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Items: 1 to 20 of 185

1.

Bilateral deep brain stimulation of the pallidum for myoclonus-dystonia due to ε-sarcoglycan mutations: a pilot study.

Azoulay-Zyss J, Roze E, Welter ML, Navarro S, Yelnik J, Clot F, Bardinet E, Karachi C, Dormont D, Galanaud D, Pidoux B, Cornu P, Vidailhet M, Grabli D.

Arch Neurol. 2011 Jan;68(1):94-8. doi: 10.1001/archneurol.2010.338.

PMID:
21220679
2.

Effect of pallidal deep brain stimulation on psychiatric symptoms in myoclonus-dystonia due to ε-sarcoglycan mutations.

Contarino MF, Foncke EM, Cath DC, Schuurman PR, Speelman JD, Tijssen MA.

Arch Neurol. 2011 Aug;68(8):1087-8; author reply 1088-9. doi: 10.1001/archneurol.2011.180. No abstract available.

PMID:
21825253
3.

Bilateral globus pallidus interna deep-brain stimulation in a patient with myoclonus-dystonia: a case report.

Kim JH, Na YC, Lee WH, Chang WS, Jung HH, Chang JW.

Neuromodulation. 2014 Dec;17(8):724-8. doi: 10.1111/ner.12162. Epub 2014 Feb 25.

PMID:
24612290
4.

Bilateral pallidal stimulation for sargoglycan epsilon negative myoclonus.

Sidiropoulos C, Mestre T, Hutchison W, Moro E, Valencia A, Poon YY, Fallis M, Rughani AI, Kalia SK, Lozano AM, Lang AE.

Parkinsonism Relat Disord. 2014 Aug;20(8):915-8. doi: 10.1016/j.parkreldis.2014.04.017. Epub 2014 Apr 24.

PMID:
24812007
5.

Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes.

Tezenas du Montcel S, Clot F, Vidailhet M, Roze E, Damier P, Jedynak CP, Camuzat A, Lagueny A, Vercueil L, Doummar D, Guyant-Maréchal L, Houeto JL, Ponsot G, Thobois S, Cournelle MA, Durr A, Durif F, Echenne B, Hannequin D, Tranchant C, Brice A; French Dystonia Network.

J Med Genet. 2006 May;43(5):394-400. Epub 2005 Oct 14.

6.

Myoclonus-dystonia due to genomic deletions in the epsilon-sarcoglycan gene.

Asmus F, Salih F, Hjermind LE, Ostergaard K, Munz M, Kühn AA, Dupont E, Kupsch A, Gasser T.

Ann Neurol. 2005 Nov;58(5):792-7.

PMID:
16240355
7.

Pallidal and thalamic deep brain stimulation in myoclonus-dystonia.

Gruber D, Kühn AA, Schoenecker T, Kivi A, Trottenberg T, Hoffmann KT, Gharabaghi A, Kopp UA, Schneider GH, Klein C, Asmus F, Kupsch A.

Mov Disord. 2010 Aug 15;25(11):1733-43. doi: 10.1002/mds.23312.

PMID:
20623686
8.

Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria.

Carecchio M, Magliozzi M, Copetti M, Ferraris A, Bernardini L, Bonetti M, Defazio G, Edwards MJ, Torrente I, Pellegrini F, Comi C, Bhatia KP, Valente EM.

Mov Disord. 2013 Jun;28(6):787-94. doi: 10.1002/mds.25506. Epub 2013 May 15.

PMID:
23677909
9.

Unusual familial presentation of epsilon-sarcoglycan gene mutation with falls and writer's cramp.

Koukouni V, Valente EM, Cordivari C, Bhatia KP, Quinn NP.

Mov Disord. 2008 Oct 15;23(13):1913-5. doi: 10.1002/mds.21935.

PMID:
18702114
10.

Deep brain stimulation of the internal globus pallidus for refractory tardive dystonia.

Cohen OS, Hassin-Baer S, Spiegelmann R.

