Works matching DE "CEREBELLUM degeneration"

Results: 921
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    Effects of salbutamol administration on the morphology and cytoarchitecture of the cerebellum and hippocampus of adult wistar rats.

    Published in:
    Health & Research Journal, 2025, v. 11, n. 1, p. 22, doi. 10.12681/healthresj.36755
    By:
    • Popoola, AbdulGafar Niyi;
    • Ibrahim, Munirudeen;
    • Ibiyeye, Ruqayyah Yetunde;
    • Faniyi, Ayodeji Amos;
    • Balogun, Musbau Olusesan;
    • Busari, Akeem Olayinka;
    • Garba, Wasiu Olanrewaju;
    • Ogunwale, Kolawole Ayobami;
    • Lawal, Abubakar Zubair;
    • Suleiman, Ibrahim Eleha;
    • Adunmo, Godwin Olawoyin;
    • Nuhu, Abdulrazak
    Publication type:
    Article
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    Homozygous EXOSC3 Mutation c.92G→C, p.G31A is a Founder Mutation Causing Severe Pontocerebellar Hypoplasia Type 1 Among the Czech Roma.

    Published in:
    Journal of Neurogenetics, 2013, v. 27, n. 4, p. 163, doi. 10.3109/01677063.2013.814651
    By:
    • Schwabova, Jaroslava;
    • Brozkova, Dana Safka;
    • Petrak, Borivoj;
    • Mojzisova, Mahulena;
    • Pavlickova, Klara;
    • Haberlova, Jana;
    • Mrazkova, Lenka;
    • Hedvicakova, Petra;
    • Hornofova, Ludmila;
    • Kaluzova, Marie;
    • Fencl, Filip;
    • Krutova, Marcela;
    • Zamecnik, Josef;
    • Seeman, Pavel
    Publication type:
    Article
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    Pure cerebellar ataxia due to bi‐allelic PRDX3 variants including recurring p.Asp202Asn.

    Published in:
    Annals of Clinical & Translational Neurology, 2023, v. 10, n. 10, p. 1910, doi. 10.1002/acn3.51874
    By:
    • Efthymiou, Stephanie;
    • Novis, Luiz E.;
    • Koutsis, Georgios;
    • Koniari, Chrysoula;
    • Maroofian, Reza;
    • Turchetti, Valentina;
    • Velonakis, Georgios;
    • Vasconcellos, Luiz F.;
    • Raskin, Salmo;
    • Srinivasan, Varunvenkat M.;
    • Pagnamenta, Alistair T.;
    • Arun, Yaramanchanahalli B.;
    • Kinhal, Uddhava V.;
    • Gowda, Vykuntaraju K.;
    • Teive, Helio A. G.;
    • Houlden, Henry
    Publication type:
    Article
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    Impaired proteasome activity and neurodegeneration with brain iron accumulation in FBXO7 defect.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 8, p. 1436, doi. 10.1002/acn3.51095
    By:
    • Correa‐Vela, Marta;
    • Lupo, Vincenzo;
    • Montpeyó, Marta;
    • Sancho, Paula;
    • Marcé‐Grau, Anna;
    • Hernández‐Vara, Jorge;
    • Darling, Alejandra;
    • Jenkins, Alison;
    • Fernández‐Rodríguez, Sandra;
    • Tello, Cristina;
    • Ramírez‐Jiménez, Laura;
    • Pérez, Belén;
    • Sánchez‐Montáñez, Ángel;
    • Macaya, Alfons;
    • Sobrido, María J.;
    • Martinez‐Vicente, Marta;
    • Pérez‐Dueñas, Belén;
    • Espinós, Carmen
    Publication type:
    Article
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    Dystonia‐ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency.

    Published in:
    Annals of Clinical & Translational Neurology, 2020, v. 7, n. 5, p. 839, doi. 10.1002/acn3.51025
    By:
    • Ronchi, Dario;
    • Monfrini, Edoardo;
    • Bonato, Sara;
    • Mancinelli, Veronica;
    • Cinnante, Claudia;
    • Salani, Sabrina;
    • Bordoni, Andreina;
    • Ciscato, Patrizia;
    • Fortunato, Francesco;
    • Villa, Marianna;
    • Di Fonzo, Alessio;
    • Corti, Stefania;
    • Bresolin, Nereo;
    • Comi, Giacomo P.
    Publication type:
    Article
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    Impact of diabetes in the Friedreich ataxia clinical outcome measures study.

    Published in:
    Annals of Clinical & Translational Neurology, 2017, v. 4, n. 9, p. 622, doi. 10.1002/acn3.439
    By:
    • McCormick, Ashley;
    • Farmer, Jennifer;
    • Perlman, Susan;
    • Delatycki, Martin;
    • Wilmot, George;
    • Matthews, Katherine;
    • Yoon, Grace;
    • Hoyle, Chad;
    • Subramony, Sub H.;
    • Zesiewicz, Theresa;
    • Lynch, David R.;
    • McCormack, Shana E.
    Publication type:
    Article
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    The Multiple Faces of Spinocerebellar Ataxia type 2.

    Published in:
    Annals of Clinical & Translational Neurology, 2017, v. 4, n. 9, p. 687, doi. 10.1002/acn3.437
    By:
    • Antenora, Antonella;
    • Rinaldi, Carlo;
    • Roca, Alessandro;
    • Pane, Chiara;
    • Lieto, Maria;
    • Saccà, Francesco;
    • Peluso, Silvio;
    • De Michele, Giuseppe;
    • Filla, Alessandro
    Publication type:
    Article
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    Frequency of spinocerebellar ataxia mutations in patients with multiple system atrophy.

    Published in:
    Clinical Autonomic Research, 2021, v. 31, n. 1, p. 117, doi. 10.1007/s10286-020-00759-1
    By:
    • Wernick, Anna I.;
    • Walton, Ronald L.;
    • Soto-Beasley, Alexandra I.;
    • Koga, Shunsuke;
    • Heckman, Michael G.;
    • Valentino, Rebecca R.;
    • Milanowski, Lukasz M.;
    • Hoffman-Zacharska, Dorota;
    • Koziorowski, Dariusz;
    • Hassan, Anhar;
    • Uitti, Ryan J.;
    • Cheshire, William P.;
    • Singer, Wolfgang;
    • Wszolek, Zbigniew K.;
    • Dickson, Dennis W.;
    • Low, Phillip A.;
    • Ross, Owen A.
    Publication type:
    Article
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