms/fcae377
    By:
    • Nagy, Sara;
    • Pagnamenta, Alistair T;
    • Cali, Elisa;
    • Braakman, Hilde M H;
    • Wijntjes, Juerd;
    • Kusters, Benno;
    • Gotkine, Marc;
    • Elpeleg, Orly;
    • Meiner, Vardiella;
    • Lenberg, Jerica;
    • Wigby, Kristen;
    • Friedman, Jennifer;
    • Perry, Luke D;
    • Rossor, Alexander M;
    • Meszarosova, Anna Uhrova;
    • Thomasova, Dana;
    • Jacob, Saiju;
    • O'Driscoll, Mary;
    • Simone, Lenika De;
    • Grange, Dorothy K
    Publication type:
    Article
    39

    Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohort.

    Published in:
    Brain Communications, 2024, v. 6, n. 5, p. 1, doi. 10.1093/braincomms/fcae312
    By:
    • Abati, Elena;
    • Gagliardi, Delia;
    • Manini, Arianna;
    • Bo, Roberto Del;
    • Ronchi, Dario;
    • Meneri, Megi;
    • Beretta, Francesca;
    • Sarno, Annalisa;
    • Rizzo, Federica;
    • Monfrini, Edoardo;
    • Fonzo, Alessio Di;
    • Pellecchia, Maria Teresa;
    • Brusati, Alberto;
    • Silani, Vincenzo;
    • Comi, Giacomo Pietro;
    • Ratti, Antonia;
    • Verde, Federico;
    • Ticozzi, Nicola;
    • Corti, Stefania
    Publication type:
    Article
    40
    41

    Repeat expansions in AR, ATXN1, ATXN2 and HTT in Norwegian patients diagnosed with amyotrophic lateral sclerosis.

    Published in:
    Brain Communications, 2024, v. 6, n. 2, p. 1, doi. 10.1093/braincomms/fcae087
    By:
    • Novy, Camilla;
    • Busk, Øyvind L;
    • Tysnes, Ole-Bjørn;
    • Landa, Sigve S;
    • Aanjesen, Tori N;
    • Alstadhaug, Karl B;
    • Bjerknes, Tale L;
    • Bjørnå, Ingrid K;
    • Bråthen, Geir;
    • Dahl, Elin;
    • Demic, Natasha;
    • Fahlström, Maria;
    • Flemmen, Heidi Ø;
    • Hallerstig, Erika;
    • HogenEsch, Ineke;
    • Kampman, Margitta T;
    • Kleveland, Grethe;
    • Kvernmo, Helene B;
    • Ljøstad, Unn;
    • Maniaol, Angelina
    Publication type:
    Article
    42
    43

    Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations.

    Published in:
    Brain Communications, 2023, v. 5, n. 2, p. 1, doi. 10.1093/braincomms/fcad087
    By:
    • Wiesenfarth, Maximilian;
    • Günther, Kornelia;
    • Müller, Kathrin;
    • Witzel, Simon;
    • Weiland, Ulrike;
    • Mayer, Kristina;
    • Herrmann, Christine;
    • Brenner, David;
    • Schuster, Joachim;
    • Freischmidt, Axel;
    • Lulé, Dorothée;
    • Meyer, Thomas;
    • Regensburger, Martin;
    • Grehl, Torsten;
    • Emmer, Alexander;
    • Petri, Susanne;
    • Großkreutz, Julian;
    • Rödiger, Annekathrin;
    • Steinbach, Robert;
    • Klopstock, Thomas
    Publication type:
    Article
    44

    The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1.

    Published in:
    Brain Communications, 2023, v. 5, n. 1, p. 1, doi. 10.1093/braincomms/fcad017
    By:
    • Park, Julien H.;
    • Nordström, Ulrika;
    • Tsiakas, Konstantinos;
    • Keskin, Isil;
    • Elpers, Christiane;
    • Mannil, Manoj;
    • Heller, Raoul;
    • Nolan, Melinda;
    • Alburaiky, Salam;
    • Zetterström, Per;
    • Hempel, Maja;
    • Schara-Schmidt, Ulrike;
    • Biskup, Saskia;
    • Steinacker, Petra;
    • Otto, Markus;
    • Weishaupt, Jochen;
    • Hahn, Andreas;
    • Santer, René;
    • Marquardt, Thorsten;
    • Marklund, Stefan L.
    Publication type:
    Article
    45
    46
    47
    48

    Multicentre appraisal of amyotrophic lateral sclerosis biofluid biomarkers shows primacy of blood neurofilament light chain.

    Published in:
    Brain Communications, 2022, v. 4, n. 1, p. 1, doi. 10.1093/braincomms/fcac029
    By:
    • Thompson, Alexander G.;
    • Gray, Elizabeth;
    • Verber, Nick;
    • Bobeva, Yoana;
    • Lombardi, Vittoria;
    • Shepheard, Stephanie R.;
    • Yildiz, Ozlem;
    • Feneberg, Emily;
    • Farrimond, Lucy;
    • Dharmadasa, Thanuja;
    • Gray, Pamela;
    • Edmond, Evan C.;
    • Scaber, Jakub;
    • Gagliardi, Delia;
    • Kirby, Janine;
    • Jenkins, Thomas M.;
    • Fratta, Pietro;
    • McDermott, Christopher J.;
    • Manohar, Sanjay G.;
    • Talbot, Kevin
    Publication type:
    Article
    49
    50