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Items: 1 to 20 of 144

1.

Progressive dystonia.

Klein C, Münchau A.

Handb Clin Neurol. 2013;113:1889-97. doi: 10.1016/B978-0-444-59565-2.00059-9. Review.

PMID:
23622412
2.

The monogenic primary dystonias.

Müller U.

Brain. 2009 Aug;132(Pt 8):2005-25. doi: 10.1093/brain/awp172. Epub 2009 Jul 3. Review.

PMID:
19578124
3.

Overview of primary monogenic dystonia.

Spatola M, Wider C.

Parkinsonism Relat Disord. 2012 Jan;18 Suppl 1:S158-61. doi: 10.1016/S1353-8020(11)70049-9. Review.

PMID:
22166420
4.

The genetics of primary dystonias and related disorders.

Németh AH.

Brain. 2002 Apr;125(Pt 4):695-721. Review.

PMID:
11912106
5.

Nonprimary dystonias.

Dressler D.

Handb Clin Neurol. 2011;100:513-38. doi: 10.1016/B978-0-444-52014-2.00038-0. Review.

PMID:
21496605
6.

Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome.

Zimprich A, Grabowski M, Asmus F, Naumann M, Berg D, Bertram M, Scheidtmann K, Kern P, Winkelmann J, Müller-Myhsok B, Riedel L, Bauer M, Müller T, Castro M, Meitinger T, Strom TM, Gasser T.

Nat Genet. 2001 Sep;29(1):66-9.

PMID:
11528394
7.

[The varied etiologies of childhood-onset dystonia].

Roubertie A, Rivier F, Humbertclaude V, Tuffery S, Cavalier L, Cheminal R, Coubes P, Echenne B.

Rev Neurol (Paris). 2002 Apr;158(4):413-24. Review. French.

PMID:
11984483
8.

[The study and treatment of dystonias in childhood].

Pascual-Pascual SI.

Rev Neurol. 2006 Oct 10;43 Suppl 1:S161-8. Review. Spanish.

9.

Myoclonus-dystonia syndrome.

Nardocci N.

Handb Clin Neurol. 2011;100:563-75. doi: 10.1016/B978-0-444-52014-2.00041-0. Review.

PMID:
21496608
10.

Childhood dystonia.

Uc EY, Rodnitzky RL.

Semin Pediatr Neurol. 2003 Mar;10(1):52-61. Review.

PMID:
12785748
11.

Dystonia.

Morgante F, Klein C.

Continuum (Minneap Minn). 2013 Oct;19(5 Movement Disorders):1225-41. doi: 10.1212/01.CON.0000436154.08791.67. Review.

PMID:
24092288
12.

[Genetics of dystonia].

Klein C, Kann M, Kis B, Pramstaller PP, Breakefield XO, Ozelius LJ, Vieregge P.

Nervenarzt. 2000 Jun;71(6):431-41. Review. German.

PMID:
10919137
13.

[Hereditary dystonias].

Hjermind LE, Sørensen SA, Werdelin LM.

Ugeskr Laeger. 2000 Sep 18;162(38):5066-70. Review. Danish.

PMID:
11014135
14.

[New approaches in dystonia (clinical features, genetic issues and pathophysiology].

Vidailhet M, Grabli D.

Bull Acad Natl Med. 2011 Apr-May;195(4-5):921-34; discussion 934. Review. French.

PMID:
22375360
15.

Clinical and molecular genetics of primary dystonias.

Müller U, Steinberger D, Németh AH.

Neurogenetics. 1998 Mar;1(3):165-77. Review.

PMID:
10737119
16.

EFNS guidelines on diagnosis and treatment of primary dystonias.

Albanese A, Asmus F, Bhatia KP, Elia AE, Elibol B, Filippini G, Gasser T, Krauss JK, Nardocci N, Newton A, Valls-Solé J.

Eur J Neurol. 2011 Jan;18(1):5-18. doi: 10.1111/j.1468-1331.2010.03042.x.

PMID:
20482602
17.

Genetics and pharmacological treatment of dystonia.

Barrett MJ, Bressman S.

Int Rev Neurobiol. 2011;98:525-49. doi: 10.1016/B978-0-12-381328-2.00019-5. Review.

PMID:
21907099
18.

Genetics of dystonia.

Fuchs T, Ozelius LJ.

Semin Neurol. 2011 Nov;31(5):441-8. doi: 10.1055/s-0031-1299783. Epub 2012 Jan 21. Review.

PMID:
22266882
19.

Primary dystonias and genetic disorders with dystonia as clinical feature of the disease.

Moghimi N, Jabbari B, Szekely AM.

Eur J Paediatr Neurol. 2014 Jan;18(1):79-105. doi: 10.1016/j.ejpn.2013.05.015. Epub 2013 Jul 30. Review.

PMID:
23911094
20.

Primary dystonia and dystonia-plus syndromes: clinical characteristics, diagnosis, and pathogenesis.

Phukan J, Albanese A, Gasser T, Warner T.

Lancet Neurol. 2011 Dec;10(12):1074-85. doi: 10.1016/S1474-4422(11)70232-0. Epub 2011 Oct 24. Review.

PMID:
22030388

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