Similar articles for PMID: 15824259

Year	Number of Results
1993	2
1995	1
1996	2
1997	2
1998	1
1999	4
2000	10
2001	10
2002	17
2003	14
2004	16
2005	15
2006	11
2007	10
2008	10
2009	17
2010	9
2011	8
2012	10
2013	8
2014	2
2015	6
2016	2
2017	2
2018	3
2019	2
2022	1
2024	0

1

Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.

Chen DH, Matsushita M, Rainier S, Meaney B, Tisch L, Feleke A, Wolff J, Lipe H, Fink J, Bird TD, Raskind WH. Chen DH, et al. Arch Neurol. 2005 Apr;62(4):597-600. doi: 10.1001/archneur.62.4.597. Arch Neurol. 2005. PMID: 15824259

2

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia.

Bruno MK, Lee HY, Auburger GW, Friedman A, Nielsen JE, Lang AE, Bertini E, Van Bogaert P, Averyanov Y, Hallett M, Gwinn-Hardy K, Sorenson B, Pandolfo M, Kwiecinski H, Servidei S, Fu YH, Ptácek L. Bruno MK, et al. Neurology. 2007 May 22;68(21):1782-9. doi: 10.1212/01.wnl.0000262029.91552.e0. Neurology. 2007. PMID: 17515540

3

Genetic heterogeneity in paroxysmal nonkinesigenic dyskinesia.

Spacey SD, Adams PJ, Lam PC, Materek LA, Stoessl AJ, Snutch TP, Hsiung GY. Spacey SD, et al. Neurology. 2006 May 23;66(10):1588-90. doi: 10.1212/01.wnl.0000217332.51740.7c. Neurology. 2006. PMID: 16717228

4

Myofibrillogenesis regulator 1 gene mutations cause paroxysmal dystonic choreoathetosis.

Rainier S, Thomas D, Tokarz D, Ming L, Bui M, Plein E, Zhao X, Lemons R, Albin R, Delaney C, Alvarado D, Fink JK. Rainier S, et al. Arch Neurol. 2004 Jul;61(7):1025-9. doi: 10.1001/archneur.61.7.1025. Arch Neurol. 2004. PMID: 15262732

5

Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.

Stefanova E, Djarmati A, Momcilović D, Dragasević N, Svetel M, Klein C, Kostić VS. Stefanova E, et al. Mov Disord. 2006 Nov;21(11):2010-5. doi: 10.1002/mds.21095. Mov Disord. 2006. PMID: 16972263

6

Myofibrillogenesis regulator 1 gene (MR-1) mutation in an Omani family with paroxysmal nonkinesigenic dyskinesia.

Hempelmann A, Kumar S, Muralitharan S, Sander T. Hempelmann A, et al. Neurosci Lett. 2006 Jul 10;402(1-2):118-20. doi: 10.1016/j.neulet.2006.03.048. Epub 2006 Apr 24. Neurosci Lett. 2006. PMID: 16632198

7

Familial paroxysmal nonkinesigenic dyskinesia: clinical and genetic analysis of a Taiwanese family.

Yeh TH, Lin JJ, Lai SC, Wu-Chou YH, Chen AC, Yueh KC, Chen RS, Lu CS. Yeh TH, et al. J Neurol Sci. 2012 Dec 15;323(1-2):80-4. doi: 10.1016/j.jns.2012.08.015. Epub 2012 Sep 8. J Neurol Sci. 2012. PMID: 22967746 Review.

8

Alport syndrome. Molecular genetic aspects.

Hertz JM. Hertz JM. Dan Med Bull. 2009 Aug;56(3):105-52. Dan Med Bull. 2009. PMID: 19728970

9

Paroxysmal kinesigenic dyskinesia and generalized seizures: clinical and genetic analysis in a Spanish pedigree.

Cuenca-Leon E, Cormand B, Thomson T, Macaya A. Cuenca-Leon E, et al. Neuropediatrics. 2002 Dec;33(6):288-93. doi: 10.1055/s-2002-37079. Neuropediatrics. 2002. PMID: 12571782

10

A mutation in myotilin causes spheroid body myopathy.

Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC. Foroud T, et al. Neurology. 2005 Dec 27;65(12):1936-40. doi: 10.1212/01.wnl.0000188872.28149.9a. Neurology. 2005. PMID: 16380616

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