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autosomal dominant hereditary ataxia相关文献:
Spinocerebellar ataxia: an update.
Sullivan R, Yau WY, O'Connor E, Houlden H.
J Neurol. 2019 Feb;266(2):533-544. doi: 10.1007/s00415-018-9076-4. Epub 2018 Oct 3.
PMID:30284037
The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies.
Ruano L, Melo C, Silva MC, Coutinho P.
Neuroepidemiology. 2014;42(3):174-83. doi: 10.1159/000358801. Epub 2014 Mar 5.
PMID:24603320
Autosomal-dominant cerebellar ataxias.
Mundwiler A, Shakkottai VG.
Handb Clin Neurol. 2018;147:173-185. doi: 10.1016/B978-0-444-63233-3.00012-9.
PMID:29325610
[Hereditary Cerebellar Ataxia].
Ikeda Y.
Brain Nerve. 2025 May;77(5):469-479. doi: 10.11477/mf.188160960770050469.
PMID:40350632
Spinocerebellar ataxia 27B (SCA27B), a frequent late-onset cerebellar ataxia.
Clément G, Puisieux S, Pellerin D, Brais B, Bonnet C, Renaud M.
Rev Neurol (Paris). 2024 May;180(5):410-416. doi: 10.1016/j.neurol.2024.03.007. Epub 2024 Apr 11.
PMID:38609751
Spinocerebellar ataxias.
Soong BW, Morrison PJ.
Handb Clin Neurol. 2018;155:143-174. doi: 10.1016/B978-0-444-64189-2.00010-X.
PMID:29891056
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia-experience from an Italian cohort.
Satolli S, Rossi S, Vegezzi E, Pellerin D, Manca ML, Barghigiani M, Battisti C, Bilancieri G, Bruno G, Capacci E, Casali C, Ceravolo R, Cocozza S, Cotti Piccinelli S, Criscuolo C, Danzi MC, De Micco R, De Michele G, Dicaire MJ, Falcone GMI, Fancellu R, Ferchichi Y, Ferrari C, Filla A, Fini N, Govoni A, Lo Vecchio F, Malandrini A, Mignarri A, Musumeci O, Nesti C, Pappatà S, Pellecchia MT, Perna A, Petrucci A, Pomponi MG, Ravenni R, Ricca I, Rufa A, Tabolacci E, Tessa A, Tessitore A, Zuchner S, Silvestri G, Cortese A, Brais B, Santorelli FM.
J Neurol. 2024 Aug;271(8):5478-5488. doi: 10.1007/s00415-024-12506-x. Epub 2024 Jun 17.
PMID:38886208
Zebrafish Models of Autosomal Dominant Ataxias.
Quelle-Regaldie A, Sobrido-Cameán D, Barreiro-Iglesias A, Sobrido MJ, Sánchez L.
Cells. 2021 Feb 17;10(2):421. doi: 10.3390/cells10020421.
PMID:33671313
[Hereditary episodic ataxia].
Riant F, Vahedi K, Tournier-Lasserve E.
Rev Neurol (Paris). 2011 May;167(5):401-7. doi: 10.1016/j.neurol.2010.10.016. Epub 2011 Apr 13.
PMID:21492892
Clinical neurogenetics: autosomal dominant spinocerebellar ataxia.
Shakkottai VG, Fogel BL.
Neurol Clin. 2013 Nov;31(4):987-1007. doi: 10.1016/j.ncl.2013.04.006. Epub 2013 Jul 30.
PMID:24176420
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