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Items: 1 to 20 of 427

1.

Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration.

Wolf NI, Koenig M.

Handb Clin Neurol. 2013;113:1869-78. doi: 10.1016/B978-0-444-59565-2.00057-5. Review.

PMID:
23622410
2.

Autosomal recessive cerebellar ataxias.

Palau F, Espinós C.

Orphanet J Rare Dis. 2006 Nov 17;1:47. Review.

3.

Rare forms of autosomal recessive neurodegenerative ataxia.

Koenig M.

Semin Pediatr Neurol. 2003 Sep;10(3):183-92. Review.

PMID:
14653406
4.

The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.

Di Donato S, Gellera C, Mariotti C.

Neurol Sci. 2001 Jun;22(3):219-28. Review.

PMID:
11731874
5.

Structural and functional MRI abnormalities of cerebellar cortex and nuclei in SCA3, SCA6 and Friedreich's ataxia.

Stefanescu MR, Dohnalek M, Maderwald S, Thürling M, Minnerop M, Beck A, Schlamann M, Diedrichsen J, Ladd ME, Timmann D.

Brain. 2015 May;138(Pt 5):1182-97. doi: 10.1093/brain/awv064. Epub 2015 Mar 28.

PMID:
25818870
6.

Hereditary ataxias: overview.

Jayadev S, Bird TD.

Genet Med. 2013 Sep;15(9):673-83. doi: 10.1038/gim.2013.28. Epub 2013 Mar 28. Review.

PMID:
23538602
7.

[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].

Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F.

Rev Neurol (Paris). 1991;147(12):798-808. French.

PMID:
1780608
8.

[Chronic ataxia in childhood].

Erazo Torricelli R.

Medicina (B Aires). 2013;73 Suppl 1:38-48. Review. Spanish.

9.

Molecular genetics of hereditary ataxias.

Banfi S, Zoghbi HY.

Baillieres Clin Neurol. 1994 Aug;3(2):281-95. Review.

PMID:
7952848
10.

Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective.

Koutsis G, Kladi A, Karadima G, Houlden H, Wood NW, Christodoulou K, Panas M.

J Neurol Sci. 2014 Jan 15;336(1-2):87-92. doi: 10.1016/j.jns.2013.10.012. Epub 2013 Oct 16.

PMID:
24209901
11.

[Hereditary ataxias].

Tallaksen CM.

Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1977-80. Review. Norwegian.

12.
13.

Recessive ataxia with ocular apraxia: review of 22 Portuguese patients.

Barbot C, Coutinho P, Chorão R, Ferreira C, Barros J, Fineza I, Dias K, Monteiro J, Guimarães A, Mendonça P, do Céu Moreira M, Sequeiros J.

Arch Neurol. 2001 Feb;58(2):201-5.

PMID:
11176957
14.

Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1.

Eder K, Kish SJ, Kirchgessner M, Ross BM.

Mov Disord. 1998 Sep;13(5):813-9.

PMID:
9756151
15.

Clinical and genetic aspects of spinocerebellar degeneration.

Durr A, Brice A.

Curr Opin Neurol. 2000 Aug;13(4):407-13. Review.

PMID:
10970057
16.

[Friedreich ataxia--diagnosis after a decade. Differential diagnosis of inherited spinocerebellar ataxias].

Vitaszil E, Jelencsik I, Szirmai I.

Ideggyogy Sz. 2002 Nov 20;55(11-12):382-93. Review. Hungarian.

PMID:
12632799
17.

Prevalence of inherited ataxias in the province of Padua, Italy.

Zortea M, Armani M, Pastorello E, Nunez GF, Lombardi S, Tonello S, Rigoni MT, Zuliani L, Mostacciuolo ML, Gellera C, Di Donato S, Trevisan CP.

Neuroepidemiology. 2004 Nov-Dec;23(6):275-80. Epub 2004 Aug 5.

PMID:
15297793
18.

Peripheral nerve involvement in hereditary cerebellar and multisystem degenerative disorders.

Berciano J, García A, Infante J.

Handb Clin Neurol. 2013;115:907-32. doi: 10.1016/B978-0-444-52902-2.00051-5. Review.

PMID:
23931821
19.

[Autosomal recessive cerebellar ataxias].

Anheim M.

Rev Neurol (Paris). 2011 May;167(5):372-84. doi: 10.1016/j.neurol.2010.07.021. Epub 2010 Nov 17. Review. French.

PMID:
21087783
20.

Parkinsonism & related disorders. Ataxias.

Klockgether T.

Parkinsonism Relat Disord. 2007;13 Suppl 3:S391-4. doi: 10.1016/S1353-8020(08)70036-1. Review.

PMID:
18267270

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