Parkinsonism Relat Disord. 2007 Dec;13(8):541-4. Epub 2007 Jan 19.

PMID:
17236806
11.

Pediatric writer's cramp in myoclonus-dystonia: maternal imprinting hides positive family history.

Gerrits MC, Foncke EM, Koelman JH, Tijssen MA.

Eur J Paediatr Neurol. 2009 Mar;13(2):178-80. doi: 10.1016/j.ejpn.2008.03.007. Epub 2008 Jun 20.

PMID:
18571946
12.

Focal brain glucose hypermetabolism in myoclonus-dystonia syndrome caused by an epsilon-sarcoglycan gene mutation.

Tai CH, Yen RF, Lin CH, Yen KY, Yip PK, Wu RM, Lee MJ.

Parkinsonism Relat Disord. 2009 Sep;15(8):614-6. doi: 10.1016/j.parkreldis.2008.11.007. Epub 2009 Mar 3. No abstract available.

PMID:
19261534
13.

Analysis of the epsilon-sarcoglycan gene in familial and sporadic myoclonus-dystonia: evidence for genetic heterogeneity.

Valente EM, Misbahuddin A, Brancati F, Placzek MR, Garavaglia B, Salvi S, Nemeth A, Shaw-Smith C, Nardocci N, Bentivoglio AR, Berardelli A, Eleopra R, Dallapiccola B, Warner TT.

Mov Disord. 2003 Sep;18(9):1047-51.

PMID:
14502674
14.

Deep brain stimulation in myoclonus-dystonia syndrome.

Cif L, Valente EM, Hemm S, Coubes C, Vayssiere N, Serrat S, Di Giorgio A, Coubes P.

Mov Disord. 2004 Jun;19(6):724-7.

PMID:
15197720
15.

Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.

Asmus F, Zimprich A, Tezenas Du Montcel S, Kabus C, Deuschl G, Kupsch A, Ziemann U, Castro M, Kühn AA, Strom TM, Vidailhet M, Bhatia KP, Dürr A, Wood NW, Brice A, Gasser T.

Ann Neurol. 2002 Oct;52(4):489-92.

PMID:
12325078
16.

Thalamic Vo-complex vs pallidal deep brain stimulation for focal hand dystonia.

Goto S, Shimazu H, Matsuzaki K, Tamura T, Murase N, Nagahiro S, Kaji R.

Neurology. 2008 Apr 15;70(16 Pt 2):1500-1. doi: 10.1212/01.wnl.0000310430.00743.11. No abstract available.

PMID:
18413578
17.

Deep brain stimulation of the internal globus pallidus in dystonia: target localisation under general anaesthesia.

Pinsker MO, Volkmann J, Falk D, Herzog J, Steigerwald F, Deuschl G, Mehdorn HM.

Acta Neurochir (Wien). 2009 Jul;151(7):751-8. doi: 10.1007/s00701-009-0375-5. Epub 2009 May 26.

PMID:
19468677
18.

Clinical and neurophysiological improvement of SGCE myoclonus-dystonia with GPi deep brain stimulation.

Kurtis MM, San Luciano M, Yu Q, Goodman RR, Ford B, Raymond D, Pullman SL, Saunders-Pullman R.

Clin Neurol Neurosurg. 2010 Feb;112(2):149-52. doi: 10.1016/j.clineuro.2009.10.001. Epub 2009 Nov 5.

19.

The epsilon-sarcoglycan gene in myoclonic syndromes.

Valente EM, Edwards MJ, Mir P, DiGiorgio A, Salvi S, Davis M, Russo N, Bozi M, Kim HT, Pennisi G, Quinn N, Dallapiccola B, Bhatia KP.

Neurology. 2005 Feb 22;64(4):737-9.

PMID:
15728306
20.

Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias.

Grundmann K, Laubis-Herrmann U, Dressler D, Vollmer-Haase J, Bauer P, Stuhrmann M, Schulte T, Schöls L, Topka H, Riess O.

Mov Disord. 2004 Nov;19(11):1294-7.

PMID:
15390016

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