641 related articles for article (PubMed ID: 24092292)
1. Cerebellar and afferent ataxias.
Pandolfo M; Manto M
Continuum (Minneap Minn); 2013 Oct; 19(5 Movement Disorders):1312-43. PubMed ID: 24092292
[TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive cerebellar ataxias.
Palau F; Espinós C
Orphanet J Rare Dis; 2006 Nov; 1():47. PubMed ID: 17112370
[TBL] [Abstract][Full Text] [Related]
3. [Hereditary ataxias].
Tallaksen CM
Tidsskr Nor Laegeforen; 2008 Sep; 128(17):1977-80. PubMed ID: 18787576
[TBL] [Abstract][Full Text] [Related]
4. [Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology].
Espinós-Armero C; González-Cabo P; Palau-Martínez F
Rev Neurol; 2005 Oct 1-15; 41(7):409-22. PubMed ID: 16193447
[TBL] [Abstract][Full Text] [Related]
5. Cerebellar ataxias.
Manto M; Marmolino D
Curr Opin Neurol; 2009 Aug; 22(4):419-29. PubMed ID: 19421057
[TBL] [Abstract][Full Text] [Related]
6. Patterns of fractional anisotropy changes in white matter of cerebellar peduncles distinguish spinocerebellar ataxia-1 from multiple system atrophy and other ataxia syndromes.
Prakash N; Hageman N; Hua X; Toga AW; Perlman SL; Salamon N
Neuroimage; 2009 Aug; 47 Suppl 2():T72-81. PubMed ID: 19446636
[TBL] [Abstract][Full Text] [Related]
7. [Clinical identification of hereditary ataxias. A study of 38 cases in Colombia].
Pedraza OL; Prieto JC; Casasbuenas OL; Espinosa E
Rev Neurol; 1997 Jul; 25(143):1016-22. PubMed ID: 9280625
[TBL] [Abstract][Full Text] [Related]
8. Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.
Gebus O; Montaut S; Monga B; Wirth T; Cheraud C; Alves Do Rego C; Zinchenko I; Carré G; Hamdaoui M; Hautecloque G; Nguyen-Them L; Lannes B; Chanson JB; Lagha-Boukbiza O; Fleury MC; Devys D; Nicolas G; Rudolf G; Bereau M; Mallaret M; Renaud M; Acquaviva C; Koenig M; Koob M; Kremer S; Namer IJ; Cazeneuve C; Echaniz-Laguna A; Tranchant C; Anheim M
J Neurol; 2017 Jun; 264(6):1118-1126. PubMed ID: 28478596
[TBL] [Abstract][Full Text] [Related]
9. [Adult-onset ataxias].
Jacobi H; Minnerop M
Nervenarzt; 2021 Apr; 92(4):379-389. PubMed ID: 33751151
[TBL] [Abstract][Full Text] [Related]
10. Dominant ataxias and Friedreich ataxia: an update.
Albin RL
Curr Opin Neurol; 2003 Aug; 16(4):507-14. PubMed ID: 12869811
[TBL] [Abstract][Full Text] [Related]
11. [Have centers of rare neurological diseases changed their practices and management of the hereditary cerebellar ataxias?].
Tranchant C
Rev Neurol (Paris); 2013 Feb; 169 Suppl 1():S23-7. PubMed ID: 23452767
[TBL] [Abstract][Full Text] [Related]
12. The inherited cerebellar ataxias: an update.
Coarelli G; Wirth T; Tranchant C; Koenig M; Durr A; Anheim M
J Neurol; 2023 Jan; 270(1):208-222. PubMed ID: 36152050
[TBL] [Abstract][Full Text] [Related]
13. Genetic cerebellar ataxias.
Storey E
Semin Neurol; 2014 Jul; 34(3):280-92. PubMed ID: 25192506
[TBL] [Abstract][Full Text] [Related]
14. [Chronic ataxia in childhood].
Erazo Torricelli R
Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
[TBL] [Abstract][Full Text] [Related]
15. [Peripheral neuropathies associated with hereditary cerebellar ataxias].
Anheim M; Tranchant C
Rev Neurol (Paris); 2011 Jan; 167(1):72-6. PubMed ID: 21195440
[TBL] [Abstract][Full Text] [Related]
16. Recessive cerebellar and afferent ataxias - clinical challenges and future directions.
Beaudin M; Manto M; Schmahmann JD; Pandolfo M; Dupre N
Nat Rev Neurol; 2022 May; 18(5):257-272. PubMed ID: 35332317
[TBL] [Abstract][Full Text] [Related]
17. Differences in saccade dynamics between spinocerebellar ataxia 2 and late-onset cerebellar ataxias.
Federighi P; Cevenini G; Dotti MT; Rosini F; Pretegiani E; Federico A; Rufa A
Brain; 2011 Mar; 134(Pt 3):879-91. PubMed ID: 21354979
[TBL] [Abstract][Full Text] [Related]
18. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
Le Ber I; Clot F; Vercueil L; Camuzat A; Viémont M; Benamar N; De Liège P; Ouvrard-Hernandez AM; Pollak P; Stevanin G; Brice A; Dürr A
Neurology; 2006 Nov; 67(10):1769-73. PubMed ID: 17130408
[TBL] [Abstract][Full Text] [Related]
19. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature.
Bhidayasiri R; Perlman SL; Pulst SM; Geschwind DH
Arch Neurol; 2005 Dec; 62(12):1865-9. PubMed ID: 16344344
[TBL] [Abstract][Full Text] [Related]
20. Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.
Gros-Louis F; Dupré N; Dion P; Fox MA; Laurent S; Verreault S; Sanes JR; Bouchard JP; Rouleau GA
Nat Genet; 2007 Jan; 39(1):80-5. PubMed ID: 17159980
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
