Works matching IS 00068950 AND DT 2023 AND VI 146 AND IP 10

Results: 46
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    Capgras syndrome.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 3955, doi. 10.1093/brain/awad294
    By:
    • Carson, Alan
    Publication type:
    Article
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    Reducing the risks of nuclear war: the role of health professionals†.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 3953, doi. 10.1093/brain/awad269
    By:
    • Abbasi, Kamran;
    • Ali, Parveen;
    • Barbour, Virginia;
    • Bibbins-Domingo, Kirsten;
    • Rikkert, Marcel G M Olde;
    • Gong, Peng;
    • Haines, Andy;
    • Helfand, Ira;
    • Horton, Richard;
    • Mash, Bob;
    • Mitra, Arun;
    • Monteiro, Carlos;
    • Naumova, Elena N;
    • Rubin, Eric J;
    • Ruff, Tilman;
    • Sahni, Peush;
    • Tumwine, James;
    • Yonga, Paul;
    • Zielinski, Chris
    Publication type:
    Article
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    Neurologic complications in herpes simplex encephalitis: clinical, immunological and genetic studies.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4306, doi. 10.1093/brain/awad238
    By:
    • Armangué, Thaís;
    • Olivé-Cirera, Gemma;
    • Martínez-Hernandez, Eugenia;
    • Rodes, Maria;
    • Peris-Sempere, Vicente;
    • Guasp, Mar;
    • Ruiz, Raquel;
    • Palou, Eduard;
    • González, Azucena;
    • Marcos, Ma Ángeles;
    • Erro, María Elena;
    • Bataller, Luis;
    • Corral-Corral, Íñigo;
    • Planagumà, Jesus;
    • Caballero, Eva;
    • Vlagea, Alexandru;
    • Chen, Jie;
    • Bastard, Paul;
    • Materna, Marie;
    • Marchal, Astrid
    Publication type:
    Article
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    Life event.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4395, doi. 10.1093/brain/awad205
    By:
    • Lees, A J
    Publication type:
    Article
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    Genetic analysis and natural history of Charcot-Marie-Tooth disease CMTX1 due to GJB1 variants.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4336, doi. 10.1093/brain/awad187
    By:
    • Record, Christopher J;
    • Skorupinska, Mariola;
    • Laura, Matilde;
    • Rossor, Alexander M;
    • Pareyson, Davide;
    • Pisciotta, Chiara;
    • Feely, Shawna M E;
    • Lloyd, Thomas E;
    • Horvath, Rita;
    • Sadjadi, Reza;
    • Herrmann, David N;
    • Li, Jun;
    • Walk, David;
    • Yum, Sabrina W;
    • Lewis, Richard A;
    • Day, John;
    • Burns, Joshua;
    • Finkel, Richard S;
    • Saporta, Mario A;
    • Ramchandren, Sindhu
    Publication type:
    Article
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    The coming of age of liquid biopsy in neuro-oncology.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4015, doi. 10.1093/brain/awad195
    By:
    • Berzero, Giulia;
    • Pieri, Valentina;
    • Mortini, Pietro;
    • Filippi, Massimo;
    • Finocchiaro, Gaetano
    Publication type:
    Article
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    Cdc42GAP deficiency contributes to the Alzheimer's disease phenotype.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4350, doi. 10.1093/brain/awad184
    By:
    • Zhu, Mengjuan;
    • Xiao, Bin;
    • Xue, Tao;
    • Qin, Sifei;
    • Ding, Jiuyang;
    • Wu, Yue;
    • Tang, Qingqiu;
    • Huang, Mengfan;
    • Zhao, Na;
    • Ye, Yingshan;
    • Zhang, Yuning;
    • Zhang, Boya;
    • Li, Juan;
    • Guo, Fukun;
    • Jiang, Yong;
    • Zhang, Lin;
    • Zhang, Lu
    Publication type:
    Article
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    Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4077, doi. 10.1093/brain/awad183
    By:
    • Tunold, Jon-Anders;
    • Tan, Manuela M X;
    • Koga, Shunsuke;
    • Geut, Hanneke;
    • Rozemuller, Annemieke J M;
    • Valentino, Rebecca;
    • Sekiya, Hiroaki;
    • Martin, Nicholas B;
    • Heckman, Michael G;
    • Bras, Jose;
    • Guerreiro, Rita;
    • Dickson, Dennis W;
    • Toft, Mathias;
    • Berg, Wilma D J van de;
    • Ross, Owen A;
    • Pihlstrøm, Lasse
    Publication type:
    Article
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    The emerging spectrum of fetal acetylcholine receptor antibody-related disorders (FARAD).

