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Items: 17

1.

Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1.

Flanigan K, Gardner K, Alderson K, Galster B, Otterud B, Leppert MF, Kaplan C, Ptácek LJ.

Am J Hum Genet. 1996 Aug;59(2):392-9.

2.

Rare forms of autosomal recessive neurodegenerative ataxia.

Koenig M.

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

PMID:
14653406
3.

[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
4.

Molecular genetics of hereditary ataxias.

Banfi S, Zoghbi HY.

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

PMID:
7952848
5.

[Autosomal dominant spinocerebellar ataxia].

Legros B, Manto MU.

Rev Med Brux. 1999 Dec;20(6):495-503. Review. French.

PMID:
10672773
6.

Current concepts in the treatment of hereditary ataxias.

Braga Neto P, Pedroso JL, Kuo SH, Marcondes Junior CF, Teive HA, Barsottini OG.

Arq Neuropsiquiatr. 2016 Mar;74(3):244-52. doi: 10.1590/0004-282X20160038. Review.

7.

Recent results in ataxia research.

Giunti P, Spadaro M, Colazza GB, Morocutti C.

Riv Neurol. 1991 Jul-Aug;61(4):154-7. Review.

PMID:
1815314
8.

[Molecular genetics of inherited neuropathies].

Takashima H.

Rinsho Shinkeigaku. 2006 Jan;46(1):1-18. Review. Japanese.

PMID:
16541790
9.
10.

[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
11.

Periodic vestibulocerebellar ataxia, an autosomal dominant ataxia with defective smooth pursuit, is genetically distinct from other autosomal dominant ataxias.

Damji KF, Allingham RR, Pollock SC, Small K, Lewis KE, Stajich JM, Yamaoka LH, Vance JM, Pericak-Vance MA.

Arch Neurol. 1996 Apr;53(4):338-44. Review.

PMID:
8929156
12.

[Recent progress of research on hereditary spinocerebellar degeneration].

Wakisaka A, Sasaki H.

Nihon Rinsho. 1993 Sep;51(9):2467-73. Review. Japanese.

PMID:
8411730
13.

[Spinocerebellar ataxia: advances in genetic research and its clinical implication].

Sasaki H.

Hokkaido Igaku Zasshi. 1997 Jan;72(1):13-20. Review. Japanese.

PMID:
9086358
14.

[The genetics of movement disorders--spinocerebellar degenerations].

Tallaksen CM, Dietrichs E.

Tidsskr Nor Laegeforen. 2004 Sep 9;124(17):2233-5. Review. Norwegian.

15.

Clinical aspects of hereditary ataxias.

Subramony SH.

J Child Neurol. 1995 Sep;10(5):353-62. Review.

PMID:
7499754
16.

Advances in Sequencing Technologies for Understanding Hereditary Ataxias: A Review.

Didonna A, Opal P.

JAMA Neurol. 2016 Dec 1;73(12):1485-1490. doi: 10.1001/jamaneurol.2016.3097. Review.

PMID:
27749953
17.

Spinocerebellar degenerations: an update.

Perlman SL.

Curr Neurol Neurosci Rep. 2002 Jul;2(4):331-41. Review.

PMID:
12044253

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