Works matching DE "MOVEMENT disorders"


Results: 5000
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    Nifuroxazide rescues the deleterious effects due to CHCHD10-associated MICOS defects in disease models.

    Published in:
    Brain: A Journal of Neurology, 2025, v. 148, n. 5, p. 1665, doi. 10.1093/brain/awae348
    By:
    • Ropert, Baptiste;
    • Bannwarth, Sylvie;
    • Genin, Emmanuelle C;
    • Vaillant-Beuchot, Loan;
    • Lacas-Gervais, Sandra;
    • Hounoum, Blandine Madji;
    • Bernardin, Aurore;
    • Dinh, Nhu;
    • Mauri-Crouzet, Alessandra;
    • D'Elia, Marc-Alexandre;
    • Augé, Gaelle;
    • Lespinasse, Françoise;
    • Giorgio, Audrey Di;
    • Meira, Willian;
    • Bonnefoy, Nathalie;
    • Monassier, Laurent;
    • Schiff, Manuel;
    • Sago, Laila;
    • Kilinc, Devrim;
    • Brau, Frédéric
    Publication type:
    Article
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    Real-World Use of COMT Inhibitors in the Management of Patients with Parkinson's Disease in Spain Who Present Early Motor Fluctuations: Interim Results from the REONPARK Study.

    Published in:
    Brain Sciences (2076-3425), 2025, v. 15, n. 5, p. 532, doi. 10.3390/brainsci15050532
    By:
    • López-Manzanares, Lydia;
    • García Caldentey, Juan;
    • Álvarez-Santullano, Marina Mata;
    • Vilas Rolán, Dolores;
    • Herreros-Rodríguez, Jaime;
    • Solano Vila, Berta;
    • Cerdán Sánchez, María;
    • Delgado Ballestero, Tania;
    • García-Ramos, Rocío;
    • Rodríguez-Sanz, Ana;
    • Olivares Romero, Jesús;
    • Blanco Ameijeiras, José;
    • Pijuan Jiménez, Isabel;
    • Tegel Ayuela, Iciar
    Publication type:
    Article
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    Lrrk2 pathogenic substitutions in Parkinson's disease.

    Published in:
    Neurogenetics, 2005, v. 6, n. 4, p. 171, doi. 10.1007/s10048-005-0005-1
    By:
    • Mata, Ignacio;
    • Kachergus, Jennifer;
    • Taylor, Julie;
    • Lincoln, Sarah;
    • Aasly, Jan;
    • Lynch, Timothy;
    • Hulihan, Mary;
    • Cobb, Stephanie;
    • Wu, Ruey-Meei;
    • Lu, Chin-Song;
    • Lahoz, Carlos;
    • Wszolek, Zbigniew;
    • Farrer, Matthew
    Publication type:
    Article
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    GLUT1 deficiency syndrome: a case report with a novel SLC2A1 mutation.

    Published in:
    Vojnosanitetski Pregled: Military Medical & Pharmaceutical Journal of Serbia, 2019, v. 76, n. 5, p. 543, doi. 10.2298/VSP170406120I
    By:
    • Ivančević, Nikola;
    • Cerovac, Nataša;
    • Nikolić, Blažo;
    • Čuturilo, Goran;
    • Marjanović, Ana;
    • Branković, Marija;
    • Novaković, Ivana
    Publication type:
    Article
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    Paliperidone ER-induced Tardive Dyskinesia.

    Published in:
    Klinik Psikofarmakoloji Bulteni, 2013, v. 23, n. 3, p. 264, doi. 10.5455/bcp.20130206022319
    By:
    • Yanartas, Omer;
    • Yilmaz, Yucel;
    • Saygili, Ishak;
    • Zincir, Selma Bozkurt;
    • Semiz, Umit Basar
    Publication type:
    Article
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    Vagal paraganglioma.

    Published in:
    Indian Journal of Surgery, 2006, v. 68, n. 1, p. 30
    By:
    • Tewari, M.;
    • Srivastava, V.;
    • Shukla, H. S.
    Publication type:
    Article
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