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4233, doi. 10.1093/brain/awad153
    By:
    • Allen, Nicholas M;
    • O'Rahelly, Mark;
    • Eymard, Bruno;
    • Chouchane, Mondher;
    • Hahn, Andreas;
    • Kearns, Gerry;
    • Kim, Dae-Seong;
    • Byun, Shin Yun;
    • Nguyen, Cam-Tu Emilie;
    • Schara-Schmidt, Ulrike;
    • Kölbel, Heike;
    • Marina, Adela Della;
    • Schneider-Gold, Christiane;
    • Roefke, Kathryn;
    • Thieme, Andrea;
    • Bergh, Peter Van den;
    • Avalos, Gloria;
    • Álvarez-Velasco, Rodrigo;
    • Benito, Daniel Natera-de;
    • Cheng, Man Hin Mark
    Publication type:
    Article
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    Choroid plexus mis-splicing and altered cerebrospinal fluid composition in myotonic dystrophy type 1.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4217, doi. 10.1093/brain/awad148
    By:
    • Nutter, Curtis A;
    • Kidd, Benjamin M;
    • Carter, Helmut A;
    • Hamel, Johanna I;
    • Mackie, Philip M;
    • Kumbkarni, Nayha;
    • Davenport, Mackenzie L;
    • Tuyn, Dana M;
    • Gopinath, Adithya;
    • Creigh, Peter D;
    • Sznajder, Łukasz J;
    • Wang, Eric T;
    • Ranum, Laura P W;
    • Khoshbouei, Habibeh;
    • Day, John W;
    • Sampson, Jacinda B;
    • Prokop, Stefan;
    • Swanson, Maurice S
    Publication type:
    Article
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    Bi-allelic variants of FILIP1 cause congenital myopathy, dysmorphism and neurological defects.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4200, doi. 10.1093/brain/awad152
    By:
    • Roos, Andreas;
    • Ven, Peter F M van der;
    • Alrohaif, Hadil;
    • Kölbel, Heike;
    • Heil, Lorena;
    • Marina, Adela Della;
    • Weis, Joachim;
    • Aßent, Marvin;
    • Beck-Wödl, Stefanie;
    • Barresi, Rita;
    • Töpf, Ana;
    • O'Connor, Kaela;
    • Sickmann, Albert;
    • Kohlschmidt, Nicolai;
    • Gizouli, Magdeldin El;
    • Meyer, Nancy;
    • Daya, Nassam;
    • Grande, Valentina;
    • Bois, Karin;
    • Kaiser, Frank J
    Publication type:
    Article
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    Biallelic variants in COQ7 cause distal hereditary motor neuropathy with upper motor neuron signs.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4191, doi. 10.1093/brain/awad158
    By:
    • Rebelo, Adriana P;
    • Tomaselli, Pedro J;
    • Medina, Jessica;
    • Wang, Ying;
    • Dohrn, Maike F;
    • Nyvltova, Eva;
    • Danzi, Matt C;
    • Garrett, Mark;
    • Smith, Sean E;
    • Pestronk, Alan;
    • Li, Chengcheng;
    • Ruiz, Ariel;
    • Jacobs, Elizabeth;
    • Feely, Shawna M E;
    • França, Marcondes C;
    • Gomes, Marcus V;
    • Santos, Diogo F;
    • Kumar, Surinder;
    • Lombard, David B;
    • Saporta, Mario
    Publication type:
    Article
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    Blood transcriptome sequencing identifies biomarkers able to track disease stages in spinocerebellar ataxia type 3.

    Published in:
    Brain: A Journal of Neurology, 2023, v. 146, n. 10, p. 4132, doi. 10.1093/brain/awad128
    By:
    • Raposo, Mafalda;
    • Hübener-Schmid, Jeannette;
    • Ferreira, Ana F;
    • Melo, Ana Rosa Vieira;
    • Vasconcelos, João;
    • Pires, Paula;
    • Kay, Teresa;
    • Garcia-Moreno, Hector;
    • Giunti, Paola;
    • Santana, Magda M;
    • Almeida, Luis Pereira de;
    • Infante, Jon;
    • Warrenburg, Bart P van de;
    • Vries, Jeroen J de;
    • Faber, Jennifer;
    • Klockgether, Thomas;
    • Casadei, Nicolas;
    • Admard, Jakob;
    • Schöls, Ludger;
    • group, European Spinocerebellar ataxia type 3/Machado-Joseph disease Initiative (ESMI) study
    Publication type:
    Article
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