Similar articles for PMID: 17846221

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1978	1
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1992	1
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2023	2
2024	1

1

Autosomal recessive spastic ataxia of Charlevoix-Saguenay: a report of MR imaging in 5 patients.

Martin MH, Bouchard JP, Sylvain M, St-Onge O, Truchon S. Martin MH, et al. AJNR Am J Neuroradiol. 2007 Sep;28(8):1606-8. doi: 10.3174/ajnr.A0603. AJNR Am J Neuroradiol. 2007. PMID: 17846221 Free PMC article. Review.

2

Middle cerebellar peduncles and Pontine T2 hypointensities in ARSACS.

Shimazaki H, Takiyama Y, Honda J, Sakoe K, Namekawa M, Tsugawa J, Tsuboi Y, Suzuki C, Baba M, Nakano I. Shimazaki H, et al. J Neuroimaging. 2013 Jan;23(1):82-5. doi: 10.1111/j.1552-6569.2011.00647.x. Epub 2012 Jan 23. J Neuroimaging. 2013. PMID: 22268491

3

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS): novel compound heterozygous mutations in the SACS gene.

Kamada S, Okawa S, Imota T, Sugawara M, Toyoshima I. Kamada S, et al. J Neurol. 2008 Jun;255(6):803-6. doi: 10.1007/s00415-008-0672-6. Epub 2008 May 19. J Neurol. 2008. PMID: 18484239

4

Supratentorial and pontine MRI abnormalities characterize recessive spastic ataxia of Charlevoix-Saguenay. A comprehensive study of an Italian series.

Prodi E, Grisoli M, Panzeri M, Minati L, Fattori F, Erbetta A, Uziel G, D'Arrigo S, Tessa A, Ciano C, Santorelli FM, Savoiardo M, Mariotti C. Prodi E, et al. Eur J Neurol. 2013 Jan;20(1):138-46. doi: 10.1111/j.1468-1331.2012.03815.x. Epub 2012 Jul 21. Eur J Neurol. 2013. PMID: 22816526

5

A novel sacsin mutation in a Japanese woman showing clinical uniformity of autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Okawa S, Sugawara M, Watanabe S, Imota T, Toyoshima I. Okawa S, et al. J Neurol Neurosurg Psychiatry. 2006 Feb;77(2):280-2. doi: 10.1136/jnnp.2005.077297. J Neurol Neurosurg Psychiatry. 2006. PMID: 16421146 Free PMC article. No abstract available.

6

Retinal and pontine striations: neurodiagnostic signs of autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Leavitt JA, Singer W, Brown WL, Pulido JS, Brodsky MC. Leavitt JA, et al. J Neuroophthalmol. 2014 Dec;34(4):369-71. doi: 10.1097/WNO.0000000000000174. J Neuroophthalmol. 2014. PMID: 25237835

7

Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.

Ashrafi MR, Mohammadi P, Tavasoli AR, Heidari M, Hosseinpour S, Rasulinejad M, Rohani M, Akbari MG, Malamiri RA, Badv RS, Fathi D, Dehnavi AZ, Savad S, Rabbani A, Synofzik M, Mahdieh N, Rezaei Z. Ashrafi MR, et al. Cerebellum. 2023 Aug;22(4):640-650. doi: 10.1007/s12311-022-01430-3. Epub 2022 Jun 22. Cerebellum. 2023. PMID: 35731353

8

Epidemiological, clinical, paraclinical and molecular study of a cohort of 102 patients affected with autosomal recessive progressive cerebellar ataxia from Alsace, Eastern France: implications for clinical management.

Anheim M, Fleury M, Monga B, Laugel V, Chaigne D, Rodier G, Ginglinger E, Boulay C, Courtois S, Drouot N, Fritsch M, Delaunoy JP, Stoppa-Lyonnet D, Tranchant C, Koenig M. Anheim M, et al. Neurogenetics. 2010 Feb;11(1):1-12. doi: 10.1007/s10048-009-0196-y. Epub 2009 May 14. Neurogenetics. 2010. PMID: 19440741

9

Autosomal recessive spastic ataxia of Charlevoix-Saguenay.

Takiyama Y. Takiyama Y. Neuropathology. 2006 Aug;26(4):368-75. doi: 10.1111/j.1440-1789.2006.00664.x. Neuropathology. 2006. PMID: 16961075

10

Is the ataxia of Charlevoix-Saguenay a developmental disease?

Gazulla J, Vela AC, Marín MA, Pablo L, Santorelli FM, Benavente I, Modrego P, Tintoré M, Berciano J. Gazulla J, et al. Med Hypotheses. 2011 Sep;77(3):347-52. doi: 10.1016/j.mehy.2011.05.011. Epub 2011 Jun 12. Med Hypotheses. 2011. PMID: 21665375

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