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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

206 related items for PubMed ID: 35148930

  • 41.
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  • 42. Spinocerebellar ataxia type 15.
    Storey E, Gardner RJ.
    Handb Clin Neurol; 2012; 103():561-5. PubMed ID: 21827915
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  • 46. A Novel Pathogenic Variant in the SCA25-Related Gene Expanding the Etiology of Early-Onset and Progressive Cerebellar Ataxia in Childhood.
    Ferrera G, Izzo R, Ghezzi D, Nanetti L, Lamantea E, Ardissone A.
    Neuropediatrics; 2024 Apr; 55(2):135-139. PubMed ID: 37935417
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  • 47. Spinocerebellar ataxia in the Bouvier des Ardennes breed is caused by a KCNJ10 missense variant.
    Stee K, Van Poucke M, Pumarola M, Geerinckx L, Van Soens I, Bhatti SFM, Peelman L, Cornelis I.
    J Vet Intern Med; 2023 Jan; 37(1):216-222. PubMed ID: 36426918
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  • 53. Inositol 1,4,5-trisphosphate receptor type 1 autoantibody (ITPR1-IgG/anti-Sj)-associated autoimmune cerebellar ataxia, encephalitis and peripheral neuropathy: review of the literature.
    Jarius S, Bräuninger S, Chung HY, Geis C, Haas J, Komorowski L, Wildemann B, Roth C.
    J Neuroinflammation; 2022 Jul 30; 19(1):196. PubMed ID: 35907972
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  • 56. The Phenotypic Spectrum of Spinocerebellar Ataxia Type 19 in a Series of Latin American Patients.
    Avila-Jaque D, Martin F, Bustamante ML, Luna Álvarez M, Fernández JM, Dávila Ortiz de Montellano DJ, Pardo R, Varela D, Miranda M.
    Cerebellum; 2024 Aug 30; 23(4):1727-1732. PubMed ID: 38180701
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  • 59. A panel study on patients with dominant cerebellar ataxia highlights the frequency of channelopathies.
    Coutelier M, Coarelli G, Monin ML, Konop J, Davoine CS, Tesson C, Valter R, Anheim M, Behin A, Castelnovo G, Charles P, David A, Ewenczyk C, Fradin M, Goizet C, Hannequin D, Labauge P, Riant F, Sarda P, Sznajer Y, Tison F, Ullmann U, Van Maldergem L, Mochel F, Brice A, Stevanin G, Durr A, SPATAX network.
    Brain; 2017 Jun 01; 140(6):1579-1594. PubMed ID: 28444220
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