Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 14

1.

Spectrin mutations cause spinocerebellar ataxia type 5.

Ikeda Y, Dick KA, Weatherspoon MR, Gincel D, Armbrust KR, Dalton JC, Stevanin G, Dürr A, Zühlke C, Bürk K, Clark HB, Brice A, Rothstein JD, Schut LJ, Day JW, Ranum LP.

Nat Genet. 2006 Feb;38(2):184-90. Epub 2006 Jan 22.

PMID:
16429157
2.

Spinocerebellar ataxia type 5.

Dick KA, Ikeda Y, Day JW, Ranum LP.

Handb Clin Neurol. 2012;103:451-9. doi: 10.1016/B978-0-444-51892-7.00028-0. Review.

PMID:
21827906
3.

Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred.

Bürk K, Zühlke C, König IR, Ziegler A, Schwinger E, Globas C, Dichgans J, Hellenbroich Y.

Neurology. 2004 Jan 27;62(2):327-9. Review.

PMID:
14745083
4.

Spectrin mutations in spinocerebellar ataxia (SCA).

Bauer P, Schöls L, Riess O.

Bioessays. 2006 Aug;28(8):785-7. Review.

PMID:
16927298
5.

Clinical, genetic, molecular, and pathophysiological insights into spinocerebellar ataxia type 1.

Matilla-Dueñas A, Goold R, Giunti P.

Cerebellum. 2008;7(2):106-14. doi: 10.1007/s12311-008-0009-0. Review.

PMID:
18418661
6.

Spectrins: a structural platform for stabilization and activation of membrane channels, receptors and transporters.

Machnicka B, Czogalla A, Hryniewicz-Jankowska A, Bogusławska DM, Grochowalska R, Heger E, Sikorski AF.

Biochim Biophys Acta. 2014 Feb;1838(2):620-34. doi: 10.1016/j.bbamem.2013.05.002. Epub 2013 May 11. Review.

7.

[Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].

Matsuura T.

Rinsho Shinkeigaku. 2008 Jan;48(1):1-10. Review. Japanese.

PMID:
18386626
8.

[Spinocerebellar ataxia type 31].

Ishikawa K, Sato N, Niimi Y, Amino T, Mizusawa H.

Rinsho Shinkeigaku. 2010 Nov;50(11):985-7. Review. Japanese.

PMID:
21921537
9.

[Molecular and genetic analysis of spinocerebellar ataxia type 10 (SCA10)].

Matsuura T.

Rinsho Shinkeigaku. 2008 Nov;48(11):823-5. Review. Japanese.

PMID:
19198092
10.

Spinocerebellar ataxia type 11.

Giunti P, Houlden H, Gardner-Thorpe C, Worth PF, Johnson J, Hilton DA, Revesz T, Davis MB, Wood NW.

Handb Clin Neurol. 2012;103:521-34. doi: 10.1016/B978-0-444-51892-7.00033-4. Review. No abstract available.

PMID:
21827911
11.

Organizing the fluid membrane bilayer: diseases linked to spectrin and ankyrin.

Bennett V, Healy J.

Trends Mol Med. 2008 Jan;14(1):28-36. Epub 2007 Dec 20. Review.

PMID:
18083066
12.

Spinocerebellar ataxia 2 (SCA2).

Lastres-Becker I, Rüb U, Auburger G.

Cerebellum. 2008;7(2):115-24. doi: 10.1007/s12311-008-0019-y. Review.

PMID:
18418684
13.

Spectrin: structure, function and disease.

Zhang R, Zhang C, Zhao Q, Li D.

Sci China Life Sci. 2013 Dec;56(12):1076-85. doi: 10.1007/s11427-013-4575-0. Epub 2013 Dec 5. Review.

PMID:
24302288
14.

Yet another spinocerebellar ataxia--will it ever end?

Paulson H.

Lancet Neurol. 2002 Dec;1(8):471. Review. No abstract available.

PMID:
12849326
Items per page

Supplemental Content

Write to the Help Desk