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Items: 1 to 20 of 117

1.

Case records of the Massachusetts General Hospital. Case 17-2010 - a 29-year-old woman with flexion of the left hand and foot and difficulty speaking.

Tarsy D, Sweadner KJ, Song PC.

N Engl J Med. 2010 Jun 10;362(23):2213-9. doi: 10.1056/NEJMcpc1002112. No abstract available.

PMID:
20558373
2.

ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.

Lee JY, Gollamudi S, Ozelius LJ, Kim JY, Jeon BS.

Mov Disord. 2007 Sep 15;22(12):1808-9.

PMID:
17595045
3.

Sporadic rapid-onset dystonia-parkinsonism presenting as Parkinson's disease.

Kamphuis DJ, Koelman H, Lees AJ, Tijssen MA.

Mov Disord. 2006 Jan;21(1):118-9.

PMID:
16161139
4.

Case records of the Massachusetts General Hospital. Case 26-2006. A 19-year-old woman with difficulty walking.

Venna N, Sims KB, Grant PE.

N Engl J Med. 2006 Aug 24;355(8):831-9. No abstract available.

PMID:
16928999
5.

Rapid-onset dystonia-parkinsonism: case report.

Svetel M, Ozelius LJ, Buckley A, Lohmann K, Brajković L, Klein C, Kostić VS.

J Neurol. 2010 Mar;257(3):472-4. doi: 10.1007/s00415-009-5385-y. No abstract available.

PMID:
19936820
6.

Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.

Anselm IA, Sweadner KJ, Gollamudi S, Ozelius LJ, Darras BT.

Neurology. 2009 Aug 4;73(5):400-1. doi: 10.1212/WNL.0b013e3181b04acd. No abstract available.

7.

Generalized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.

Méneret A, Mignot C, An I, Habert MO, Jacquette A, Vidailhet M, Bienvenu T, Roze E.

Mov Disord. 2012 Jan;27(1):160-1. doi: 10.1002/mds.23956. Epub 2011 Sep 23. No abstract available.

PMID:
21953941
8.

Phenomenology of "Lubag" or X-linked dystonia-parkinsonism.

Evidente VG, Advincula J, Esteban R, Pasco P, Alfon JA, Natividad FF, Cuanang J, Luis AS, Gwinn-Hardy K, Hardy J, Hernandez D, Singleton A.

Mov Disord. 2002 Nov;17(6):1271-7.

PMID:
12465067
9.

Dystonia in parkinsonian syndromes.

Albanese A.

Adv Neurol. 2003;91:351-60. Review. No abstract available.

PMID:
12442693
10.

A case of parkinsonism and dopa-induced severe dyskinesia associated with novel mutation in the GTP cyclohydrolase I gene.

Irie S, Kanazawa N, Ryoh M, Mochizuki H, Nomura Y, Segawa M.

Parkinsonism Relat Disord. 2011 Dec;17(10):769-70. doi: 10.1016/j.parkreldis.2011.06.008. Epub 2011 Jul 5. No abstract available.

PMID:
21733738
11.

Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation.

Kamm C, Fogel W, Wächter T, Schweitzer K, Berg D, Kruger R, Freudenstein D, Gasser T.

Neurology. 2008 Apr 15;70(16 Pt 2):1501-3. doi: 10.1212/01.wnl.0000310431.41036.e0. No abstract available.

PMID:
18413579
12.

Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.

Boelman C, Lagman-Bartolome AM, MacGregor DL, McCabe J, Logan WJ, Minassian BA.

Pediatr Neurol. 2014 Dec;51(6):850-3. doi: 10.1016/j.pediatrneurol.2014.08.015. Epub 2014 Aug 29.

PMID:
25439493
13.

X-linked dystonia ("Lubag") presenting predominantly with parkinsonism: a more benign phenotype?

Evidente VG, Gwinn-Hardy K, Hardy J, Hernandez D, Singleton A.

Mov Disord. 2002 Jan;17(1):200-2.

PMID:
11835466
14.

[The Na+,K+ pump continues to cause surprise].

Vilsen B.

Ugeskr Laeger. 2008 May 19;170(21):1821-3. Danish.

PMID:
18492448
15.

Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

DeAndrade MP, Yokoi F, van Groen T, Lingrel JB, Li Y.

Behav Brain Res. 2011 Jan 20;216(2):659-65. doi: 10.1016/j.bbr.2010.09.009. Epub 2010 Sep 17.

16.

The unique phenomenology of sex-linked dystonia parkinsonism (XDP, DYT3, "Lubag").

Lee LV, Rivera C, Teleg RA, Dantes MB, Pasco PM, Jamora RD, Arancillo J, Villareal-Jordan RF, Rosales RL, Demaisip C, Maranon E, Peralta O, Borres R, Tolentino C, Monding MJ, Sarcia S.

Int J Neurosci. 2011;121 Suppl 1:3-11. doi: 10.3109/00207454.2010.526728. Epub 2010 Nov 3. Review.

PMID:
21047175
17.

Heterogeneity of presentation and outcome in the Irish rapid-onset dystonia-parkinsonism kindred.

McKeon A, Ozelius LJ, Hardiman O, Greenway MJ, Pittock SJ.

Mov Disord. 2007 Jul 15;22(9):1325-7.

PMID:
17516473
18.
19.

Acral dyschromatosis with developmental regression and dystonia in a seven-year-old child: dyschromatosis symmetrica hereditaria variant or a new syndrome?

Kaliyadan F, Vinayan KP, Fernandes B, Jayasree MG.

Indian J Dermatol Venereol Leprol. 2009 Jul-Aug;75(4):412-4. doi: 10.4103/0378-6323.53154. No abstract available.

20.

Exercise-induced dystonia as a preceding symptom of familial Parkinson's disease.

Bruno MK, Ravina B, Garraux G, Hallett M, Ptacek L, Singleton A, Johnson J, Singleton A, Hanson M, Considine E, Gwinn-Hardy K.

Mov Disord. 2004 Feb;19(2):228-30.

PMID:
14978684
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