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Items: 1 to 20 of 321

1.

Diagnosis and management of early- and late-onset cerebellar ataxia.

Brusse E, Maat-Kievit JA, van Swieten JC.

Clin Genet. 2007 Jan;71(1):12-24. Review.

PMID:
17204042
2.

[Classification and diagnosis of degenerative ataxias].

Klockgether T, Bürk K, Auburger G, Dichgans J.

Nervenarzt. 1995 Aug;66(8):571-81. Review. German.

PMID:
7566268
3.

Cerebellar/spinocerebellar syndromes.

Mariotti C, Di Donato S.

Neurol Sci. 2001 Nov;22 Suppl 2:S88-92. Review.

PMID:
11794486
4.

Autosomal recessive cerebellar ataxias.

Palau F, Espinós C.

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

5.

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 28;67(10):1769-73.

PMID:
17130408
6.

[Hereditary ataxias].

Tallaksen CM.

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

7.

[Genetic diagnosis, classification and clinical hereditary ataxia disease entities].

Schöls L, Riess O, Amoiridis G, Riess A, Przuntek H, Epplen JT.

Fortschr Neurol Psychiatr. 1997 Feb;65(2):79-89. Review. German.

PMID:
9157050
8.

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
9.

A practical approach to late-onset cerebellar ataxia: putting the disorder with lack of order into order.

van Gaalen J, van de Warrenburg BP.

Pract Neurol. 2012 Feb;12(1):14-24. doi: 10.1136/practneurol-2011-000108. Review.

PMID:
22258168
10.

[Clinical polymorphism and genetic heterogeneity of hereditary spastic ataxia].

Dadali EL, Illarioshkin SN, Markova ED, Ivanova-Smolenskaia IA.

Zh Nevropatol Psikhiatr Im S S Korsakova. 1992;92(4):10-3. Review. Russian.

PMID:
1333696
11.

Rare forms of autosomal recessive neurodegenerative ataxia.

Koenig M.

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

PMID:
14653406
12.

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
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.

[Ataxias. Diagnostic procedure and treatment].

Klockgether T.

Nervenarzt. 2005 Oct;76(10):1275-83; quiz 1284-5. Review. German.

PMID:
16175415
15.

Spinocerebellar degeneration.

Phanthumchinda K, Srikiatkachorn A.

J Med Assoc Thai. 1991 Feb;74(2):71-9.

PMID:
2056261
16.

[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
17.

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
18.

[Hereditary cerebellar ataxias: from hammer to genetics].

Arruda WO, Teive HA.

Arq Neuropsiquiatr. 1997 Sep;55(3B):666-76. Portuguese.

PMID:
9629425
19.

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
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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