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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1955 1
1969 2
1970 1
1971 4
1973 2
1974 2
1975 1
1976 1
1977 1
1978 1
1979 2
1980 1
1981 2
1982 2
1983 3
1984 6
1985 1
1987 1
1988 2
1989 2
1990 1
1991 1
1992 1
1993 4
1994 3
1995 2
1996 1
1997 3
1998 2
1999 2
2000 2
2001 3
2002 2
2003 3
2004 7
2005 9
2006 11
2007 10
2008 22
2009 16
2010 5
2011 6
2012 5
2013 7
2014 3
2015 8
2016 9
2017 6
2018 5
2019 1
2020 9
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Article type
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Similar Articles for PMID: 17846221

189 results
Results by year
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Page 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 article. Review.
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
ARSACS in the Dutch population: a frequent cause of early-onset cerebellar ataxia.
Vermeer S, Meijer RP, Pijl BJ, Timmermans J, Cruysberg JR, Bos MM, Schelhaas HJ, van de Warrenburg BP, Knoers NV, Scheffer H, Kremer B. Vermeer S, et al. Neurogenetics. 2008 Jul;9(3):207-14. doi: 10.1007/s10048-008-0131-7. Epub 2008 May 9. Neurogenetics. 2008. PMID: 18465152 Free PMC article.
[Autosomal recessive spastic ataxia of Charlevoix-Saguenay: study of a family and review of the literature].
Anheim M, Chaigne D, Fleury M, Santorelli FM, De Sèze J, Durr A, Brice A, Koenig M, Tranchant C. Anheim M, et al. Rev Neurol (Paris). 2008 Apr;164(4):363-8. doi: 10.1016/j.neurol.2008.02.001. Epub 2008 Mar 25. Rev Neurol (Paris). 2008. PMID: 18439928 French.
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
A novel genomic disorder: a deletion of the SACS gene leading to spastic ataxia of Charlevoix-Saguenay.
Breckpot J, Takiyama Y, Thienpont B, Van Vooren S, Vermeesch JR, Ortibus E, Devriendt K. Breckpot J, et al. Eur J Hum Genet. 2008 Sep;16(9):1050-4. doi: 10.1038/ejhg.2008.58. Epub 2008 Apr 9. Eur J Hum Genet. 2008. PMID: 18398442 Free article.
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F. El Euch-Fayache G, et al. Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982. Arch Neurol. 2003. PMID: 12873855
Autosomal recessive spastic ataxia of Charlevoix Saguenay (ARSACS): expanding the genetic, clinical and imaging spectrum.
Synofzik M, Soehn AS, Gburek-Augustat J, Schicks J, Karle KN, Schüle R, Haack TB, Schöning M, Biskup S, Rudnik-Schöneborn S, Senderek J, Hoffmann KT, MacLeod P, Schwarz J, Bender B, Krüger S, Kreuz F, Bauer P, Schöls L. Synofzik M, et al. Orphanet J Rare Dis. 2013 Mar 15;8:41. doi: 10.1186/1750-1172-8-41. Orphanet J Rare Dis. 2013. PMID: 23497566 Free PMC article.
Cerebellar cognitive affective syndrome and autosomal recessive spastic ataxia of charlevoix-saguenay: a report of two male sibs.
Verhoeven WM, Egger JI, Ahmed AI, Kremer BP, Vermeer S, van de Warrenburg BP. Verhoeven WM, et al. Psychopathology. 2012;45(3):193-9. doi: 10.1159/000331319. Epub 2012 Mar 22. Psychopathology. 2012. PMID: 22441213
[Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance].
Ragno M, Curatola L, Rossi R, Salvolini U. Ragno M, et al. Acta Neurol (Napoli). 1992 Aug-Dec;14(4-6):431-9. Acta Neurol (Napoli). 1992. PMID: 1293986 Italian.
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